US20040086884A1 - Methods and compositions for RNA interference - Google Patents

Abstract

The present invention provides methods for attenuating gene expression in a cell using gene-targeted double stranded RNA (dsRNA). The dsRNA contains a nucleotide sequence that hybridizes under physiologic conditions of the cell to the nucleotide sequence of at least a portion of the gene to be inhibited (the “target” gene).

Description

RELATED APPLICATIONS
• This application is a continuation-in-part of U.S. application Ser. No. 10/055,797, filed Jan. 22, 2002, which is a continuation-in-part of International Application PCT/US01/08435, filed Mar. 16, 2001, which claims the benefit of priority from U.S. Provisional Application Nos. 60/189,739, filed Mar. 16, 2000, and 60/243,097, filed Oct. 24, 2000. This application is also a continuation-in-part of U.S. application Ser. No. 09/866,557 filed May 24, 2001 and a continuation-in-part of U.S. application Ser. No. 09/858,862 filed May 16, 2001. The specifications of such applications are incorporated by reference herein. International Application PCT/US01/08435 was published under PCT Article 21(2) in English.[0001]
GOVERNMENT SUPPORT
• [0002] Work described herein was supported by National Institutes of Health Grant R01-GM62534. The United States Government may have certain rights in the invention.
BACKGROUND OF THE INVENTION
• “RNA interference”, “post-transcriptional gene silencing”, “quelling”—these different names describe similar effects that result from the overexpression or misexpression of transgenes, or from the deliberate introduction of double-stranded RNA into cells (reviewed in Fire A (1999) Trends Genet 15: 358-363; Sharp P A (1999)[0003]Genes Dev13: 139-141; Hunter C (1999)Curr Biol9: R440-R442; Baulcombe D C (1999)Curr Biol9: R599-R601; Vaucheret et al. (1998)Plant J16: 651-659). The injection of double-stranded RNA into the nematodeCaenorhabditis elegans, for example, acts systemically to cause the post-transcriptional depletion of the homologous endogenous RNA (Fire et al. (1998)Nature391: 806-811; and Montgomery et al. (1998)PNAS95: 15502-15507). RNA interference, commonly referred to as RNAi, offers a way of specifically and potently inactivating a cloned gene, and is proving a powerful tool for investigating gene function. Although the phenomenon is interesting in its own right; the mechanism has been rather mysterious, but recent research—for example that recently reported by Smardon et al. (2000)Curr Biol10: 169-178—is beginning to shed light on the nature and evolution of the biological processes that underlie RNAi.
• RNAi was discovered when researchers attempting to use the antisense RNA approach to inactivate a[0004]C. elegansgene found that injection of sense-strand RNA was actually as effective as the antisense RNA at inhibiting gene function (Guo et al. (1995)Cell81: 611-620). Further investigation revealed that the active agent was modest amounts of double-stranded RNA that contaminate in vitro RNA preparations. Researchers quickly determined the ‘rules’ and effects of RNAi which have become the paradigm for thinking about the mechanism which mediates this affect. Exon sequences are required, whereas introns and promoter sequences, while ineffective, do not appear to compromise RNAi (though there may be gene-specific exceptions to this rule). RNAi acts systemically—injection into one tissue inhibits gene function in cells throughout the animal. The results of a variety of experiments, inC. elegansand other organisms, indicate that RNAi acts to destabilize cellular RNA after RNA processing.
• The potency of RNAi inspired Timmons and Fire (1998[0005]Nature395: 854) to do a simple experiment that produced an astonishing result. They fed to nematodes bacteria that had been engineered to express double-stranded RNA corresponding to theC. elegansunc-22 gene. Amazingly, these nematodes developed a phenotype similar to that of unc-22 mutants that was dependent on their food source. The ability to conditionally expose large numbers of nematodes to gene-specific double-stranded RNA formed the basis for a very powerful screen to select for RNAi-defectiveC. elegansmutants and then to identify the corresponding genes.
• Double-stranded RNAs (dsRNAs) can provoke gene silencing in numerous in vivo contexts including Drosophila,[0006]Caenorhabditis elegans, planaria, hydra, trypanosomes, fungi and plants. However, the ability to recapitulate this phenomenon in higher eukaryotes, particularly mammalian cells, has not been accomplished in the art. Nor has the prior art demonstrated that this phenomena can be observed in cultured eukaryotic cells. Additionally, the ‘rules’ established by the prior art have taught that RNAi requires exon sequences, and thus constructs consisting of intronic or promoter sequences were not believed to be effective reagents in mediating RNAi. The present invention aims to address each of these deficiencies in the prior art and provides evidence both that RNAi can be observed in cultured eukaryotic cells and that RNAi constructs consisting of non-exon sequences can effectively repress gene expression.
SUMMARY OF THE INVENTION
• One aspect of the present invention provides a method for attenuating expression of a target gene in cultured cells, comprising introducing double stranded RNA (dsRNA) into the cells in an amount sufficient to attenuate expression of the target gene, wherein the dsRNA comprises a nucleotide sequence that hybridizes under stringent conditions to a nucleotide sequence of the target gene.[0007]
• Another aspect of the present invention provides a method for attenuating expression of a target gene in a mammalian cell, comprising[0008]
• (i) activating one or both of a Dicer activity or an Argonaut activity in the cell, and[0009]
• (ii) introducing into the cell a double stranded RNA (dsRNA) in an amount sufficient to attenuate expression of the target gene, wherein the dsRNA comprises a nucleotide sequence that hybridizes under stringent conditions to a nucleotide sequence of the target gene.[0010]
• In certain embodiments, the cell is suspended in culture; while in other embodiments the cell is in a whole animal, such as a non-human mammal.[0011]
• In certain preferred embodiments, the cell is engineered with (i) a recombinant gene encoding a Dicer activity, (ii) a recombinant gene encoding an Argonaut activity, or (iii) both. For instance, the recombinant gene may encode, for a example, a protein which includes an amino acid sequence at least 50 percent identical to SEQ ID No. 2 or 4; or be defined by a coding sequence which hybridizes under wash conditions of 2×SSC at 22° C. to SEQ ID No. 1 or 3. In certain embodiments, the recombinant gene may encode, for a example, a protein which includes an amino acid sequence at least 50 percent identical to the Argonaut sequence shown in FIG. 24. In certain embodiments, the recombinant gene may encode a protein which includes an amino acid sequence at least 60 percent, 70 percent, 80 percent, 85 percent, 90 percent, or 95 percent identical to SEQ ID No. 2 or 4. In certain embodiments, the recombinant gene may be defined by a coding sequence which hybridizes under stringent conditions, including a wash step selected from 0.2×-2.0×SSC at from 50° C.-65° C., to SEQ ID No. 1 or 3.[0012]
• In certain embodiments, rather than use a heterologous expression construct(s), an endogenous Dicer gene or Argonaut gene can be activated, e.g., by gene activation technology, expression of activated transcription factors or other signal transduction protein(s), which induces expression of the gene, or by treatment with an endogenous factor which upregulates the level of expression of the protein or inhibits the degradation of the protein.[0013]
• In certain preferred embodiments, the target gene is an endogenous gene of the cell. In other embodiments, the target gene is a heterologous gene relative to the genome of the cell, such as a pathogen gene, e.g., a viral gene.[0014]
• In certain embodiments, the cell is treated with an agent that inhibits protein kinase RNA-activated (PKR) apoptosis, such as by treatment with agents which inhibit expression of PKR, cause its destruction, and/or inhibit the kinase activity of PKR.[0015]
• In certain preferred embodiments, the cell is a primate cell, such as a human cell.[0016]
• In certain preferred embodiments, the length of the dsRNA is at least 20, 21 or 22 nucleotides in length, e.g., corresponding in size to RNA products produced by Dicer-dependent cleavage. In certain embodiments, the dsRNA construct is at least 25, 50, 100, 200, 300 or 400 bases. In certain embodiments, the dsRNA construct is 400-800 bases in length.[0017]
• In certain preferred embodiments, expression of the target gene is attenuated by at least 5 fold, and more preferably at least 10, 20 or even 50 fold, e.g., relative to the untreated cell or a cell treated with a dsRNA construct which does not correspond to the target gene.[0018]
• Yet another aspect of the present invention provides a method for attenuating expression of a target gene in cultured cells, comprising introducing an expression vector having a “coding sequence” which, when transcribed, produces double stranded RNA (dsRNA) in the cell in an amount sufficient to attenuate expression of the target gene, wherein the dsRNA comprises a nucleotide sequence that hybridizes under stringent conditions to a nucleotide sequence of the target gene. In certain embodiments, the vector includes a single coding sequence for the dsRNA which is operably linked to (two) transcriptional regulatory sequences which cause transcription in both directions to form complementary transcripts of the coding sequence. In other embodiments, the vector includes two coding sequences which, respectively, give rise to the two complementary sequences which form the dsRNA when annealed. In still other embodiments, the vector includes a coding sequence which forms a hairpin. In certain embodiments, the vectors are episomal, e.g., and transfection is transient. In other embodiments, the vectors are chromosomally integrated, e.g., to produce a stably transfected cell line. Preferred vectors for forming such stable cell lines are described in U.S. Pat. No. 6,025,192 and PCT publication WO/9812339, which are incorporated by reference herein.[0019]
• Another aspect of the present invention provides a method for attenuating expression of a target gene in cultured cells, comprising introducing an expression vector having a “non-coding sequence” which, when transcribed, produces double stranded RNA (dsRNA) in the cell in an amount sufficient to attenuate expression of the target gene. The non-coding sequence may include intronic or promoter sequence of the target gene of interest, and the dsRNA comprises a nucleotide sequence that hybridizes under stringent conditions to a nucleotide sequence of the promoter or intron of the target gene. In certain embodiments, the vector includes a single sequence for the dsRNA which is operably linked to (two) transcriptional regulatory sequences which cause transcription in both directions to form complementary transcripts of the sequence. In other embodiments, the vector includes two sequences which, respectively, give rise to the two complementary sequences which form the dsRNA when annealed. In still other embodiments, the vector includes a coding sequence which forms a hairpin. In certain embodiments, the vectors are episomal, e.g., and transfection is transient. In other embodiments, the vectors are chromosomally integrated, e.g., to produce a stably transfected cell line. Preferred vectors for forming such stable cell lines are described in U.S. Pat. No. 6,025,192 and PCT publication WO/9812339, which are incorporated by reference herein.[0020]
• Another aspect the present invention provides a double stranded (ds) RNA for inhibiting expression of a mammalian gene. The dsRNA comprises a first nucleotide sequence that hybridizes under stringent conditions, including a wash step of 0.2×SSC at 65° C., to a nucleotide sequence of at least one mammalian gene and a second nucleotide sequence which is complementary to the first nucleotide sequence.[0021]
• In one embodiment, the first nucleotide sequence of said double-stranded RNA is at least 20, 21, 22, 25, 50, 100, 200, 300, 400, 500, 800 nucleotides in length.[0022]
• In another embodiment, the first nucleotide sequence of said double-stranded RNA is identical to at least one mammalian gene. In another embodiment, the first nucleotide sequence of said double-stranded RNA is identical to one mammalian gene. In yet another embodiment, the first nucleotide sequence of said double-stranded RNA hybridizes under stringent conditions to at least one human gene. In still another embodiment, the first nucleotide sequence of said double-stranded RNA is identical to at least one human gene. In still another embodiment, the first nucleotide sequence of said double-stranded RNA is identical to one human gene.[0023]
• The double-stranded RNA may be an siRNA or a hairpin, and may be expressed transiently or stably. In one embodiment, the double-stranded RNA is a hairpin comprising a first nucleotide sequence that hybridizes under stringent conditions to a nucleotide sequence of at least one mammalian gene, and a second nucleotide sequence which is a complementary inverted repeat of said first nucleotide sequence and hybridizes to said first nucleotide sequence to form a hairpin structure.[0024]
• The first nucleotide sequence of said double-stranded RNA can hybridize to either coding or non-coding sequence of at least one mammalian gene. In one embodiment, the first nucleotide sequence of said double-stranded RNA hybridizes to a coding sequence of at least one mammalian gene. In another embodiment, the first nucleotide sequence of said double-stranded RNA hybridizes to a coding sequence of at least one human gene. In another embodiment, the first nucleotide sequence of said double-stranded RNA is identical to a coding sequence of at least one mammalian gene. In still another embodiment, the first nucleotide sequence of said double-stranded RNA is identical to a coding sequence of at least one human gene.[0025]
• In another embodiment, the first nucleotide sequence of said double-stranded RNA hybridizes to a non-coding sequence of at least one mammalian gene. In another enbodiment, the first nucleotide sequence of said double-stranded RNA hybridizes to a non-coding sequence of at least one human gene. In another embodiment, the first nucleotide sequence of said double-stranded RNA is identical to a non-coding sequence of at least one mammalian gene. In still another embodiment, the first nucleotide sequence of said double-stranded RNA is identical to a non-coding sequence of at least one human gene. In any of the foregoing embodiments, the non-coding sequence may be a non-transcribed sequence.[0026]
• Still another aspect of the present invention provides an assay for identifying nucleic acid sequences, either coding or non-coding sequences, responsible for conferring a particular phenotype in a cell, comprising[0027]
• (i) constructing a variegated library of nucleic acid sequences from a cell in an orientation relative to a promoter to produce double stranded DNA;[0028]
• (ii) introducing the variegated dsRNA library into a culture of target cells;[0029]
• (iii) identifying members of the library which confer a particular phenotype on the cell, and identifying the sequence from a cell which correspond, such as being identical or homologous, to the library member.[0030]
• Yet another aspect of the present invention provides a method of conducting a drug discovery business comprising:[0031]
• (i) identifying, by the subject assay, a target gene which provides a phenotypically desirable response when inhibited by RNAi;[0032]
• (ii) identifying agents by their ability to inhibit expression of the target gene or the activity of an expression product of the target gene;[0033]
• (iii) conducting therapeutic profiling of agents identified in step (b), or further analogs thereof, for efficacy and toxicity in animals; and[0034]
• (iv) formulating a pharmaceutical preparation including one or more agents identified in step (iii) as having an acceptable therapeutic profile.[0035]
• The method may include an additional step of establishing a distribution system for distributing the pharmaceutical preparation for sale, and may optionally include establishing a sales group for marketing the pharmaceutical preparation.[0036]
• Another aspect of the present invention provides a method of conducting a target discovery business comprising:[0037]
• (i) identifying, by the subject assay, a target gene which provides a phenotypically desirable response when inhibited by RNAi;[0038]
• (ii) (optionally) conducting therapeutic profiling of the target gene for efficacy and toxicity in animals; and[0039]
• (iii) licensing, to a third party, the rights for further drug development of inhibitors of the target gene.[0040]
• Another aspect of the invention provides a method for inhibiting RNAi by inhibiting the expression or activity of an RNAi enzyme. Thus, the subject method may include inhibiting the activity of Dicer and/or the 22-mer RNA.[0041]
• Still another aspect relates to a method for altering the specificity of an RNAi by modifying the sequence of the RNA component of the RNAi enzyme.[0042]
• In another aspect, gene expression in an undifferentiated stem cell, or the differentiated progeny thereof, is altered by introducing dsRNA of the present invention. In one embodiment, the stem cells are embryonic stem cells. Preferably, the embryonic stem cells are derived from mammals, more preferably from non-human primates, and most preferably from humans.[0043]
• The embryonic stem cells may be isolated by methods known to one of skill in the art from the inner cell mass (ICM) of blastocyst stage embryos. In one embodiment the embryonic stem cells are obtained from previously established cell lines. In a second embodiment, the embryonic stem cells are derived de novo by standard methods.[0044]
• In another aspect, the embryonic stem cells are the result of nuclear transfer. The donor nuclei are obtained from any adult, fetal, or embryonic tissue by methods well known in the art. In one embodiment, the donor nuclei is transferred to a recipient oocyte which had previously been modified. In one embodiment, the oocyte is modified using one or more dsRNAs. Exemplary modifications of the recipient oocyte include any changes in gene or protein expression that prevent an embryo derived from said modified oocyte from successfully implanting in the uterine wall. Since implantation in the uterine wall is essential for fertilized mammalian embryos to progress from beyond the blastocyst stage, embryos made from such modified oocytes could not give rise to viable organisms. Non-limiting examples of such modifications include those that decrease or eliminate expression of cell surface receptors (i.e., integrins) required for the recognition between the blastocyst and the uterine wall, modifications that decrease or eliminate expression of proteases (i.e., collagenase, stromelysin, and plasminogen activator) required to digest matrix in the uterine lining and thus allow proper implantation, and modifications that decrease or eliminate expression of proteases (i.e., strypsin) necessary for the blastocyst to hatch from the zona pellucida. Such hatching is required for implantation.[0045]
• In another embodiment, embryonic stem cells, embryonic stem cells obtained from fertilization of modified oocytes, or the differentiated progeny thereof, can be modified or further modified with one or more dsRNAs. In a preferred embodiment, the modification decreases or eliminates MHC expression. Cells modified in this way will be tolerated by the recipient, thus avoiding complications arising from graft rejection. Such modified cells are suitable for transplantation into a related or unrelated patient to treat a condition characterized by cell damage or cell loss.[0046]
• In another aspect of the invention, the undifferentiated stem cell is an adult stem cell. Exemplary adult stem cells include, but are not limited to, hematopoietic stem cells, mesenchymal stem cells, cardiac stem cells, pancreatic stem cells, and neural stem cells. Exemplary adult stem cells include any stem cell capable of forming differentiated ectodermal, mesodermal, or endodermal derivatives. Non-limiting examples of differentiated cell types which arise from adult stem cells include: blood, skeletal muscle, myocardium, endocardium, pericardium, bone, cartilage, tendon, ligament, connective tissue, adipose tissue, liver, pancreas, skin, neural tissue, lung, small intestine, large intestine, gall bladder, rectum, anus, bladder, female or male reproductive tract, genitals, and the linings of the body cavity.[0047]
• In one embodiment, an undifferentiated adult stem cell, or the differentiated progeny thereof, is altered with one or more dsRNAs to decrease or eliminate MHC expression. Cells modified in this way will be tolerated by the recipient, thus avoiding complications arising from graft rejection. Such modified cells are suitable for transplantation into a related or unrelated patient to treat a condition characterized by cell damage or cell loss.[0048]
• In another aspect of the invention, an embryonic stem cell, an undifferentiated adult stem cell, or the differentiated progeny of either an embryonic or adult stem cell is altered with one or more dsRNA to decrease or eliminate expression of genes required for HIV infection. In a preferred embodiment, the stem cell is one capable of giving rise to hematopoietic cells. Modified cells with hematopoietic potential can be transplanted into a patient as a preventative therapy or treatment for HIV or AIDS.[0049]
• Another aspect of the invention relates to purified or semi-purified preparations of the RNAi enzyme or components thereof. In certain embodiments, the preparations are used for identifying compounds, especially small organic molecules, which inhibit or potentiate the RNAi activity. Small molecule inhibitors, for example, can be used to inhibit dsRNA responses in cells which are purposefully being transfected with a virus which produces double stranded RNA.[0050]
• The dsRNA construct may comprise one or more strands of polymerized ribonucleotide. It may include modifications to either the phosphate-sugar backbone or the nucleoside. The double-stranded structure may be formed by a single self-complementary RNA strand or two complementary RNA strands. RNA duplex formation may be initiated either inside or outside the cell. The dsRNA construct may be introduced in an amount which allows delivery of at least one copy per cell. Higher doses of double-stranded material may yield more effective inhibition. Inhibition is sequence-specific in that nucleotide sequences corresponding to the duplex region of the RNA are targeted for genetic inhibition. In certain embodiments, dsRNA constructs containing a nucleotide sequences identical to a portion of the target gene are preferred for inhibition. RNA sequences with insertions, deletions, and single point mutations relative to the target sequence (i.e., RNA sequences similar to the target sequence) have also been found to be effective for inhibition. Thus, sequence identity may be optimized by alignment algorithms known in the art and calculating the percent difference between the nucleotide sequences. Alternatively, the duplex region of the RNA may be defined functionally as a nucleotide sequence that is capable of hybridizing with a portion of the target gene transcript. In another embodiment, dsRNA constructs containing nucleotide sequences identical to a non-coding portion of the target gene are preferred for inhibition. Exemplary non-coding regions include introns and the promoter region. Sequences with insertions, deletions, and single point mutations relative to the target non-coding sequence may also be used.[0051]
• Yet another aspect of the invention pertains to transgenic non-human mammals which include a transgene encoding a dsRNA construct, wherein the dsRNA is identical or similar to either the coding or non-coding sequence of the target gene, preferably which is stably integrated into the genome of cells in which it occurs. The animals can be derived by oocyte microinjection, for example, in which case all of the nucleated cells of the animal will include the transgene, or can be derived using embryonic stem (ES) cells which have been transfected with the transgene, in which case the animal is a chimera and only a portion of its nucleated cells will include the transgene. In certain instances, the sequence-independent dsRNA response, e.g., the PKR response, is also inhibited in those cells including the transgene.[0052]
• In still other embodiments, dsRNA itself can be introduced into an ES cell in order to effect gene silencing, and that phenotype will be carried for at least several rounds of division, e.g., into the progeny of that cell.[0053]
BRIEF DESCRIPTION OF THE DRAWINGS
• FIG. 1: RNAi in S2 cells. (a) Drosophila S2 cells were transfected with a plasmid that directs lacZ expression from the copia promoter in combination with dsRNAs corresponding to either human CD8 or lacZ, or with no dsRNA, as indicated. (b) S2 cells were co-transfected with a plasmid that directs expression of a GFP-US9 fusion protein and dsRNAs of either lacZ or cyclin E, as indicated. Upper panels show FACS profiles of the bulk population. Lower panels show FACS profiles from GFP-positive cells. (c) Total RNA was extracted from cells transfected with lacZ, cyclin E, fizzy or cyclin A dsRNAs, as indicated. Northern blots were hybridized with sequences not present in the transfected dsRNAs.[0054]
• FIG. 2: RNAi in vitro. (a) Transcripts corresponding to either the first 600 nucleotides of Drosophila cyclin E (E600) or the first 800 nucleotides of lacZ (Z800) were incubated in lysates derived from cells that had been transfected with either lacZ or cyclin E (cycE) dsRNAs, as indicated. Time points were 0, 10, 20, 30, 40 and 60 min for cyclin E and 0, 10, 20, 30 and 60 min for lacZ. (b) Transcripts were incubated in an extract of S2 cells that had been transfected with cyclin E dsRNA (cross-hatched box, below). Transcripts corresponded to the first 800 nucleotides of lacZ or the first 600, 300, 220 or 100 nucleotides of cyclin E, as indicated. Eout is a transcript derived from the portion of the cyclin E cDNA not contained within the transfected dsRNA. E-ds is identical to the dsRNA that had been transfected into S2 cells. Time points were 0 and 30 min. (c) Synthetic transcripts complementary to the complete cyclin E cDNA (Eas) or the final 600 nucleotides (Eas600) or 300 nucleotides (Eas300) were incubated in extract for 0 or 30 min.[0055]
• FIG. 3: Substrate requirements of the RISC. Extracts were prepared from cells transfected with cyclin E dsRNA. Aliquots were incubated for 30 min at 30° C. before the addition of either the cyclin E (E600) or lacZ (Z800) substrate.[0056]Individual 20 μl aliquots, as indicated, were pre-incubated with 1 mM CaCl₂and 5 mM EGTA, 1 mM CaCl₂, 5 mM EGTA and 60 U of micrococcal nuclease, 1 mM CaCl₂and 60 U of micrococcal nuclease or 10 U of DNase I (Promega) and 5 mM EGTA. After the 30 min pre-incubation, EGTA was added to those samples that lacked it. Yeast tRNA (1 μg) was added to all samples. Time points were at 0 and 30 min.
• FIG. 4: The RISC contains a potential guide RNA. (a) Northern blots of RNA from either a crude lysate or the S100 fraction (containing the soluble nuclease activity, see Methods) were hybridized to a riboprobe derived from the sense strand of the cyclin E mRNA. (b) Soluble cyclin-E-specific nuclease activity was fractionated as described in Methods. Fractions from the anion-exchange resin were incubated with the lacZ, control substrate (upper panel) or the cyclin E substrate (centre panel). Lower panel, RNA from each fraction was analysed by northern blotting with a uniformly labelled transcript derived from sense strand of the cyclin E cDNA. DNA oligonucleotides were used as size markers.[0057]
• FIG. 5: Generation of 22mers and degradation of mRNA are carried out by distinct enzymatic complexes. (a) Extracts prepared either from 0-12 hour Drosophila embryos or Drosophila S2 cells (see Methods) were incubated for 0, 15, 30, or 60 minutes (left to right) with a uniformly-labeled double-stranded RNA corresponding to the first 500 nucleotides of the Drosophila cyclin E coding region. M indicates a marker prepared by in vitro transcription of a synthetic template. The template was designed to yield a 22 nucleotide transcript. The doublet most probably results from improper initiation at the +1 position. (b) Whole-cell extracts were prepared from S2 cells that had been transfected with a dsRNA corresponding to the first 500 nt. of the luciferase coding region. S10 extracts were spun at 30,000×g for 20 minutes which represents our standard RISC extract. S100 extracts were prepared by further centrifugation of S10 extracts for 60 minutes at 100,000×g. Assays for mRNA degradation were carried out as described previously for 0, 30 or 60 minutes (left to right in each set) with either a single-stranded luciferase mRNA or a single-stranded cyclin E mRNA, as indicated. (c) S10 or S100 extracts were incubated with cyclin E dsRNAs for 0, 60 or 120 minutes (L to R).[0058]
• FIG. 6: Production of 22mers by recombinant CG4792/Dicer. (a) Drosophila S2 cells were transfected with plasmids that direct the expression of T7-epitope tagged versions of Drosha, CG4792/Dicer-1 and Homeless. Tagged proteins were purified from cell lysates by immunoprecipitation and were incubated with cyclin E dsRNA. For comparison, reactions were also performed in Drosophila embryo and S2 cell extracts. As a negative control, immunoprecipitates were prepared from cells transfected with a β-galactosidase expression vector. Pairs of lanes show reactions performed for 0 or 60 minutes. The synthetic marker (M) is as described in the legend to FIG. 1. (b) Diagrammatic representations of the domain structures of CG4792/Dicer-1, Drosha and Homeless are shown. (c) Immunoprecipitates were prepared from detergent lysates of S2 cells using an antiserum raised against the C-[0059]terminal 8 amino acids of Drosophila Dicer-1 (CG4792). As controls, similar preparations were made with a pre-immune serum and with an immune serum that had been pre-incubated with an excess of antigenic peptide. Cleavage reactions in which each of these precipitates was incubated with an ˜500 nt. fragment of Drosophila cyclin E are shown. For comparsion, an incubation of the substrate in Drosophila embryo extract was electrophoresed in parallel. (d) Dicer immunoprecipitates were incubated with dsRNA substrates in the presence or absence of ATP. For comparison, the same substrate was incubated with S2 extracts that either contained added ATP or that were depleted of ATP using glucose and hexokinase (see methods). (e) Drosophila S2 cells were transfected with uniformly,³²P-labelled dsRNA corresponding to the first 500 nt. of GFP. RISC complex was affinity purified using a histidine-tagged version of Drosophila Ago-2, a recently identified component of the RISC complex (Hammond et al., in prep). RISC was isolated either under conditions in which it remains ribosome associated (ls, low salt) or under conditions that extract it from the ribosome in a soluble form (hs, high salt). For comparison, the spectrum of labelled RNAs in the total lysate is shown. (f) Guide RNAs produced by incubation of dsRNA with a Dicer immunoprecipitate are compared to guide RNAs present in an affinity-purified RISC complex. These precisely comigrate on a gel that has single-nucleotide resolution. The lane labelled control is an affinity selection for RISC from a cell that had been transfected with labeled dsRNA but not with the epitope-tagged Drosophila Ago-2.
• FIG. 7: Dicer participates in RNAi. (a) Drosophila S2 cells were transfected with dsRNAs corresponding to the two Drosophila Dicers (CG4792 and CG6493) or with a control dsRNA corresponding to murine caspase 9. Cytoplasmic extracts of these cells were tested for Dicer activity. Transfection with Dicer dsRNA reduced activity in lysates by 7.4-fold. (b) The Dicer-1 antiserum (CG4792) was used to prepare immunoprecipitates from S2 cells that had been treated as described above. Dicer dsRNA reduced the activity of Dicer-1 in this assay by 6.2-fold. (c) Cells that had been transfected two days previously with either mouse caspase 9 dsRNA or with Dicer dsRNA were cotransfected with a GFP expression plasmid and either control, luciferase dsRNA or GFP dsRNA. Three independent experiments were quantified by FACS. A comparison of the relative percentage of GFP-positive cells is shown for control (GFP plasmid plus luciferase dsRNA) or silenced (GFP plamsid plus GFP dsRNA) populations in cells that had previously been transfected with either control (caspase 9) or Dicer dsRNAs.[0060]
• FIG. 8: Dicer is an evolutionarily conserved ribonuclease. (a) A model for production of 22mers by Dicer. Based upon the proposed mechanism of action of Ribonuclease III, we propose that Dicer acts on its substrate as a dimer. The positioning of the two ribonuclease domains (RIIIa and RIIIb) within the enzyme would thus determine the size of the cleavage product. An equally plausible alternative model could be derived in which the RIIIa and RIIIb domains of each Dicer enzyme would cleave in concert at a single position. In this model, the size of the cleavage product would be determined by interaction between two neighboring Dicer enzymes. (b) Comparison of the domain structures of potential Dicer homologs in various organisms (Drosophila—CG4792, CG6493,[0061]C. elegans—K12H4.8, Arabidopsis—CARPEL FACTORY, T25K16.4,AC012328_—1, human Helicase-MOI andS. pombe—YC9A_SCHPO). The ZAP domains were identified both by analysis of individual sequences with Pfam and by Psi-blast searches. The ZAP domain in the putativeS. pombeDicer is not detected by PFAM but is identified by Psi-Blast and is thus shown in a different color. For comparison, a domain structure of the RDE1/QDE2/ARGONAUTE family is shown. It should be noted that the ZAP domains are more similar within each of the Dicer and ARGONAUTE families than they are between the two groups. (c) An alignment of the ZAP domains in selected Dicer and Argonaute family members is shown. The alignment was produced using ClustalW.
• FIG. 9: Purification strategy for RISC. (second step in RNAi model).[0062]
• FIG. 10: Fractionation of RISC activity over sizing column. Activity fractionates as 500 KDa complex. Also, antibody to[0063]Drosophila argonaute 2 cofractionates with activity.
• FIGS.[0064]11-13: Fractionation of RISC over monoS, monoQ, Hydroxyapatite columns.Drosophila argonaute 2 protein also cofactionates.
• FIG. 14: Alignment of Drosophila argonaute 2 with other family members.[0065]
• FIG. 15: Confirmation of[0066]Drosophila argonaute 2. S2 cells were transfected with labeled dsRNA and His tagged argonaute. Argonaute was isolated on nickel agarose and RNA component was identified on 15% acrylamide gel.
• FIG. 16: S2 cell and embryo extracts were assayed for 22mer generating activity.[0067]
• FIG. 17: RISC can be separated from 22mer generating activity (dicer). Spinning extracts (S100) can clear RISC activity from supernatant (left panel) however, S100 spins still contain dicer activity (right panel).[0068]
• FIG. 18: Dicer is specific for dsRNA and prefers longer substrates.[0069]
• FIG. 19: Dicer was fractionated over several columns.[0070]
• FIG. 20: Identification of dicer as enzyme which can process dsRNA into 22mers. Various RNaseIII family members were expressed with n terminal tags, immunoprecipitated, and assayed for 22mer generating activity (left panel). In right panel, antibodies to dicer could also precipitate 22mer generating activity.[0071]
• FIG. 21: Dicer requires ATP.[0072]
• FIG. 22: Dicer produces RNAs that are the same size as RNAs present in RISC.[0073]
• FIG. 23: Human dicer homolog when expressed and immunoprecipitated has 22mer generating activity.[0074]
• FIG. 24: Sequence of[0075]Drosophila argonaute 2. Peptides identified by microsequencing are shown in underline.
• FIG. 25: Molecular charaterization of[0076]Drosophila argonaute 2. The presence of an intron in coding sequence was determined by northern blotting using intron probe. This results in a different 5′ reading frame then the published genome seqeunce. Number of polyglutamine repeats was determined by genomic PCR.
• FIG. 26: Dicer activity can be created in human cells by expression of human dicer gene. Host cell was 293. Crude extracts had dicer activity, while activity was absent from untransfected cells. Activity is not dissimilar to that seen in drosophila embryo extracts.[0077]
• FIG. 27: A ˜500 nt. fragment of the gene that is to be silenced (X) is inserted into the modified vector as a stable direct repeat using standard cloning procedures. Treatment with commercially available cre recombinase reverses sequences within the loxP sites (L) to create an inverted repeat. This can be stably maintained and amplified in an sbc mutant bacterial strain (DL759). Transcription in vivo from the promoter of choice (P) yields a hairpin RNA that causes silencing. A zeocin resistance marker is included to insure maintenance of the direct and inverted repeat structures; however this is non-essential in vivo and could be removed by pre-mRNA splicing if desired. (Smith et al. (2000)[0078]Nature407: 319-20).
• FIG. 28: RNAi in P19 embryonal carcinoma cells. Ten-centimeter plates of P19 cells were transfected by using 5 μg of GFP plasmid and 40 μg of the indicated dsRNA (or no RNA). Cells were photographed by fluorescent (tope panel) and phase-contrast microscopy (bottom panel) at 72 h after transfection; silencing was also clearly evident at 48 h posttransfection.[0079]
• FIG. 29: RNAi of firefly and Renilla luciferase in P19 cells. (A and B) P19 cells were transfected with plasmids that direct the expression of firefly and Renilla luciferase and[0080]dsRNA 500 mers (25 or 250 ng, as indicated in A and B, respectively), that were either homologous to the firefly luciferase mRNA (dsFF) or nonhomologous (dsGFP). Luciferase activities were assayed at various times after transfection, as indicated. Ratios of firefly to Renilla activity are normalized to dsGFP controls. (C and D) P19 cells in 12-well culture dishes (2 ml of media) were transfected with 0.25 μg of a 9:1 mix of pGL3-Control and pRL-SV40 as well as 2 μg of the indicated RNA. Extracts were prepared 9 h after transfection. (C) Ratio of firefly to Renilla luciferase is shown. (D) Ratio of Renilla to firefly luciferase is shown. Values are normalized to dsGFP. The average of three independent experiments is shown; error bars indicate standard deviation.
• FIG. 30: The panels at the right show expression of either RFP or GFP following transient transfection into wild type P19 cells. The panels at the left demonstrate the specific suppression of GFP expression in P19 clones which stably express a 500 nt double stranded GFP hairpin. P19 clones which stably express the double stranded GFP hairpin were transiently transfected with RFP or GFP, and expression of RFP or GFP was assessed by visual inspection.[0081]
• FIG. 31: Specific silencing of luciferase expression by dsRNA in murine embryonic stem cells. Mouse embryonic stem cells in 12-well culture dishes (1 ml of media) were transfected with 1.5 μg of dsRNA along with 0.25 μg of a 10:1 mixture of the reporter plasmids pGL3-Control and pRL-SV40. Extracts were prepared and assayed 20 h after transfection. The ratio of firefly to Renilla luciferase expression is shown for FF ds500; the ratio of Renilla to firefly is shown for Ren ds500. Both are normalized to ratios from the dsGFP transfection. The average of three independent experiments is shown; error bars indicate standard deviation.[0082]
• FIG. 32: RNAi in C2C12 murine myoblast cells. (A) Mouse C2C12-cells in 12-well culture dishes (1 ml of media) were transfected with 1 μg of the indicated dsRNA along with 0.250 μg of the reporter plasmids pGL3-Control and pRL-SV40. Extracts were prepared and assayed 24 h after transfection. The ratio of firefly to Renilla luciferase expression is shown; values are normalized to ratios from the no dsRNA control. The average of three independent experiments is shown; error bars indicate standard deviation. (B) C2C12 cells cotransfected with 1 μg of either plasmid alone or a plasmid containing a hyperactive mutant of vaccinia virus K3L (Kawagishi-Kobayashi et al. 2000, Virology 276: 424-434). The absolute counts of Renilla and firefly luciferase activity are shown. (C) The ratios of firefly/Renilla activity from B, normalized to no dsRNA controls.[0083]
• FIG. 33: Hela, Chinese hamster ovary, and P19 (pluripotent, mouse embryonic carcinoma) cell lines transfected with plasmids expressing[0084]Photinus pyralis(firefly) andRenilla reniformis(sea pansy) luciferases and with dsRNA 500mers (400 ng), homologous to either firefly luciferase mRNA (dsLUC) or non-homologous (dsGFP). Dual luciferase assays were carried out using an Analytical Scientific Instruments model 3010 Luminometer. In this assay Renilla luciferase serves as an internal control for dsRNA-specific suppression of firefly luciferase activity. These data demonstrate that 500mer dsRNA can specifically suppress cognate gene expression in vivo.
• FIG. 34: Expression of a hairpin RNA produces P19 EC cell lines that stably silence GFP. (A) A cartoon of the FLIP cassette used to construct the GFP hairpin. GFP represents the first 500 coding base pairs of EGFP. Zeo, zeocin resistance gene; L, Lox; P, the cytomegalovirus promoter in the expression plasmid pcDNA3. Homologous GFP fragments are first cloned as direct repeats into the FLIP cassette. To create inverted repeats for hairpin production, the second repeat is flipped by using Cre recombinase. When transcribed, the inverted repeat forms a GFP dsRNA with a hairpin loop. (B) P19 cell lines stably expressing the GFP hairpin plasmid, GFPhp.1 (clone 10) and GFPhp.2 (clone 12), along with wt P19 were transfected with 0.25 μg each of GFP and RFP reporter genes. Fluorescence micrographs were taken by using filters appropriate for GFP and RFP. Magnification is 200×. (C) P19 GFPhp.1 cells were transfected with pEGFP and 0, 0.5, or 1 μg of Dicer or firefly dsRNA. Fluorescence micrographs were taken at 48 h posttransfection and are superimposed with bright field images to reveal non-GFP expressing cells. Magnification is 100×. (D) In vitro and in vivo processing of dsRNA in P19 cells. In vitro Dicer assays were performed on S2 cells and three independently prepared P19 extracts by using[0085]³²P-labeled dsRNA (30° C. for 30 min). A Northern blot of RNA extracted from control and GFPhp.1 P19 cells shows the production of ≈22mer RNA species in hairpin-expressing cells but not in control cells. Blots were probed with a³²P-labeled “sense” GFP transcript.
• FIG. 35: dsRNA induces silencing at the posttranscriptional level. P19 cell extracts were used for in vitro translation of firefly and Renilla luciferase mRNA (100 ng each). Translation reactions were programmed with various amounts of dsRNA 500mers, either homologous to firefly luciferase mRNA (dsLUC) or nonhomologous (dsGFP). Luciferase assays were carried out after a 1 h incubation at 30° C. Ratios of firefly to Renilla activity are normalized to no dsRNA controls. Standard deviations from the mean are shown.[0086]
• FIG. 36: S10 fractions from P19 cell lysates were used for in vitro translations of mRNA coding for[0087]Photinus pyralis(firefly) andRenilla reniformis(sea pansy) luciferases. Translation reactions were programmed with dsRNA, ssRNA, or asRNA 500mers, either complementary to firefly luciferase mRNA (dsFF, ssFF, or asFF), complementary to Renilla luciferase (dsREN, ssREN, or asREN) or non-complementary (dsGFP). Reactions were carried out at 30° C. for 1 hour, after a 30 min preincubation with dsRNA, ssRNA, or asRNA. Dual luciferase assays were carried out using an Analytical Scientific Instruments model 3010 Luminometer. On the left, Renilla luciferase serves as an internal control for dsRNA-specific suppression of firefly luciferase activity. On the right, firefly luciferase serves as an internal control for dsRNA-specific suppression of Renilla luciferase activity. These data demonstrate that 500mer double-stranded RNA (dsRNA) but not single-stranded (ssRNA) or anti-sense RNA (asRNA) suppresses cognate gene expression in vitro in a manner consistent with post-transcriptional gene silencing.
• FIG. 37: P19 cells were grown in 6-well tissue culture plates to approximately 60% confluence. Various amounts of dsRNA, either homologous to firefly luciferase mRNA (dsLUC) or non-homologous (dsGFP), were added to each well and incubated for 12 hrs under normal tissue culture conditions. Cells were then transfected with plasmids expressing[0088]Photinus pyralis(firefly) andRenilla reniformis(sea pansy) luciferases and with dsRNA 500mers (500 ng). Dual luciferase assays were carried out 12 hrs post-transfection using an Analytical Scientific Instruments model 3010 Luminometer. In this assay Renilla luciferase serves as an internal control for dsRNA-specific suppression of firefly luciferase activity. These data show that 500mer dsRNA can specifically suppress cognate gene expression in vivo without transfection under normal tissue culture conditions.
• FIG. 38: Previous methods for generating siRNAs required costly chemical synthesis. The invention provides an in vitro method for synthesizing siRNAs using standard RNA transcription reactions.[0089]
• FIG. 39: Short hairpins suppress gene expression in Drosophila S2 cells. (A) Sequences and predicted secondary structure of representative chemically synthesized RNAs. Sequences correspond to positions 112-134 (siRNA) and 463-491 (shRNAs) of Firefly luciferase carried on pGL3-Control. An siRNA targeted to position 463-485 of the luciferase sequence was virtually identical to the 112-134 siRNA in suppressing expression, but is not shown. (B) Exogenously supplied short hairpins suppress expression of the targeted Firefly luciferase gene in vivo. Six-well plates of S2 cells were transfected with 250 ng/well of plasmids that direct the expression of firefly and Renilla luciferase and 500 ng/well of the indicated RNA. Luciferase activities were assayed 48 h after transfection. Ratios of firefly to Renilla luciferase activity were normalized to a control transfected with an siRNA directed at the green fluorescent protein (GFP). The average of three independent experiments is shown; error bars indicate standard deviation. (C) Short hairpins are processed by the Drosophila Dicer enzyme. T7 transcribed hairpins shFfL22, shFfL29, and shFfS29 were incubated with (+) and without (−) 0-2-h Drosophila embryo extracts. Those incubated with extract produced ˜22-nt siRNAs, consistent with the ability of these hairpins to induce RNA interference. A long dsRNA input (cyclin E 500-mer) was used as a control. Cleavage reactions were performed as described in Bernstein et al., 2001, Nature, 409:363-366.[0090]
• FIG. 40: Short hairpins function in mammalian cells.[0091]HEK 293T, HeLa, COS-1, and NIH 3T3 cells were transfected with plasmids and RNAs as in FIG. 1 and subjected to dual luciferase assays 48 h posttransfection. The ratios of firefly to Renilla luciferase activity are normalized to a control transfected with an siRNA directed at the green fluorescent protein (GFP). The average of three independent experiments is shown; error bars indicate standard deviation.
• FIG. 41: siRNAs and short hairpins transcribed in vitro suppress gene expression in mammalian cells. (A) Sequences and predicted secondary structure of representative in vitro transcribed siRNAs. Sequences correspond to positions 112-134 (siRNA) and 463-491 (shRNAs) of firefly luciferase carried on pGL3-Control. (B) In vitro transcribed siRNAs suppress expression of the targeted firefly luciferase gene in vivo.[0092]HEK 293T cells were transfected with plasmids as in FIG. 2. The presence of non-base-paired guanosine residues at the 5′ end of siRNAs significantly alters the predicted end structure and abolishes siRNA activity. (C) Sequences and predicted secondary structure of representative in vitro transcribed shRNAs. Sequences correspond to positions 112-141 of firefly luciferase carried on pGL3-Control. (D) Short hairpins transcribed in vitro suppress expression of the targeted firefly luciferase gene in vivo.HEK 293T cells were transfected with plasmids as in FIG. 2.
• FIG. 42: Transcription of functional shRNAs in vivo. (A) Schematic of the pShh1 vector. Sequences encoding shRNAs with between 19 and 29 bases of homology to the targeted gene are synthesized as 60-75-bp double-stranded DNA oligonucleotides and ligated into an EcoRV site immediately downstream of the U6 promoter. (B) Sequence and predicted secondary structure of the Ff1 hairpin. (C) An shRNA expressed from the pShh1 vector suppresses luciferase expression in mammalian cells.[0093]HEK 293T, HeLa, COS-1, and NIH 3T3 cells were transfected with reporter plasmids as in FIG. 1, and pShh1 vector, firefly siRNA, or pshh1 firefly shRNA constructs as indicated. The ratios of firefly to Renilla luciferase activity were determined 48 h after transfection and represent the average of three independent experiments; error bars indicate standard deviation.
• FIG. 43: Dicer is required for shRNA-mediated gene silencing.[0094]HEK 293T cells were transfected with luciferase reporter plasmids as well as pShh1-Ff1 and an siRNA targeting human Dicer either alone or in combination, as indicated. The Dicer siRNA sequence (TCA ACC AGC CAC TGC TGG A) corresponds to coordinates 3137-3155 of the human Dicer sequence. The ratios of firefly to Renilla luciferase activity were determined 26 h after transfection and represent the average of three independent experiments; error bars indicate standard deviation.
• FIG. 44: Stable shRNA-mediated gene silencing of an endogenous gene. (A) Sequence and predicted secondary structure of the p53 hairpin. The 5′ shRNA stem contains a 27-nt sequence derived from mouse p53 (nucleotides 166-192), whereas the 3′ stem harbors the complimentary antisense sequence. (B) Senescence bypass in primary mouse embryo fibroblasts (MEFs) expressing an shRNA targeted at p53. Wild-type MEFs,[0095]passage 5, were transfected with pBabe-RasV12 with control plasmid or with p53hp (5 μg each with FuGENE; Roche). Two days after transfection, cells were trypsinized, counted, and plated at a density of 1×10⁵/10-cm plate in media containing 2.0 μg/mL of puromycin. Control cells cease proliferation and show a senescent morphology (left panel). Cells expressing the p53 hairpin continue to grow (right panel). Photos were taken 14 d posttransfection.
• FIG. 45: A mixture of two short hairpins, both corresponding to firefly luciferase, does not result in a synergistic suppression of gene expression. Suppression of firefly luciferase gene expression resulting from transfection of a mixture of two different short hairpins ([0096]HP #1 and HP #2) was examined. The mixture ofHP #1 andHP #2 did not have a more robust effect on the suppression of firefly luciferase gene expression than expression ofHP #1 alone.
• FIG. 46: Encoded short hairpins specifically suppress gene expression in vivo. DNA oligonucleotides encoding 29 nucleotide hairpins corresponding to firefly luciferase were inserted into a vector containing the U6 promoter. Three independent constructs were examined for their ability to specifically suppress firefly luciferase gene expression in 293T cells. siOligo1-2, siOligo1-6, and siOligo1-19 (construct in the correct orientation) each suppressed gene expression as effectively as siRNA. In contrast, siOligo1-10 (construct in the incorrect orientation) did not suppress gene expression. An independent construct targeted to a different portion of the firefly luciferase gene did not effectively suppress gene expression in either orientation (siOligo2-23, siOligo2-36).[0097]
• FIGS.[0098]47-49: Strategies for stable expression of short dsRNAs.
• FIG. 50: Dual luciferase assays were performed as described in detail in FIGS.[0099]28-35, however the cells used in these experiments were PKR−/− murine embryonic fibroblasts (MEFs). Briefly, RNAi using long dsRNAs typically envokes a non-specific response in MEFs (due to PKR activity). To evaluate the effect of long dsRNA constructs to specifically inhibit gene expression in MEFs, RNAi was examined in PKR−/− MEFs. Such cells do not respond to dsRNA with a non-specific response. The data summarized in this figure demonstrates that in the absence of the non-specific PKR response, long dsRNA constructs specifically suppress gene expression in MEFs.
• FIG. 51: Is a schematic representation of the mouse tyrosinase promoter. Primers were used to amplify three separate regions in the proximal promoter, or to amplify sequence corresponding to an enhancer located approximately 12 kb upstream.[0100]
• FIG. 52: Reporter expression plasmids and siRNA sequences used in Figures X and Y. PGL-3-Control and Pluc-NS5B are the expression plasmids used for transfection into mouse liver. The nucleotide sequences of the siRNAs used in the study are shown underneath.[0101]
• FIG. 53: RNA interference in adult mice using siRNAs. (a) Representative images of light emitted from mice co-transfected with the luciferase plasmid pGL3-control and either no siRNA, luciferase siRNA or unrelated siRNA. A pseudocolour image representing intensity of emitted light (red, most intense; blue, least intense) superimposed on a greyscale reference image (for orientation) shows that RNAi functions in adult mice. Annealed 21-nucleotide siRNAs (40 μg; Dharmacon) were co-injected into the livers of mice with 2 μg pGL3-control DNA (Promega) and 800 units of RNasin (Promega) in 1.8 ml PBS buffer in 5-7 s. After 72 h, mice were anaesthetized and given 3 mg luciferin intraperitoneally 15 min before imaging. (b) siRNA results (six mice per group) from a representative experiment. Mice receiving luciferase siRNA emitted significantly less light than reporter-alone controls (one-way ANOVA with post hoc Fisher's test). Results for reporter alone and unrelated siRNA were statistically similar. Animals were treated according to the US National Institutes of Health's guidelines for animal care and the guidelines of Stanford University.[0102]
• FIG. 54: RNA interference in adult mice using shRNAs. (a) Representative images of light emitted from mice co-transfected with the luciferase plasmid control, pShh1-Ff1, and pShh1-Ff1rev. pShh1-Ff1, but not pShh1-Ff1rev, reduced luciferase expression in mice relative to the reporter-alone control. pShh1-Ff1 or pShh1-rev (10 μg) were co-injected with 2 μg pGL3-control in 1.8 ml PBS buffer. (b) Average of three independent shRNA experiments (n=5). Average values for the reporter-alone group are designated as 100% in each of the three experiments. Animals were treated according to the US National Institutes of Health's guidelines for animal care and the guidelines of Stanford University.[0103]
• FIG. 55: Heritable repression of Neil1 expression by RNAi in several tissues. (a) Expression of Neil1 mRNA in the livers of three mice containing the Neil1 shRNA transgene (shRNA-positive) or three siblings lacking the transgene (shRNA-negative) was assayed by RT-PCR (top row is Neil1). An RT-PCR of β-actin was done to ensure that equal quantities of mRNAs were tested for each mouse (second row). Expression of the neomycin resistance gene (neo), carried on the shRNA vector, was tested similarly (third row). Finally, the mice were genotyped using genomic DNA that was PCR-amplified with vector-specific primers (bottom row). (b) Similar studies were performed in the heart. (c) Similar studies were performed in the spleen. Animal procedures have been approved by the SUNY, Stony Brook Institutional Animal Care and Use Committee (IACUC).[0104]
• FIG. 56: Reduction in Neil1 protein correlates with the presence of siRNAs. (a) Expression of Neil1 protein was examined in protein extracts from the livers of mice carrying the shRNA transgene (shRNA-positive) or siblings lacking the transgene (shRNA-negative) by western blotting with Neil1-specific antiserum. A western blot for PCNA was used to standardize loading. (b) The presence of siRNAs in RNA derived from the livers of transgenic mice as assayed by northern blotting using a 300 nt probe, part of which was complementary to the shRNA sequence. We note siRNAs only in mice transgenic for the shRNA expression cassette.[0105]
DETAILED DESCRIPTION OF CERTAIN PREFERRED EMBODIMENTS
• I. Overview[0106]
• The present invention provides methods for attenuating gene expression in a cell using gene-targeted double stranded RNA (dsRNA). The dsRNA contains a nucleotide sequence that hybridizes under physiologic conditions of the cell to the nucleotide sequence of at least a portion of the gene to be inhibited (the “target” gene). The nucleotide sequence can hybridize to either coding or non-coding sequence of the target gene.[0107]
• A significant aspect to certain embodiments of the present invention relates to the demonstration in the present application that RNAi can in fact be accomplished both in cultured mammalian cells and in whole organisms. This had not been previously described in the art.[0108]
• Another salient feature of the present invention concerns the ability to carry out RNAi in higher eukaryotes, particularly in non-oocytic cells of mammals, e.g., cells from adult mammals as an example.[0109]
• Furthermore, in contrast to the teachings of the prior art, we demonstrate that RNAi in mammalian systems can be mediated with dsRNA identical or similar to non-coding sequence of a target gene. It was previously believed that although dsRNA identical or similar to non-coding sequences (i.e., promoter, enhancer, or intronic sequences) did not inhibit RNAi, such dsRNAs were not thought to mediate RNAi.[0110]
• As described in further detail below, the present invention(s) are based on the discovery that the RNAi phenomenum is mediated by a set of enzyme activities, including an essential RNA component, that are evolutionarily conserved in eukaryotes ranging from plants to mammals.[0111]
• One enzyme contains an essential RNA component. After partial purification, a multi-component nuclease (herein “RISC nuclease”) co-fractionates with a discrete, 22-nucleotide RNA species which may confer specificity to the nuclease through homology to the substrate mRNAs. The short RNA molecules are generated by a processing reaction from the longer input dsRNA. Without wishing to be bound by any particular theory, these 22mer guide RNAs may serve as guide sequences that instruct the RISC nuclease to destroy specific mRNAs corresponding to the dsRNA sequences.[0112]
• As illustrated, double stranded forms of the 22-mer guide RNA can be sufficient in length to induce sequence-dependent dsRNA inhibition of gene expression. In the illustrated example, dsRNA contructs are administered to cells having a recombinant luciferase reporter gene. In the control cell, e.g., no exogeneously added RNA, the level of expression of the luciferase reporter is normalized to be the value of “1”. As illustrated, both long (500-mer) and short (22-mer) dsRNA constructs complementary to the luciferase gene could inhibit expression of that gene product relative to the control cell. On the other hand, similarly sized dsRNA complementary to the coding sequence for another protein, green fluorescence protein (GFP), did not significantly effect the expression of luciferase—indicating that the inhibitory phenomena was in each case sequence-dependent. Likewise, single stranded 22-mers of luciferase did not inhibit expression of that gene—indicating that the inhibitory phenomena is double stranded-dependent.[0113]
• The appended examples also identify an enzyme, Dicer, that can produce the putative guide RNAs. Dicer is a member of the RNAse III family of nucleases that specifically cleave dsRNA and is evolutionarily conserved in worms, flies, plants, fungi and, as described herein, mammals. The enzyme has a distinctive structure which includes a helicase domain and dual RNAse III motifs. Dicer also contains a region of homology to the RDE1/QDE2/ARGONAUTE family, which have been genetically linked to RNAi in lower eukaryotes. Indeed, activation of, or overexpression of Dicer may be sufficient in many cases to permit RNA interference in otherwise non-receptive cells, such as cultured eukaryotic cells, or mammalian (non-oocytic) cells in culture or in whole organisms.[0114]
• In certain embodiments, the cells can be treated with an agent(s) that inhibits the general double-stranded RNA response(s) by the host cells, such as may give rise to sequence-independent apoptosis. For instance, the cells can be treated with agents that inhibit the dsRNA-dependent protein kinase known as PKR (protein kinase RNA-activated). Double stranded RNAs in mammalian cells typically activate protein kinase PKR and lead to apoptosis. The mechanism of action of PKR includes phosphorylation and inactivation of eIF2α (Fire (1999)[0115]Trends Genet15: 358). It has also been reported that induction of NF-κB by PKR is involved in apoptosis commitment and this process is mediated through activation of the IKK complex. This sequence-independent response may reflect a form of primitive immune response, since the presence of dsRNA is a common feature of many viral lifecycles.
• As described herein, Applicants have demonstrated that the PKR response can be overcome in favor of the sequence-specific RNAi response. However, in certain instances, it may be desirable to treat the cells with agents which inhibit expression of PKR, cause its destruction, and/or inhibit the kinase activity of PKR, and such methods are specifically contemplated for use in the present invention. Likewise, overexpression of agents which ectopically activate eIF2α can be used. Other agents which can be used to suppress the PKR response include inhibitors of IκB phosphorylation of IκB, inhibitors of IκB ubiquitination, inhibitors of IκB degradation, inhibitors of NF-κB nuclear translocation, and inhibitors of NF-κB interaction with κB response elements.[0116]
• Other inhibitors of sequence-independent dsRNA response in cells include the gene product of the vaccinia virus E3L. The E3L gene product contains two distinct domains. A conserved carboxy-terminal domain has been shown to bind double-stranded RNA (dsRNA) and inhibit the antiviral dsRNA response by cells. Expression of at least that portion of the E3L gene in the host cell, or the use of polypeptide or peptidomimetics thereof, can be used to suppress the general dsRNA response. Caspase inhibitors sensitize cells to killing by double-stranded RNA. Accordingly, ectopic expression or activation of caspases in the host cell can be used to suppress the general dsRNA response.[0117]
• In other embodiments, the subject method is carried out in cells which have little or no general response to double stranded RNA, e.g., have no PKR-dependent dsRNA response, at least under the culture conditions. As illustrated in FIGS.[0118]28-32, CHO and P19 cells can be used without having to inhibit PKR or other general dsRNA responses.
• Thus, the present invention provides a process and compositions for inhibiting expression of a target gene in a cell, especially a mammalian cell. In certain embodiments, the process comprises introduction of RNA (the “dsRNA construct”) with partial or fully double-stranded character into the cell or into the extracellular environment. Inhibition is specific in that a nucleotide sequence from a portion of the target gene is chosen to produce the dsRNA construct. The dsRNA may be identical or similar to coding or non-coding sequence of the target gene. In preferred embodiments, the method utilizes a cell in which Dicer and/or Argonaute activities are recombinantly expressed or otherwise ectopically activated. This process can be (1) effective in attenuating gene expression, (2) specific to the targeted gene, and (3) general in allowing inhibition of many different types of target gene.[0119]
• II. Definitions[0120]
• For convenience, certain terms employed in the specification, examples, and appended claims are collected here.[0121]
• As used herein, the term “vector” refers to a nucleic acid molecule capable of transporting another nucleic acid to which it has been linked. One type of vector is a genomic integrated vector, or “integrated vector”, which can become integrated into the chromsomal DNA of the host cell. Another type of vector is an episomal vector, i.e., a nucleic acid capable of extra-chromosomal replication. Vectors capable of directing the expression of genes to which they are operatively linked are referred to herein as “expression vectors”. In the present specification, “plasmid” and “vector” are used interchangeably unless otherwise clear from the context.[0122]
• As used herein, the term “nucleic acid” refers to polynucleotides such as deoxyribonucleic acid (DNA), and, where appropriate, ribonucleic acid (RNA). The term should also be understood to include, as applicable to the embodiment being described, single-stranded (such as sense or antisense) and double-stranded polynucleotides.[0123]
• As used herein, the term “gene” or “recombinant gene” refers to a nucleic acid comprising an open reading frame encoding a polypeptide of the present invention, including both exon and (optionally) intron sequences. The nucleic acid may also optionally include non-coding sequences such as promoter or enhancer sequences. A “recombinant gene” refers to nucleic acid encoding such regulatory polypeptides, that may optionally include intron sequences that are derived from chromosomal DNA. The term “intron” refers to a DNA sequence present in a given gene that is not translated into protein and is generally found between exons.[0124]
• A “protein coding sequence” or a sequence that “encodes” a particular polypeptide or peptide, is a nucleic acid sequence that is transcribed (in the case of DNA) and is translated (in the case of mRNA) into a polypeptide in vitro or in vivo when placed under the control of appropriate regulatory sequences. The boundaries of the coding sequence are determined by a start codon at the 5′ (amino) terminus and a translation stop codon at the 3′ (carboxy) terminus. A coding sequence can include, but is not limited to, cDNA from procaryotic or eukaryotic mRNA, genomic DNA sequences from procaryotic or eukaryotic DNA, and even synthetic DNA sequences. A transcription termination sequence will usually be located 3′ to the coding sequence.[0125]
• Likewise, “encodes”, unless evident from its context, will be meant to include DNA sequences that encode a polypeptide, as the term is typically used, as well as DNA sequences that are transcribed into inhibitory antisense molecules.[0126]
• The term “loss-of-function”, as it refers to genes inhibited by the subject RNAi method, refers to a diminishment in the level of expression of a gene(s) in the presence of one or more dsRNA construct(s) when compared to the level in the absense of such dsRNA construct(s).[0127]
• The term “expression” with respect to a gene sequence refers to transcription of the gene and, as appropriate, translation of the resulting mRNA transcript to a protein. Thus, as will be clear from the context, expression of a protein coding sequence results from transcription and translation of the coding sequence.[0128]
• “Cells,” “host cells” or “recombinant host cells” are terms used interchangeably herein. It is understood that such terms refer not only to the particular subject cell but to the progeny or potential progeny of such a cell. Because certain modifications may occur in succeeding generations due to either mutation or environmental influences, such progeny may not, in fact, be identical to the parent cell, but are still included within the scope of the term as used herein.[0129]
• The term “cultured cells” refers to cells suspended in culture, e.g., dispersed in culture or in the form tissue. It does not, however, include oocytes or whole embryos (including blastocysts and the like) which may be provided in culture. In certain embodiments, the cultured cells are adults cells, e.g., non-embryonic.[0130]
• By “recombinant virus” is meant a virus that has been genetically altered, e.g., by the addition or insertion of a heterologous nucleic acid construct into the particle.[0131]
• As used herein, the terms “transduction” and “transfection” are art recognized and mean the introduction of a nucleic acid, e.g., an expression vector, into a recipient cell by nucleic acid-mediated gene transfer. “Transformation”, as used herein, refers to a process in which a cell's genotype is changed as a result of the cellular uptake of exogenous DNA or RNA, and, for example, the transformed cell expresses a dsRNA contruct.[0132]
• “Transient transfection” refers to cases where exogenous DNA does not integrate into the genome of a transfected cell, e.g., where episomal DNA is transcribed into mRNA and translated into protein.[0133]
• A cell has been “stably transfected” with a nucleic acid construct when the nucleic acid construct is capable of being inherited by daughter cells.[0134]
• As used herein, a “reporter gene construct” is a nucleic acid that includes a “reporter gene” operatively linked to at least one transcriptional regulatory sequence. Transcription of the reporter gene is controlled by these sequences to which they are linked. The activity of at least one or more of these control sequences can be directly or indirectly regulated by the target receptor protein. Exemplary transcriptional control sequences are promoter sequences. A reporter gene is meant to include a promoter-reporter gene construct that is heterologously expressed in a cell.[0135]
• As used herein, “transformed cells” refers to cells that have spontaneously converted to a state of unrestrained growth, i.e., they have acquired the ability to grow through an indefinite number of divisions in culture. Transformed cells may be characterized by such terms as neoplastic, anaplastic and/or hyperplastic, with respect to their loss of growth control. For purposes of this invention, the terms “transformed phenotype of malignant mammalian cells” and “transformed phenotype” are intended to encompass, but not be limited to, any of the following phenotypic traits associated with cellular transformation of mammalian cells: immortalization, morphological or growth transformation, and tumorigenicity, as detected by prolonged growth in cell culture, growth in semi-solid media, or tumorigenic growth in immuno-incompetent or syngeneic animals.[0136]
• As used herein, “proliferating” and “proliferation” refer to cells undergoing mitosis.[0137]
• As used herein, “immortalized cells” refers to cells that have been altered via chemical, genetic, and/or recombinant means such that the cells have the ability to grow through an indefinite number of divisions in culture.[0138]
• The “growth state” of a cell refers to the rate of proliferation of the cell and the state of differentiation of the cell.[0139]
• “MHC antigen”, as used herein, refers to a protein product of one or more MHC genes; the term includes fragments or analogs of products of MHC genes which can evoke an immune response in a recipient organism. Examples of MHC antigens include the products (and fragments or analogs thereof) of the human MHC genes, i.e., the HLA genes.[0140]
• The term “histocompatibility” refers to the similarity of tissue between different individuals. The level of histocompatibility describes how well matched the patient and donor are. The major histocompatibility determinants are the human leukocyte antigens (HLA). HLA typing is performed between the potential marrow donor and the potential transplant recipient to determine how close a HLA match the two are. The closer the match the less the donated marrow and the patient's body will react against each other.[0141]
• The term “human leukocyte antigens” or “HLA”, refers to proteins (antigens) found on the surface of white blood cells and other tissues that are used to match donor and patient. For instances, a patient and potential donor may have their white blood cells tested for such HLA antigens as, HLA-A, B and DR. Each individual has two sets of these antigens, one set inherited from each parent. For this reason, it is much more likely for a brother or sister to match the patient than an unrelated individual, and much more likely for persons of the same racial and ethnic backgrounds to match each other.[0142]
• III. Exemplary Embodiments of Isolation Method[0143]
• One aspect of the invention provides a method for potentiating RNAi by induction or ectopic activation of an RNAi enzyme in a cell (in vivo or in vitro) or cell-free mixtures. In preferred embodiments, the RNAi activity is activated or added to a mammalian cell, e.g., a human cell, which cell may be provided in vitro or as part of a whole organism. In other embodiments, the subject method is carried out using eukaryotic cells generally (except for oocytes) in culture. For instance, the Dicer enzyme may be activated by virtue of being recombinantly expressed or it may be activated by use of an agent which (i) induces expression of the endogenous gene, (ii) stabilizes the protein from degradation, and/or (iii) allosterically modifies the enzyme to increase its activity (by altering its Kcat, Km or both).[0144]
• A. Dicer and Argonaut Activities[0145]
• In certain embodiments, at least one of the activated RNAi enzymes is Dicer, or a homolog thereof. In certain preferred embodiments, the present method provides for ectopic activation of Dicer. As used herein, the term “Dicer” refers to a protein which (a) mediates an RNAi response and (b) has an amino acid sequence at least 50 percent identical, and more preferably at least 75, 85, 90 or 95 percent identical to SEQ ID No. 2 or 4, and/or which can be encoded by a nucleic acid which hybridizes under wash conditions of 2×SSC at 22° C., and more preferably 0.2×SSC at 65° C., to a nucleotide represented by SEQ ID No. 1 or 3. Accordingly, the method may comprise introducing a dsRNA contruct into a cell in which Dicer has been recombinantly expressed or otherwise ectopically activated.[0146]
• In certain embodiment, at least one of the activated RNAi enzymes is Argonaut, or a homolog thereof. In certain preferred embodiments, the present method provides for ectopic activation of Argonaut. As used herein, the term “Argonaut” refers to a protein which (a) mediates an RNAi response and (b) has an amino acid sequence at least 50 percent identical, and more preferably at least 75, 85, 90 or 95 percent identical to the amino acid sequence shown in FIG. 24. Accordingly, the method may comprise introducing a dsRNA contruct into a cell in which Argonaut has been recombinantly expressed or otherwise ectopically activated.[0147]
• This invention also provides expression vectors containing a nucleic acid encoding a Dicer or Argonaut polypeptide, operably linked to at least one transcriptional regulatory sequence. Operably linked is intended to mean that the nucleotide sequence is linked to a regulatory sequence in a manner which allows expression of the nucleotide sequence. Regulatory sequences are art-recognized and are selected to direct expression of the subject Dicer or Argonaut proteins. Accordingly, the term transcriptional regulatory sequence includes promoters, enhancers and other expression control elements. Such regulatory sequences are described in Goeddel; Gene Expression Technology: Methods in Enzymology 185, Academic Press, San Diego, Calif. (1990). For instance, any of a wide variety of expression control sequences, sequences that control the expression of a DNA sequence when operatively linked to it, may be used in these vectors to express DNA sequences encoding Dicer or Argonaut polypeptides of this invention. Such useful expression control sequences, include, for example, a viral LTR, such as the LTR of the Moloney murine leukemia virus, the early and late promoters of SV40, adenovirus or cytomegalovirus immediate early promoter, the lac system, the trp system, the TAC or TRC system, T7 promoter whose expression is directed by T7 RNA polymerase, the major operator and promoter regions of phage λ, the control regions for fd coat protein, the promoter for 3-phosphoglycerate kinase or other glycolytic enzymes, the promoters of acid phosphatase, e.g., Pho5, the promoters of the yeast α-mating factors, the polyhedron promoter of the baculovirus system and other sequences known to control the expression of genes of prokaryotic or eukaryotic cells or their viruses, and various combinations thereof. It should be understood that the design of the expression vector may depend on such factors as the choice of the host cell to be transformed and/or the type of protein desired to be expressed.[0148]
• Moreover, the vector's copy number, the ability to control that copy number and the expression of any other proteins encoded by the vector, such as antibiotic markers, should also be considered.[0149]
• The recombinant Dicer or Argonaut genes can be produced by ligating a nucleic acid encoding a Dicer or Argonaut polypeptide into a vector suitable for expression in either prokaryotic cells, eukaryotic cells, or both. Expression vectors for production of recombinant forms of the subject Dicer or Argonaut polypeptides include plasmids and other vectors. For instance, suitable vectors for the expression of a Dicer or Argonaut polypeptide include plasmids of the types: pBR322-derived plasmids, pEMBL-derived plasmids, pEX-derived plasmids, pBTac-derived plasmids and pUC-derived plasmids for expression in prokaryotic cells, such as[0150]E. coli.
• A number of vectors exist for the expression of recombinant proteins in yeast. For instance, YEP24, YIP5, YEP51, YEP52, pYES2, and YRP17 are cloning and expression vehicles useful in the introduction of genetic constructs into[0151]S. cerevisiae(see, for example, Broach et al. (1983) in Experimental Manipulation of Gene Expression, ed. M. Inouye Academic Press, p. 83, incorporated by reference herein). These vectors can replicate inE. colidue the presence of the pBR322 ori, and inS. cerevisiaedue to the replication determinant of theyeast 2 micron plasmid. In addition, drug resistance markers such as ampicillin can be used. In an illustrative embodiment, a Dicer or Argonaut polypeptide is produced recombinantly utilizing an expression vector generated by sub-cloning the coding sequence of a Dicer or Argonaut gene.
• The preferred mammalian expression vectors contain both prokaryotic sequences, to facilitate the propagation of the vector in bacteria, and one or more eukaryotic transcription units that are expressed in eukaryotic cells. The pcDNAI/amp, pcDNAI/neo, pRc/CMV, pSV2gpt, pSV2neo, pSV2-dhfr, pTk2, pRSVneo, pMSG, pSVT7, pko-neo and pHyg derived vectors are examples of mammalian expression vectors suitable for transfection of eukaryotic cells. Some of these vectors are modified with sequences from bacterial plasmids, such as pBR322, to facilitate replication and drug resistance selection in both prokaryotic and eukaryotic cells. Alternatively, derivatives of viruses such as the bovine papillomavirus (BPV-1), or Epstein-Barr virus (pHEBo, pREP-derived and p205) can be used for transient expression of proteins in eukaryotic cells. The various methods employed in the preparation of the plasmids and transformation of host organisms are well known in the art. For other suitable expression systems for both prokaryotic and eukaryotic cells, as well as general recombinant procedures, see Molecular Cloning A Laboratory Manual, 2nd Ed., ed. by Sambrook, Fritsch and Maniatis (Cold Spring Harbor Laboratory Press: 1989)[0152]Chapters 16 and 17.
• In yet another embodiment, the subject invention provides a “gene activation” construct which, by homologous recombination with a genomic DNA, alters the transcriptional regulatory sequences of an endogenous Dicer or Argonaut gene. For instance, the gene activation construct can replace the endogenous promoter of a Dicer or Argonaut gene with a heterologous promoter, e.g., one which causes constitutive expression of the Dicer or Argonaut gene or which causes inducible expression of the gene under conditions different from the normal expression pattern of Dicer or Argonaut. A variety of different formats for the gene activation constructs are available. See, for example, the Transkaryotic Therapies, Inc PCT publications WO93/09222, WO95/31560, WO96/29411, WO95/31560 and WO94/12650.[0153]
• In preferred embodiments, the nucleotide sequence used as the gene activation construct can be comprised of (1) DNA from some portion of the endogenous Dicer or Argonaut gene (exon sequence, intron sequence, promoter sequences, etc.) which direct recombination and (2) heterologous transcriptional regulatory sequence(s) which is to be operably linked to the coding sequence for the genomic Dicer or Argonaut gene upon recombination of the gene activation construct. For use in generating cultures of Dicer or Argonaut producing cells, the construct may further include a reporter gene to detect the presence of the knockout construct in the cell.[0154]
• The gene activation construct is inserted into a cell, and integrates with the genomic DNA of the cell in such a position so as to provide the heterologous regulatory sequences in operative association with the native Dicer or Argonaut gene. Such insertion occurs by homologous recombination, i.e., recombination regions of the activation construct that are homologous to the endogenous Dicer or Argonaut gene sequence hybridize to the genomic DNA and recombine with the genomic sequences so that the construct is incorporated into the corresponding position of the genomic DNA.[0155]
• The terms “recombination region” or “targeting sequence” refer to a segment (i.e., a portion) of a gene activation construct having a sequence that is substantially identical to or substantially complementary to a genomic gene sequence, e.g., including 5′ flanking sequences of the genomic gene, and can facilitate homologous recombination between the genomic sequence and the targeting transgene construct.[0156]
• As used herein, the term “replacement region” refers to a portion of a activation construct which becomes integrated into an endogenous chromosomal location following homologous recombination between a recombination region and a genomic sequence.[0157]
• The heterologous regulatory sequences, e.g., which are provided in the replacement region, can include one or more of a variety of elements, including: promoters (such as constitutive or inducible promoters), enhancers, negative regulatory elements, locus control regions, transcription factor binding sites, or combinations thereof.[0158]
• Promoters/enhancers which may be used to control the expression of the targeted gene in vivo include, but are not limited to, the cytomegalovirus (CMV) promoter/enhancer (Karasuyama et al. (1989)[0159]J. Exp. Med169: 13), the human β-actin promoter (Gunning et al. (1987)PNAS84: 4831-4835), the glucocorticoid-inducible promoter present in the mouse mammary tumor virus long terminal repeat (MMTV LTR) (Klessig et al. (1984)Mol. Cell Biol.4: 1354-1362), the long terminal repeat sequences of Moloney murine leukemia virus (MuLV LTR) (Weiss et al. (1985)RNA Tumor Viruses, Cold Spring Harbor Laboratory, Cold Spring Harbor, N.Y.), the SV40 early or late region promoter (Bemoist et al. (1981)Nature290: 304-310; Templeton et al. (1984)Mol. Cell Biol.4: 817; and Sprague et al. (1983)J. Virol.45: 773), the promoter contained in the 3′ long terminal repeat of Rous sarcoma virus (RSV) (Yamamoto et al. (1980)Cell22: 787-797), the herpes simplex virus (HSV) thymidine kinase promoter/enhancer (Wagner et al. (1981)PNAS82: 3567-71), and the herpes simplex virus LAT promoter (Wolfe et al. (1992)Nature Genetics1: 379-384).
• In still other embodiments, the replacement region merely deletes a negative transcriptional control element of the native gene, e.g., to activate expression, or ablates a positive control element, e.g., to inhibit expression of the targeted gene.[0160]
• B. Cell/Organism[0161]
• The cell with the target gene may be derived from or contained in any organism (e.g., plant, animal, protozoan, virus, bacterium, or fungus). The dsRNA construct may be synthesized either in vivo or in vitro. Endogenous RNA polymerase of the cell may mediate transcription in vivo, or cloned RNA polymerase can be used for transcription in vivo or in vitro. For generating double stranded transcripts from a transgene in vivo, a regulatory region may be used to transcribe the RNA strand (or strands). Furthermore, dsRNA can be generated by transcribing an RNA strand which forms a hairpin, thus producing a dsRNA.[0162]
• Genetic manipulation becomes possible in organisms that are not classical genetic models. Breeding and screening programs may be accelerated by the ability to rapidly assay the consequences of a specific, targeted gene disruption. Gene disruptions may be used to discover the function of the target gene, to produce disease models in which the target gene are involved in causing or preventing a pathological condition, and to produce organisms with improved economic properties.[0163]
• The cell with the target gene may be derived from or contained in any organism. The organism may be a plant, animal, protozoan, bacterium, virus, or fungus. The plant may be a monocot, dicot or gymnosperm; the animal may be a vertebrate or invertebrate. Preferred microbes are those used in agriculture or by industry, and those that are pathogenic for plants or animals. Fungi include organisms in both the mold and yeast morphologies.[0164]
• Plants include arabidopsis; field crops (e.g., alfalfa, barley, bean, corn, cotton, flax, pea, rape, rice, rye, safflower, sorghum, soybean, sunflower, tobacco, and wheat); vegetable crops (e.g., asparagus, beet, broccoli, cabbage, carrot, cauliflower, celery, cucumber, eggplant, lettuce, onion, pepper, potato, pumpkin, radish, spinach, squash, taro, tomato, and zucchini); fruit and nut crops (e.g., almond, apple, apricot, banana, blackberry, blueberry, cacao, cherry, coconut, cranberry, date, fajoa, filbert, grape, grapefruit, guava, kiwi, lemon, lime, mango, melon, nectarine, orange, papaya, passion fruit, peach, peanut, pear, pineapple, pistachio, plum, raspberry, strawberry, tangerine, walnut, and watermelon); and ornamentals (e.g., alder, ash, aspen, azalea, birch, boxwood, camellia, carnation, chrysanthemum, elm, fir, ivy, jasmine, juniper, oak, palm, poplar, pine, redwood, rhododendron, rose, and rubber).[0165]
• Examples of vertebrate animals include fish, mammal, cattle, goat, pig, sheep, rodent, hamster, mouse, rat, primate, and human.[0166]
• Invertebrate animals include nematodes, other worms, drosophila, and other insects. Representative generae of nematodes include those that infect animals (e.g., Ancylostoma, Ascaridia, Ascaris, Bunostomum, Caenorhabditis, Capillaria, Chabertia, Cooperia, Dictyocaulus, Haernonchus, Heterakis, Nematodirus, Oesophagostomum, Ostertagia, Oxyuris, Parascaris, Strongylus, Toxascaris, Trichuris, Trichostrongylus, Tflichonema, Toxocara, Uncinaria) and those that infect plants (e.g., Bursaphalenchus, Criconerriella, Diiylenchus, Ditylenchus, Globodera, Helicotylenchus, Heterodera, Longidorus, Melodoigyne, Nacobbus, Paratylenchus, Pratylenchus, Radopholus, Rotelynchus, Tylenchus, and Xiphinerna). Representative orders of insects include Coleoptera, Diptera, Lepidoptera, and Homoptera.[0167]
• The cell having the target gene may be from the germ line or somatic, totipotent or pluripotent, dividing or non-dividing, parenchyma or epithelium, immortalized or transformed, or the like. The cell may be a stem cell or a differentiated cell. Cell types that are differentiated include adipocytes, fibroblasts, myocytes, cardiomyocytes, endothelium, neurons, glia, blood cells, megakaryocytes, lymphocytes, macrophages, neutrophils, eosinophils, basophils, mast cells, leukocytes, granulocytes, keratinocytes, chondrocytes, osteoblasts, osteoclasts, hepatocytes, and cells of the endocrine or exocrine glands.[0168]
• C. Targeted Genes[0169]
• The target gene may be a gene derived from the cell, an endogenous gene, a transgene, or a gene of a pathogen which is present in the cell after infection thereof. Depending on the particular target gene and the dose of double stranded RNA material delivered, the procedure may provide partial or complete loss of function for the target gene. Lower doses of injected material and longer times after administration of dsRNA may result in inhibition in a smaller fraction of cells. Quantitation of gene expression in a cell may show similar amounts of inhibition at the level of accumulation of target mRNA or translation of target protein.[0170]
• “Inhibition of gene expression” refers to the absence (or observable decrease) in the level of protein and/or mRNA product from a target gene. “Specificity” refers to the ability to inhibit the target gene without manifest effects on other genes of the cell. The consequences of inhibition can be confirmed by examination of the outward properties of the cell or organism (as presented below in the examples) or by biochemical techniques such as RNA solution hybridization, nuclease protection, Northern hybridization, reverse transcription, gene expression monitoring with a microarray, antibody binding, enzyme linked immunosorbent assay (ELISA), Western blotting, radioimmunoassay (RIA), other immunoassays, and fluorescence activated cell analysis (FACS). For RNA-mediated inhibition in a cell line or whole organism, gene expression is conveniently assayed by use of a reporter or drug resistance gene whose protein product is easily assayed. Such reporter genes include acetohydroxyacid synthase (AHAS), alkaline phosphatase (AP), beta galactosidase (LacZ), beta glucoronidase (GUS), chloramphenicol acetyltransferase (CAT), green fluorescent protein (GFP), horseradish peroxidase (HRP), luciferase (Luc), nopaline synthase (NOS), octopine synthase (OCS), and derivatives thereof. Multiple selectable markers are available that confer resistance to ampicillin, bleomycin, chloramphenicol, gentamycin, hygromycin, kanamycin, lincomycin, methotrexate, phosphinothricin, puromycin, and tetracyclin.[0171]
• Depending on the assay, quantitation of the amount of gene expression allows one to determine a degree of inhibition which is greater than 10%, 33%, 50%, 90%, 95% or 99% as compared to a cell not treated according to the present invention. Lower doses of injected material and longer times after administration of dsRNA may result in inhibition in a smaller fraction of cells (e.g., at least 10%, 20%, 50%, 75%, 90%, or 95% of targeted cells). Quantitation of gene expression in a cell may show similar amounts of inhibition at the level of accumulation of target mRNA or translation of target protein. As an example, the efficiency of inhibition may be determined by assessing the amount of gene product in the cell: mRNA may be detected with a hybridization probe having a nucleotide sequence outside the region used for the inhibitory double-stranded RNA, or translated polypeptide may be detected with an antibody raised against the polypeptide sequence of that region.[0172]
• As disclosed herein, the present invention is not limited to any type of target gene or nucleotide sequence. But the following classes of possible target genes are listed for illustrative purposes: developmental genes (e.g., adhesion molecules, cyclin kinase inhibitors, Writ family members, Pax family members, Winged helix family members, Hox family members, cytokines/lymphokines and their receptors, growth/differentiation factors and their receptors, neurotransmitters and their receptors); oncogenes (e.g., ABLI, BCLI, BCL2, BCL6, CBFA2, CBL, CSFIR, ERBA, ERBB, EBRB2, ETSI, ETS1, ETV6, FGR, FOS, FYN, HCR, HRAS, JUN, KRAS, LCK, LYN, MDM2, MLL, MYB, MYC, MYCLI, MYCN, NRAS, PIM 1, PML, RET, SRC, TALI, TCL3, and YES); tumor suppressor genes (e.g., APC, BRCA 1, BRCA2, MADH4, MCC, NF 1, NF2, RB 1, TP53, and WTI); and enzymes (e.g., ACC synthases and oxidases, ACP desaturases and hydroxylases, ADP-glucose pyrophorylases, ATPases, alcohol dehydrogenases, amylases, amyloglucosidases, catalases, cellulases, chalcone synthases, chitinases, cyclooxygenases, decarboxylases, dextrinases, DNA and RNA polymerases, galactosidases, glucanases, glucose oxidases, granule-bound starch synthases, GTPases, helicases, hemicellulases, integrases, inulinases, invertases, isomerases, kinases, lactases, lipases, lipoxygenases, lysozymes, nopaline synthases, octopine synthases, pectinesterases, peroxidases, phosphatases, phospholipases, phosphorylases, phytases, plant growth regulator synthases, polygalacturonases, proteinases and peptidases, pullanases, recombinases, reverse transcriptases, RUBISCOs, topoisomerases, and xylanases).[0173]
• D. dsRNA Constructs[0174]
• The dsRNA construct may comprise one or more strands of polymerized ribonucleotide. It may include modifications to either the phosphate-sugar backbone or the nucleoside. For example, the phosphodiester linkages of natural RNA may be modified to include at least one of a nitrogen or sulfur heteroatom. Modifications in RNA structure may be tailored to allow specific genetic inhibition while avoiding a general panic response in some organisms which is generated by dsRNA. Likewise, bases may be modified to block the activity of adenosine deaminase. The dsRNA construct may be produced enzymatically or by partial/total organic synthesis, any modified ribonucleotide can be introduced by in vitro enzymatic or organic synthesis.[0175]
• The dsRNA construct may be directly introduced into the cell (i.e., intracellularly); or introduced extracellularly into a cavity, interstitial space, into the circulation of an organism, introduced orally, or may be introduced by bathing an organism in a solution containing RNA. Methods for oral introduction include direct mixing of RNA with food of the organism, as well as engineered approaches in which a species that is used as food is engineered to express an RNA, then fed to the organism to be affected. Physical methods of introducing nucleic acids include injection of an RNA solution directly into the cell or extracellular injection into the organism.[0176]
• The double-stranded structure may be formed by a single self-complementary RNA strand or two complementary RNA strands. RNA duplex formation may be initiated either inside or outside the cell. The RNA may be introduced in an amount which allows delivery of at least one copy per cell. Higher doses (e.g., at least 5, 10, 100, 500 or 1000 copies per cell) of double-stranded material may yield more effective inhibition; lower doses may also be useful for specific applications. Inhibition is sequence-specific in that nucleotide sequences corresponding to the duplex region of the RNA are targeted for genetic inhibition.[0177]
• dsRNA constructs containing a nucleotide sequences identical to a portion, of either coding or non-coding sequence, of the target gene are preferred for inhibition. RNA sequences with insertions, deletions, and single point mutations relative to the target sequence (ds RNA similar to the target gene) have also been found to be effective for inhibition. Thus, sequence identity may be optimized by sequence comparison and alignment algorithms known in the art (see Gribskov and Devereux, Sequence Analysis Primer, Stockton Press, 1991, and references cited therein) and calculating the percent difference between the nucleotide sequences by, for example, the Smith-Waterman algorithm as implemented in the BESTFIT software program using default parameters (e.g., University of Wisconsin Genetic Computing Group). Greater than 90% sequence identity, or even 100% sequence identity, between the inhibitory RNA and the portion of the target gene is preferred. Alternatively, the duplex region of the RNA may be defined functionally as a nucleotide sequence that is capable of hybridizing with a portion of the target gene transcript (e.g., 400 mM NaCl, 40 mM PIPES pH 6.4, 1 mM EDTA, 50° C. or 70° C. hybridization for 12-16 hours; followed by washing). In certain preferred embodiments, the length of the dsRNA is at least 20, 21 or 22 nucleotides in length, e.g., corresponding in size to RNA products produced by Dicer-dependent cleavage. In certain embodiments, the dsRNA construct is at least 25, 50, 100, 200, 300 or 400 bases. In certain embodiments, the dsRNA construct is 400-800 bases in length.[0178]
• 100% sequence identity between the RNA and the target gene is not required to practice the present invention. Thus the invention has the advantage of being able to tolerate sequence variations that might be expected due to genetic mutation, strain polymorphism, or evolutionary divergence.[0179]
• The dsRNA construct may be synthesized either in vivo or in vitro. Endogenous RNA polymerase of the cell may mediate transcription in vivo, or cloned RNA polymerase can be used for transcription in vivo or in vitro. For transcription from a transgene in vivo or an expression construct, a regulatory region (e.g., promoter, enhancer, silencer, splice donor and acceptor, polyadenylation) may be used to transcribe the dsRNA strand (or strands). Inhibition may be targeted by specific transcription in an organ, tissue, or cell type; stimulation of an environmental condition (e.g., infection, stress, temperature, chemical inducers); and/or engineering transcription at a developmental stage or age. The RNA strands may or may not be polyadenylated; the RNA strands may or may not be capable of being translated into a polypeptide by a cell's translational apparatus. The dsRNA construct may be chemically or enzymatically synthesized by manual or automated reactions. The dsRNA construct may be synthesized by a cellular RNA polymerase or a bacteriophage RNA polymerase (e.g., T3, T7, SP6). The use and production of an expression construct are known in the art (see also WO 97/32016; U.S. Pat. Nos. 5,593,874, 5,698,425, 5,712,135, 5,789,214, and 5,804,693; and the references cited therein). If synthesized chemically or by in vitro enzymatic synthesis, the RNA may be purified prior to introduction into the cell. For example, RNA can be purified from a mixture by extraction with a solvent or resin, precipitation, electrophoresis, chromatography or a combination thereof. Alternatively, the dsRNA construct may be used with no or a minimum of purification to avoid losses due to sample processing. The dsRNA construct may be dried for storage or dissolved in an aqueous solution. The solution may contain buffers or salts to promote annealing, and/or stabilization of the duplex strands.[0180]
• Physical methods of introducing nucleic acids include injection of a solution containing the dsRNA construct, bombardment by particles covered by the dsRNA construct, soaking the cell or organism in a solution of the RNA, or electroporation of cell membranes in the presence of the dsRNA construct. A viral construct packaged into a viral particle would accomplish both efficient introduction of an expression construct into the cell and transcription of dsRNA construct encoded by the expression construct. Other methods known in the art for introducing nucleic acids to cells may be used, such as lipid-mediated carrier transport, chemical mediated transport, such as calcium phosphate, and the like. Thus the dsRNA construct may be introduced along with components that perform one or more of the following activities: enhance RNA uptake by the cell, promote annealing of the duplex strands, stabilize the annealed strands, or other-wise increase inhibition of the target gene.[0181]
• E. Illustrative Uses[0182]
• One utility of the present invention is as a method of identifying gene function in an organism, especially higher eukaryotes, comprising the use of double-stranded RNA to inhibit the activity of a target gene of previously unknown function. Instead of the time consuming and laborious isolation of mutants by traditional genetic screening, functional genomics would envision determining the function of uncharacterized genes by employing the invention to reduce the amount and/or alter the timing of target gene activity. The invention could be used in determining potential targets for pharmaceuticals, understanding normal and pathological events associated with development, determining signaling pathways responsible for postnatal development/aging, and the like. The increasing speed of acquiring nucleotide sequence information from genomic and expressed gene sources, including total sequences for mammalian genomes, can be coupled with the invention to determine gene function in a cell or in a whole organism. The preference of different organisms to use particular codons, searching sequence databases for related gene products, correlating the linkage map of genetic traits with the physical map from which the nucleotide sequences are derived, and artificial intelligence methods may be used to define putative open reading frames from the nucleotide sequences acquired in such sequencing projects.[0183]
• A simple assay would be to inhibit gene expression according to the partial sequence available from an expressed sequence tag (EST). Functional alterations in growth, development, metabolism, disease resistance, or other biological processes would be indicative of the normal role of the EST's gene product.[0184]
• The ease with which the dsRNA construct can be introduced into an intact cell/organism containing the target gene allows the present invention to be used in high throughput screening (HTS). For example, duplex RNA can be produced by an amplification reaction using primers flanking the inserts of any gene library derived from the target cell or organism. Inserts may be derived from genomic DNA or mRNA (e.g., cDNA and cRNA). Individual clones from the library can be replicated and then isolated in separate reactions, but preferably the library is maintained in individual reaction vessels (e.g., a 96 well microtiter plate) to minimize the number of steps required to practice the invention and to allow automation of the process.[0185]
• In an exemplary embodiment, the subject invention provides an arrayed library of RNAi constructs. The array may be in the form of solutions, such as multi-well plates, or may be “printed” on solid substrates upon which cells can be grown. To illustrate, solutions containing duplex RNAs that are capable of inhibiting the different expressed genes can be placed into individual wells positioned on a microtiter plate as an ordered array, and intact cells/organisms in each well can be assayed for any changes or modifications in behavior or development due to inhibition of target gene activity.[0186]
• In one embodiment, the subject method uses an arrayed library of RNAi constructs to screen for combinations of RNAi that are lethal to host cells. Synthetic lethality is a bedrock principle of experimental genetics. A synthetic lethality describes the properties of two mutations which, individually, are tolerated by the organism but which, in combination, are lethal. The subject arrays can be used to identify loss-of-function mutations that are lethal in combination with alterations in other genes, such as activated oncogenes or loss-of-function mutations to tumor suppressors. To achieve this, one can create “phenotype arrays” using cultured cells. Expression of each of a set of genes, such as the host cell's genome, can be individually systematically disrupted using RNA interference. Combination with alterations in oncogene and tumor suppressor pathways can be used to identify synthetic lethal interactions that may identify novel therapeutic targets.[0187]
• In certain embodiments, the RNAi constructs can be fed directly to, or injected into, the cell/organism containing the target gene. Alternatively, the duplex RNA can be produced by in vivo or in vitro transcription from an expression construct used to produce the library. The construct can be replicated as individual clones of the library and transcribed to produce the RNA; each clone can then be fed to, injected into, or delivered by another method known in the art to the cell/organism containing the target gene. The function of the target gene can be assayed from the effects it has on the cell/organism when gene activity is inhibited. This screening could be amenable to small subjects that can be processed in large number, for example, tissue culture cells derived from mammals, especially primates, and most preferably humans.[0188]
• If a characteristic of an organism is determined to be genetically linked to a polymorphism through RFLP or QTL analysis, the present invention can be used to gain insight regarding whether that genetic polymorphism might be directly responsible for the characteristic. For example, a fragment defining the genetic polymorphism or sequences in the vicinity of such a genetic polymorphism can be amplified to produce an RNA, the duplex RNA can be introduced to the organism or cell, and whether an alteration in the characteristic is correlated with inhibition can be determined. Of course, there may be trivial explanations for negative results with this type of assay, for example: inhibition of the target gene causes lethality, inhibition of the target gene may not result in any observable alteration, the fragment contains nucleotide sequences that are not capable of inhibiting the target gene, or the target gene's activity is redundant.[0189]
• The present invention may be useful in allowing the inhibition of essential genes. Such genes may be required for cell or organism viability at only particular stages of development or only in specific cellular compartments or tissues. The functional equivalent of conditional mutations may be produced by inhibiting activity of the target gene when or where it is not required for viability. The invention allows addition of RNA at specific times of development and locations in the organism without introducing permanent mutations into the target genome.[0190]
• The present invention may be useful in allowing the inhibition of genes that have been difficult to inhibit using other methods due to gene redundancy. Since the present methods may be used to deliver more than one dsRNA to a cell or organism, dsRNA identical or similar to more than one gene, wherein the genes have a redundant function during normal development, may be delivered.[0191]
• If alternative splicing produced a family of transcripts that were distinguished by usage of characteristic exons, the present invention can target inhibition through the appropriate exons to specifically inhibit or to distinguish among the functions of family members. For example, a protein factor that contained an alternatively spliced transmembrane domain may be expressed in both membrane bound and secreted forms. Instead of isolating a nonsense mutation that terminates translation before the transmembrane domain, the functional consequences of having only secreted hormone can be determined according to the invention by targeting the exon containing the transmembrane domain and thereby inhibiting expression of membrane-bound hormone. That is, the subject method can be used for selected ablation of splicing variants.[0192]
• The present invention may be used alone or as a component of a kit having at least one of the reagents necessary to carry out the in vitro or in vivo introduction of RNA to test samples or subjects. Preferred components are the dsRNA and a vehicle that promotes introduction of the dsRNA. Such a kit may also include instructions to allow a user of the kit to practice the invention.[0193]
• Alternatively, an organism may be engineered to produce dsRNA which produces commercially or medically beneficial results, for example, resistance to a pathogen or its pathogenic effects, improved growth, or novel developmental patterns.[0194]
IV. Exemplification
• The invention, now being generally described, will be more readily understood by reference to the following examples, which are included merely for purposes of illustration of certain aspects and embodiments of the present invention and are not intended to limit the invention.[0195]
EXAMPLE 1An RNA-Directed Nuclease Mediates RNAi Gene Silencing
• In a diverse group of organisms that includes[0196]Caenorhabditis elegans, Drosophila, planaria, hydra, trypanosomes, fungi and plants, the introduction of double-stranded RNAs inhibits gene expression in a sequence-specific manner (Sharp (1999)Genes and Development13: 139-141; Sanchez-Alvarado and Newmark (1999)PNAS96: 5049-5054; Lohman et al. (1999)Developmental Biology214: 211-214; Cogoni and Macino (1999)Nature399: 166-169; Waterhouse et al. (1998)PNAS95: 13959-13964; Montgomery and Fire (1998)Trends Genet.14: 225-228; Ngo et al. (1998)PNAS95: 14687-14692). These responses, called RNA interference or post-transcriptional gene silencing, may provide anti-viral defence, modulate transposition or regulate gene expression (Sharp (1999)Genes and Development13: 139-141; Montgomery and Fire (1998)Trends Genet.14: 225-228; Tabara et al. (1999)Cell99: 123-132; Ketting et al. (1999)Cell99: 133-141; Ratcliff et al. (1997)Science276: 1558-1560). We have taken a biochemical approach towards elucidating the mechanisms underlying this genetic phenomenon. Here we show that ‘loss-of-function’ phenotypes can be created in cultured Drosophila cells by transfection with specific double-stranded RNAs. This coincides with a marked reduction in the level of cognate cellular messenger RNAs. Extracts of transfected cells contain a nuclease activity that specifically degrades exogenous transcripts homologous to transfected double-stranded RNA. This enzyme contains an essential RNA component. After partial purification, the sequence-specific nuclease co-fractionates with a discrete, ˜25-nucleotide RNA species which may confer specificity to the enzyme through homology to the substrate mRNAs.
• Although double-stranded RNAs (dsRNAs) can provoke gene silencing in numerous biological contexts including Drosophila (Kennerdell et al. (1998)[0197]Cell95: 1017-1026; Misquitta and Paterson (1999)PNAS96: 1451-1456), the mechanisms underlying this phenomenon have remained mostly unknown. We therefore wanted to establish a biochemically tractable model in which such mechanisms could be investigated.
• Transient transfection of cultured, Drosophila S2 cells with a lacZ expression vector resulted in β-galactosidase activity that was easily detectable by an in situ assay (FIG. 1[0198]a). This activity was greatly reduced by co-transfection with a dsRNA corresponding to the first 300 nucleotides of the lacZ sequence, whereas co-transfection with a control dsRNA (CD8) (FIG. 1a) or with single-stranded RNAs of either sense or antisense orientation (data not shown) had little or no effect. This indicated that dsRNAs could interfere, in a sequence-specific fashion, with gene expression in cultured cells.
• To determine whether RNA interference (RNAi) could be used to target endogenous genes, we transfected S2 cells with a dsRNA corresponding to the first 540 nucleotides of Drosophila cyclin E, a gene that is essential for progression into S phase of the cell cycle. During log-phase growth, untreated S2 cells reside primarily in G2/M (FIG. 1[0199]b). Transfection with lacZ dsRNA had no effect on cell-cycle distribution, but transfection with the cyclin E dsRNA caused a G1-phase cell-cycle arrest (FIG. 1b). The ability of cyclin E dsRNA to provoke this response was length-dependent. Double-stranded RNAs of 540 and 400 nucleotides were quite effective, whereas dsRNAs of 200 and 300 nucleotides were less potent. Double-stranded cyclin E RNAs of 50 or 100 nucleotides were inert in our assay, and transfection with a single-stranded, antisense cyclin E RNA had virtually no effect.
• One hallmark of RNAi is a reduction in the level of mRNAs that are homologous to the dsRNA. Cells transfected with the cyclin E dsRNA (bulk population) showed diminished endogenous cyclin E mRNA as compared with control cells (FIG. 1[0200]c). Similarly, transfection of cells with dsRNAs homologous to fizzy, a component of the anaphase-promoting complex (APC) or cyclin A, a cyclin that acts in S, G2 and M, also caused reduction of their cognate mRNAs (FIG. 1c). The modest reduction in fizzy mRNA levels in cells transfected with cyclin A dsRNA probably resulted from arrest at a point in the division cycle at which fizzy transcription is low (Wolf and Jackson (1998)Current Biology8: R637-R639; Kramer et al. (1998)Current Biology8: 1207-1210). These results indicate that RNAi may be a generally applicable method for probing gene function in cultured Drosophila cells.
• The decrease in mRNA levels observed upon transfection of specific dsRNAs into Drosophila cells could be explained by effects at transcriptional or post-transcriptional levels. Data from other systems have indicated that some elements of the dsRNA response may affect mRNA directly (reviewed in Sharp (1999)[0201]Genes and Development13: 139-141; Montgomery and Fire (1998)Trends Genet.14: 225-228). We therefore sought to develop a cell-free assay that reflected, at least in part, RNAi.
• S2 cells were transfected with dsRNAs corresponding to either cyclin E or lacZ. Cellular extracts were incubated with synthetic mRNAs of lacZ or cyclin E. Extracts prepared from cells transfected with the 540-nucleotide cyclin E dsRNA efficiently degraded the cyclin E transcript; however, the lacZ transcript was stable in these lysates (FIG. 2[0202]a). Conversely, lysates from cells transfected with the lacZ dsRNA degraded the lacZ transcript but left the cyclin E mRNA intact. These results indicate that RNAi ablates target mRNAs through the generation of a sequence-specific nuclease activity. We have termed this enzyme RISC (RNA-induced silencing complex). Although we occasionally observed possible intermediates in the degradation process (see FIG. 2), the absence of stable cleavage end-products indicates an exonuclease (perhaps coupled to an endonuclease). However, it is possible that the RNAi nuclease makes an initial endonucleolytic cut and that non-specific exonucleases in the extract complete the degradation process (Shuttleworth and Colman (1988)EMBO J.7: 427-434). In addition, our ability to create an extract that targets lacZ in vitro indicates that the presence of an endogenous gene is not required for the RNAi response.
• To examine the substrate requirements for the dsRNA-induced, sequence-specific nuclease activity, we incubated a variety of cyclin-E-derived transcripts with an extract derived from cells that had been transfected with the 540-nucleotide cyclin E dsRNA (FIG. 2[0203]b, c). Just as a length requirement was observed for the transfected dsRNA, the RNAi nuclease activity showed a dependence on the size of the RNA substrate. Both a 600-nucleotide transcript that extends slightly beyond the targeted region (FIG. 2b) and an ˜1-kilobase (kb) transcript that contains the entire coding sequence (data not shown) were completely destroyed by the extract. Surprisingly, shorter substrates were not degraded as efficiently. Reduced activity was observed against either a 300- or a 220-nucleotide transcript, and a ˜100-nucleotide transcript was resistant to nuclease in our assay. This was not due solely to position effects because ˜100-nucleotide transcripts derived from other portions of the transfected dsRNA behaved similarly (data not shown). As expected, the nuclease activity (or activities) present in the extract could also recognize the antisense strand of the cyclin E mRNA. Again, substrates that contained a substantial portion of the targeted region were degraded efficiently whereas those that contained a shorter stretch of homologous sequence (˜130 nucleotides) were recognized inefficiently (FIG. 2c, as600). For both the sense and antisense strands, transcripts that had no homology with the transfected dsRNA (FIG. 2b, Eout; FIG. 2c, as300) were not degraded. Although we cannot exclude the possibility that nuclease specificity could have migrated beyond the targeted region, the resistance of transcripts that do not contain homology to the dsRNA is consistent with data fromC. elegans. Double-stranded RNAs homologous to an upstream cistron have little or no effect on a linked downstream cistron, despite the fact that unprocessed, polycistronic mRNAs can be readily detected (Tabara et al. (1998)Science282: 430-432; Bosher et al. (1999)Genetics153: 1245-1256). Furthermore, the nuclease was inactive against a dsRNA identical to that used to provoke the RNAi response in vivo (FIG. 2b). In the in vitro system, neither a 5′ cap nor a poly(A) tail was required, as such transcripts were degraded as efficiently as uncapped and non-polyadenylated RNAs.
• Gene silencing provoked by dsRNA is sequence specific. A plausible mechanism for determining specificity would be incorporation of nucleic-acid guide sequences into the complexes that accomplish silencing (Hamilton and Baulcombe (1999)[0204]Science286: 950-952). In accord with this idea, pre-treatment of extracts with a Ca²⁺-dependent nuclease (micrococcal nuclease) abolished the ability of these extracts to degrade cognate mRNAs (FIG. 3). Activity could not be rescued by addition of non-specific RNAs such as yeast transfer RNA. Although micrococcal nuclease can degrade both DNA and RNA, treatment of the extract with DNAse I had no effect (FIG. 3). Sequence-specific nuclease activity, however, did require protein (data not shown). Together, our results support the possibility that the RNAi nuclease is a ribonucleoprotein, requiring both RNA and protein components. Biochemical fractionation (see below) is consistent with these components being associated in extract rather than being assembled on the target mRNA after its addition.
• In plants, the phenomenon of co-suppression has been associated with the existence of small (˜25-nucleotide) RNAs that correspond to the gene that is being silenced (Hamilton and Baulcombe (1999)[0205]Science286: 950-952). To address the possibility that a similar RNA might exist in Drosophila and guide the sequence-specific nuclease in the choice of substrate, we partially purified our activity through several fractionation steps. Crude extracts contained both sequence-specific nuclease activity and abundant, heterogeneous RNAs homologous to the transfected dsRNA (FIGS. 2 and 4a). The RNAi nuclease fractionated with ribosomes in a high-speed centrifugation step. Activity could be extracted by treatment with high salt, and ribosomes could be removed by an additional centrifugation step. Chromatography of soluble nuclease over an anion-exchange column resulted in a discrete peak of activity (FIG. 4b, cyclin E). This retained specificity as it was inactive against a heterologous mRNA (FIG. 4b, lacZ). Active fractions also contained an RNA species of 25 nucleotides that is homologous to the cyclin E target (FIG. 4b, northern). The band observed on northern blots may represent a family of discrete RNAs because it could be detected with probes specific for both the sense and antisense cyclin E sequences and with probes derived from distinct segments of the dsRNA (data not shown). At present, we cannot determine whether the 25-nucleotide RNA is present in the nuclease complex in a double-stranded or single-stranded form.
• RNA interference allows an adaptive defence against both exogenous and endogenous dsRNAs, providing something akin to a dsRNA immune response. Our data, and that of others (Hamilton and Baulcombe (1999)[0206]Science286: 950-952), is consistent with a model in which dsRNAs present in a cell are converted, either through processing or replication, into small specificity determinants of discrete size in a manner analogous to antigen processing. Our results suggest that the post-transcriptional component of dsRNA-dependent gene silencing is accomplished by a sequence-specific nuclease that incorporates these small RNAs as guides that target specific messages based upon sequence recognition. The identical size of putative specificity determinants in plants (Hamilton and Baulcombe (1999)Science286: 950-952) and animals predicts a conservation of both the mechanisms and the components of dsRNA-induced, post-transcriptional gene silencing in diverse organisms. In plants, dsRNAs provoke not only post-transcriptional gene silencing but also chromatin remodelling and transcriptional repression (Jones et al. (1998)EMBO J.17: 6385-6393; Jones et al. (1999)Plant Cell11: 2291-2301). It is now critical to determine whether conservation of gene-silencing mechanisms also exists at the transcriptional level and whether chromatin remodelling can be directed in a sequence-specific fashion by these same dsRNA-derived guide sequences.
• Methods:[0207]
• Cell culture and RNA methods S2 cells (Schneider (1972)[0208]J. Embryol Exp Morpho27: 353-365) were cultured at 27° C. in 90% Schneider's insect media (Sigma), 10% heat inactivated fetal bovine serum (FBS). Cells were transfected with dsRNA and plasmid DNA by calcium phosphate co-precipitation (DiNocera and Dawid (1983)PNAS80: 7095-7098). Identical results were observed when cells were transfected using lipid reagents (for example, Superfect, Qiagen). For FACS analysis, cells were additionally transfected with a vector that directs expression of a green fluorescent protein (GFP)-US9 fusion protein (Kalejta et al. (1999)Exp Cell Res.248: 322-328). These cells were fixed in 90% ice-cold ethanol and stained with propidium iodide at 25 μg/ml. FACS was performed on an Elite flow cytometer (Coulter). For northern blotting, equal loading was ensured by over-probing blots with a control complementary DNA (RP49). For the production of dsRNA, transcription templates were generated by polymerase chain reaction such that they contained T7 promoter sequences on each end of the template. RNA was prepared using the RiboMax kit (Promega). Confirmation that RNAs were double stranded came from their complete sensitivity to RNAse III (a gift from A. Nicholson). Target mRNA transcripts were synthesized using the Riboprobe kit (Promega) and were gel purified before use.
• Extract preparation Log-phase S2 cells were plated on 15-cm tissue culture dishes and transfected with 30 μg dsRNA and 30 μg carrier plasmid DNA. Seventy-two hours after transfection, cells were harvested in PBS containing 5 mM EGTA, washed twice in PBS and once in hypotonic buffer (10 mM HEPES pH 7.3, 6 mM β-mercaptoethanol). Cells were suspended in 0.7 packed-cell volumes of hypotonic buffer containing Complete protease inhibitors (Boehringer) and 0.5 units/ml of RNasin (Promega). Cells were disrupted in a dounce homogenizer with a type B pestle, and lysates were centrifuged at 30,000 g for 20 min. Supernatants were used in an in vitro assay containing 20 mM HEPES pH 7.3, 110 mM KOAc, 1 mM Mg(OAc)[0209]₂, 3 mM EGTA, 2 mM CaCl₂, 1 mM DTT. Typically, 5 μl extract was used in a 10 μl assay that contained also 10,000 c.p.m. synthetic mRNA substrate.
• Extract fractionation Extracts were centrifuged at 200,000 g for 3 h and the resulting pellet (containing ribosomes) was extracted in hypotonic buffer containing also 1 mM MgCl[0210]₂and 300 mM KOAc. The extracted material was spun at 100,000 g for 1 h and the resulting supernatant was fractionated on Source 15Q column (Pharmacia) using a KCl gradient in buffer A (20 mM HEPES pH 7.0, 1 mM dithiothreitol, 1 mM MgCl₂). Fractions were assayed for nuclease activity as described above. For northern blotting, fractions were proteinase K/SDS treated, phenol extracted, and resolved on 15% acrylamide 8M urea gels. RNA was electroblotted onto Hybond N+ and probed with strand-specific riboprobes derived from cyclin E mRNA. Hybridization was carried out in 500 mM NaPO₄pH 7.0, 15% formamide, 7% SDS, 1% BSA. Blots were washed in 1×SSC at 37-45° C.
EXAMPLE 2Role for a Bidentate Ribonuclease in the Initiation Step of RNA Interference
• Genetic approaches in worms, fungi and plants have identified a group of proteins that are essential for double-stranded RNA-induced gene silencing. Among these are ARGONAUTE family members (e.g. RDE1, QDE2) (Tabara et al. (1999)[0211]Cell99: 123-132; Catalanotto et al. (2000)Nature404: 245; Fagard et al. (2000)PNAS97: 11650-11654), recQ-family helicases (MUT-7, QDE3) (Ketting et al. (1999)Cell99: 133-141; Cogoni and Macino. (1999)Science286: 2342-2344), and RNA-dependent RNA polymerases (e.g. EGO-1, QDE1, SGS2/SDE1) (Cogoni and Macino (1999)Nature399: 166-169; Smardon et al. (2000)Current Biology10: 169-178; Mourrain et al. (2000)Cell101: 533-542; Dalmay et al. (2000)Cell101: 543-553). While potential roles have been proposed, none of these genes has been assigned a definitive function in the silencing process. Biochemical studies have suggested that PTGS is accomplished by a multicomponent nuclease that targets mRNAs for degradation (Hammond et al. (2000)Nature404: 293-296; Zamore et al. (2000)Cell101 25-33; Tuschl et al. (1999)Genes and Development13: 3191-3197). We have shown that the specificity of this complex may derive from the incorporation of a small guide sequence that is homologous to the mRNA substrate (Hammond et al. (2000)Nature404: 293-296). Originally identified in plants that were actively silencing transgenes (Hamilton and Baulcombe (1999)Science286: 950-952), these ˜22 nt. RNAs have been produced during RNAi in vitro using an extract prepared from Drosophila embryos (Zamore et al. (2000)Cell101 25-33). Putative guide RNAs can also be produced in extracts from Drosophila S2 cells (FIG. 5a). With the goal of understanding the mechanism of post-transcriptional gene silencing, we have undertaken both biochemical fractionation and candidate gene approaches to identify the enzymes that execute each step of RNAi.
• Our previous studies resulted in the partial purification of a nuclease, RISC, that is an effector of RNA interference. See Example 1. This enzyme was isolated from Drosophila S2 cells in which RNAi had been initiated in vivo by transfection with dsRNA. We first sought to determine whether the RISC enzyme and the enzyme that initiates RNAi via processing of dsRNA into 22mers are distinct activities. RISC activity could be largely cleared from extracts by high-speed centrifugation (100,000×g for 60 min.) while the activity that produces 22mers remained in the supernatant (FIG. 5[0212]b,c). This simple fractionation indicated that RISC and the 22mer-generating activity are separable and thus distinct enzymes. However, it seems likely that they might interact at some point during the silencing process.
• RNAse III family members are among the few nucleases that show specificity for double-stranded RNA (Nicholson (1999)[0213]FEMS Microbiol Rev23: 371-390). Analysis of the Drosophila andC. elegansgenomes reveals several types of RNAse III enzymes. First is the canonical RNAse III which contains a single RNAse III signature motif and a double-stranded RNA binding domain (dsRBD; e.g. RNC_CAEEL). Second is a class represented by Drosha (Filippov et al. (2000)Gene245: 213-221), a Drosophila enzyme that contains two RNAse III motifs and a dsRBD (CeDrosha inC. elegans). A third class contains two RNAse III signatures and an amino terminal helicase domain (e.g. Drosophila CG4792, CG6493,C. elegansK12H4.8), and these had previously been proposed by Bass as candidate RNAi nucleases (Bass (2000)Cell101: 235-238). Representatives of all three classes were tested for the ability to produce discrete, ˜22 nt. RNAs from dsRNA substrates.
• Partial digestion of a 500 nt. cyclin E dsRNA with purified, bacterial RNAse III produced a smear of products while nearly complete digestion produced a heterogeneous group of 11-17 nucleotide RNAs (not shown). In order to test the dual-RNAse III enzymes, we prepared T7 epitope-tagged versions of Drosha and CG4792. These were expressed in transfected S2 cells and isolated by immunoprecipitation using antibody-agarose conjugates. Treatment of the dsRNA with the CG4792 immunoprecipitate yielded ˜22 nt. fragments similar to those produced in either S2 or embryo extracts (FIG. 6[0214]a). Neither activity in extract nor activity in immunoprecipitates depended on the sequence of the RNA substrate since dsRNAs derived from several genes were processed equivalently (see Supplement 1). Negative results were obtained with Drosha and with immunoprecipitates of a DExH box helicase (Homeless (Gillespie et al. (1995)Genes and Development9: 2495-2508); see FIG. 6a,b). Western blotting confirmed that each of the tagged proteins was expressed and immunoprecipitated similarly (see Supplement 2). Thus, we conclude that CG4792 may carry out the initiation step of RNA interference by producing ˜22 nt. guide sequences from dsRNAs. Because of its ability to digest dsRNA into uniformly sized, small RNAs, we have named this enzyme Dicer (Dcr). Dicer mRNA is expressed in embryos, in S2 cells, and in adult flies, consistent with the presence of functional RNAi machinery in all of these contexts (see Supplement 3).
• The possibility that Dicer might be the nuclease responsible for the production of guide RNAs from dsRNAs prompted us to raise an antiserum directed against the carboxy-terminus of the Dicer protein (Dicer-1, CG4792). This antiserum could immunoprecipitate a nuclease activity from either Drosophila embryo extracts or from S2 cell lysates that produced ˜22 nt. RNAs from dsRNA substrates (FIG. 6C). The putative guide RNAs that are produced by the Dicer-1 enzyme precisely comigrate with 22mers that are produced in extract and with 22mers that are associated with the RISC enzyme (FIG. 6D,F). It had previously been shown that the enzyme that produced guide RNAs in Drosophila embryo extracts was ATP-dependent (Zamore et al. (2000)[0215]Cell101 25-33). Depletion of this cofactor resulted in an ˜6-fold lower rate of dsRNA cleavage and in the production of RNAs with a slightly lower mobility. Of interest was the fact that both Dicer-I immunoprecipitates and extracts from S2 cells require ATP for the production of 22mers (FIG. 6D). We do not observe the accumulation of lower mobility products in these cases, although we do routinely observe these in ATP-depleted embryo extracts. The requirement of this nuclease for ATP is a quite unusual property. We hypothesize that this requirement could indicate that the enzyme may act processively on the dsRNA, with the helicase domain harnessing the energy of ATP hydrolysis both for unwinding guide RNAs and for translocation along the substrate.
• Efficient induction of RNA interference in[0216]C. elegansand in Drosophila has several requirements. For example, the initiating RNA must be double-stranded, and it must be several hundred nucleotides in length. To determine whether these requirements are dictated by Dicer, we characterized the ability of extracts and of immunoprecipitated enzyme to digest various RNA substrates. Dicer was inactive against single stranded RNAs regardless of length (see Supplement 4). The enyzme could digest both 200 and 500 nucleotide dsRNAs but was significantly less active with shorter substrates (see Supplement 4). Double-stranded RNAs as short as 35 nucleotides could be cut by the enzyme, albeit very inefficiently (data not shown). In contrast,E. coliRNAse III could digest to completion dsRNAs of 35 or 22 nucleotides (not shown). This suggests that the substrate preferences of the Dicer enzyme may contribute to but not wholly determine the size dependence of RNAi.
• To determine whether the Dicer enzyme indeed played a role in RNAi in vivo, we sought to deplete Dicer activity from S2 cells and test the effect on dsRNA-induced gene silencing. Transfection of S2 cells with a mixture of dsRNAs homologous to the two Drosophila Dicer genes (CG4792 and CG6493) resulted in an ˜6-7 fold reduction of Dicer activity either in whole cell lysates or in Dicer-1 immunoprecipitates (FIG. 7A,B). Transfection with a control dsRNA (murine caspase 9) had no effect. Qualitatively similar results were seen if Dicer was examined by Northern blotting (not shown). Depletion of Dicer in this manner substantially compromised the ability of cells to silence subsequently an exogenous, GFP transgene by RNAi (FIG. 7C). These results indicate that Dicer is involved in RNAi in vivo. The lack of complete inhibition of silencing could result from an incomplete suppression of Dicer (which is itself required for RNAi) or could indicate that in vivo, guide RNAs can be produced by more than one mechanism (e.g. through the action of RNA-dependent RNA polymerases).[0217]
• Our results indicate that the process of RNA interference can be divided into at least two distinct steps. According to this model, initiation of PTGS would occur upon processing of a double-stranded RNA by Dicer into ˜22 nucleotide guide sequences, although we cannot formally exclude the possibility that another, Dicer-associated nuclease may participate in this process. These guide RNAs would be incorporated into a distinct nuclease complex (RISC) that targets single-stranded mRNAs for degradation. An implication of this model is that guide sequences are themselves derived directly from the dsRNA that triggers the response. In accord with this model, we have demonstrated that[0218]³²P-labeled, exogenous dsRNAs that have been introduced into S2 cells by transfection are incorporated into the RISC enzyme as 22 mers (FIG. 7E). However, we cannot exclude the possibility that RNA-dependent RNA polymerases might amplify 22mers once they have been generated or provide an alternative method for producing guide RNAs.
• The structure of the Dicer enzyme provokes speculation on the mechanism by which the enzyme might produce discretely sized fragments irrespective of the sequence of the dsRNA (see[0219]Supplement 1, FIG. 8a). It has been established that bacterial RNAse III acts on its substrate as a dimer (Nicholson (1999)FEMS Microbiol Rev23: 371-390; Robertson et al. (1968)J Biol Chem243: 82-91; Dunn (1976)J Biol Chem251: 3807-3814). Similarly, a dimer of Dicer enzymes may be required for cleavage of dsRNAs into ˜22 nt. pieces. According to one model, the cleavage interval would be determined by the physical arrangement of the two RNAse III domains within Dicer enzyme (FIG. 8a). A plausible alternative model would dictate that cleavage was directed at a single position by the two RIII domains in a single Dicer protein. The 22 nucleotide interval could be dictated by interaction of neighboring Dicer enzymes or by translocation along the mRNA substrate. The presence of an integral helicase domain suggests that the products of Dicer cleavage might be single-stranded 22 mers that are incorporated into the RISC enzyme as such.
• A notable feature of the Dicer family is its evolutionary conservation. Homologs are found in[0220]C. elegans(K12H4.8), Arabidopsis (e.g., CARPEL FACTORY (Jacobson et al. (1999)Development126: 5231-5243), T25K16.4, AC012328_—1), mammals (Helicase-MOI (Matsuda et al. (2000)Biochim Biophys Acta1490: 163-169) andS. pombe(YC9A_SCHPO) (FIG. 8b, seeSupplements 6,7 for sequence comparisons). In fact, the human Dicer family member is capable of generating ˜22 nt. RNAs from dsRNA substrates (Supplement 5) suggesting that these structurally similar proteins may all share similar biochemical functions. It has been demonstrated that exogenous dsRNAs can affect gene function in early mouse embryos (Wianny et al. (2000)Nature Cell Biology2: 70-75), and our results suggest that this regulation may be accomplished by an evolutionarily conserved RNAi machinery.
• In addition to RNAseIII and helicase motifs, searches of the PFAM database indicate that each Dicer family member also contains a ZAP domain (FIG. 8[0221]c) (Sonnhammer et al. (1997)Proteins28: 405-420). This sequence was defined based solely upon its conservation in the Zwille/ARGONAUTE/Piwi family that has been implicated in RNAi by mutations inC. elegans(Rde-1) and Neurospora (Qde-2) (Tabara et al. (1999)Cell99: 123-132; Catalanotto et al (2000)Nature404: 245). Although the function of this domain is unknown, it is intriguing that this region of homology is restricted to two gene families that participate in dsRNA-dependent silencing. Both the ARGONAUTE and Dicer families have also been implicated in common biological processes, namely the determination of stem-cell fates. A hypomorphic allele of carpel factory, a member of the Dicer family in Arabidopsis, is characterized by increased proliferation in floral meristems (Jacobsen et al. (1999)Development126 5231-5243). This phenotype and a number of other characteristic features are also shared by Arabidopsis ARGONAUTE (ago1-1) mutants (Bohmert et al. (1998)EMBO J17: 170-180; C. Kidner and R. Martiennsen, pers. comm.). These genetic analyses begin to provide evidence that RNAi may be more than a defensive response to unusual RNAs but may also play important roles in the regulation of endogenous genes.
• With the identification of Dicer as a catalyst of the initiation step of RNAi, we have begun to unravel the biochemical basis of this unusual mechanism of gene regulation. It will be of critical importance to determine whether the conserved family members from other organisms, particularly mammals, also play a role in dsRNA-mediated gene regulation.[0222]
• Methods:[0223]
• Plasmid constructs. A full-length cDNA encoding Drosha was obtained by PCR from an EST sequenced by the Berkeley Drosophila genome project. The Homeless clone was a gift from Gillespie and Berg (Univ. Washington). The T7 epitope-tag was added to the amino terminus of each by PCR, and the tagged cDNAs were cloned into pRIP, a retroviral vector designed specifically for expression in insect cells (E. Bernstein, unpublished). In this vector, expression is driven by the[0224]Orgyia pseudotsugataIE2 promoter (Invitrogen). Since no cDNA was available for CG4792/Dicer, a genomic clone was amplified from a bacmid (BACR23F10; obtained from the BACPAC Resource Center in the Dept. of Human Genetics at the Roswell Park Cancer Institute). Again, during amplification, a T7 epitope tag was added at the amino terminus of the coding sequence. The human Dicer gene was isolated from a cDNA library prepared from HaCaT cells (GJH, unpublished). A T7-tagged version of the complete coding sequence was cloned into pCDNA3 (Invitrogen) for expression in human cells (LinX-A).
• Cell culture and extract preparation. S2 and embryo culture. S2 cells were cultured at 27° C. in 5% CO[0225]₂in Schneider's insect media supplemented with 10% heat inactivated fetal bovine serum (Gemini) and 1% antibiotic-antimycotic solution (Gibco BRL). Cells were harvested for extract preparation at 10×10⁶cells/ml. The cells were washed 1× in PBS and were resuspended in a hypotonic buffer (10 mM Hepes pH 7.0, 2 mM MgCl₂, 6 mM PME) and dounced. Cell lysates were spun 20,000×g for 20 minutes. Extracts were stored at −80° C. Drosophila embryos were reared in fly cages by standard methodologies and were collected every 12 hours. The embryos were dechorionated in 50% chlorox bleach and washed thoroughly with distilled water. Lysis buffer (10 mM Hepes, 10 mM KCl, 1.5 mM MgCl₂, 0.5 mM EGTA, 10 mM β-glycerophosphate, 1 mM DTT, 0.2 mM PMSF) was added to the embryos, and extracts were prepared by homogenization in a tissue grinder. Lysates were spun for two hours at 200,000×g and were frozen at −80° C. LinX-A cells, a highly-transfectable derivative of human 293 cells, (Lin Xie and GJH, unpublished) were maintained in DMEM/10% FCS.
• Transfections and immunoprecipitations. S2 cells were transfected using a calcium phosphate procedure essentially as previously described (Hammond et al. (2000)[0226]Nature404: 293-296). Transfection rates were ˜90% as monitored in controls using an in situ β-galactosidase assay. LinX-A cells were also transfected by calcium phosphate co-precipitation. For immunoprecipitations, cells (˜5×10⁶per IP) were transfected with various clones and lysed three days later in IP buffer (125 mM KOAc, 1 mM MgOAc, 1 mM CaCl₂, 5 mM EGTA, 20 mM Hepes pH 7.0, 1 mM DTT, 1% NP-40 plus Complete protease inhibitors (Roche)). Lysates were spun for 10 minutes at 14,000×g and supernatants were added to T7 antibody-agarose beads (Novagen). Antibody binding proceeded for 4 hours at 4° C. Beads were centrifuged and washed in lysis buffer three times, and once in reaction buffer. The Dicer antiserum was raised in rabbits using a KLH-conjugated peptide corresponding to the C-terminal 8 amino acids of Drosophila Dicer-1 (CG4792).
• Cleavage reactions. RNA preparation. Templates to be transcribed into dsRNA were generated by PCR with forward and reverse primers, each containing a T7 promoter sequence. RNAs were produced using Riboprobe (Promega) kits and were uniformly labeling during the transcription reaction with[0227]³²P-UTP. Single-stranded RNAs were purified from 1% agarose gels. dsRNA cleavage. Five microliters of embryo or S2 extracts were incubated for one hour at 30° C. with dsRNA in a reaction containing 20 mM Hepes pH 7.0, 2 mM MgOAc, 2 mM DTT, 1 mM ATP and 5% Superasin (Ambion). Immunoprecipitates were treated similarly except that a minimal volume of reaction buffer (including ATP and Superasin) and dsRNA were added to beads that had been washed in reaction buffer (see above). For ATP depletion, Drosophila embryo extracts were incubated for 20 minutes at 30° C. with 2 mM glucose and 0.375 U of hexokinase (Roche) prior to the addition of dsRNA.
• Northern and Western analysis. Total RNA was prepared from Drosophila embryos (0-12 hour), from adult flies, and from S2 cells using Trizol (Lifetech). Messenger RNA was isolated by affinity selection using magnetic oligo-dT beads (Dynal). RNAs were electrophoresed on denaturing formaldehyde/agarose gels, blotted and probed with randomly primed DNAs corresponding to Dicer. For Western analysis, T7-tagged proteins were immunoprecipitated from whole cell lysates in IP buffer using anti-T7-antibody-agarose conjugates. Proteins were released from the beads by boiling in Laemmli buffer and were separated by electrophoresis on 8% SDS PAGE. Following transfer to nitrocellulose, proteins were visualized using an HRP-conjugated anti-T7 antibody (Novagen) and chemiluminescent detection (Supersignal, Pierce).[0228]
• RNAi of Dicer. Drosophila S2 cells were transfected either with a dsRNA corresponding to mouse caspase 9 or with a mixture of two dsRNAs corresponding to Drosophila Dicer-1 and Dicer-2 (CG4792 and CG6493). Two days after the initial transfection, cells were again transfected with a mixture containing a GFP expression plasmid and either luciferase dsRNA or GFP dsRNA as previously described (Hammond et al. (2000)[0229]Nature404: 293-296). Cells were assayed for Dicer activity or fluorescence three days after the second transfection. Quantification of fluorescent cells was done on a Coulter EPICS cell sorter after fixation. Control transfections indicated that Dicer activity was not affected by the introduction of caspase 9 dsRNA.
EXAMPLE 3A Simplified Method for the Creation of Hairpin Constructs for RNA Interference
• In numerous model organisms, double stranded RNAs have been shown to cause effective and specific suppression of gene function (Bosher and Labouesse (2000)[0230]NatureCell Biology 2: E31-E36). This response, termed RNA interference or post-transcriptional gene silencing, has evolved into a highly effective reverse genetic tool inC. elegans, Drosophila, plants and numerous other systems. In these cases, double-stranded RNAs can be introduced by injection, transfection or feeding; however, in all cases, the response is both transient and systemic. Recently, stable interference with gene expression has been achieved by expression of RNAs that form snap-back or hairpin structures (Fortier and Belote (2000)Genesis26: 240-244; Kennerdell and Carthew (2000)Nature Biotechnology18: 896-898; Lam and Thummel (2000)Current Biology10: 957-963; Shi et al. (2000)RNA6: 1069-1076; Smith et al. (2000)Nature407: 319-320; Tavemarakis et al. (2000)Nature Genetics24: 180-183). This has the potential not only to allow stable silencing of gene expression but also inducible silencing as has been observed in trypanosomes and adult Drosophila (Fortier and Belote (2000)Genesis26: 240-244; Lam and Thummel (2000)Current Biology10: 957-963; Shi et al. (2000)RNA6: 1069-1076). The utility of this approach is somewhat hampered by the difficulties that arise in the construction of bacterial plasmids containing the long inverted repeats that are necessary to provoke silencing. In a recent report, it was stated that more than 1,000 putative clones were screened to identify the desired construct (Tavemarakis et al. (2000)Nature Genetics24: 180-183).
• The presence of hairpin structures often induces plasmid rearrangement, in part due to the[0231]E. colisbc proteins that recognize and cleave cruciform DNA structures (Connelly et al. (1996)Genes Cell1: 285-291). We have developed a method for the construction of hairpins that does not require cloning of inverted repeats, per se. Instead, the fragment of the gene that is to be silenced is cloned as a direct repeat, and the inversion is accomplished by treatment with a site-specific recombinase, either in vitro (or potentially in vivo) (see FIG. 27). Following recombination, the inverted repeat structure is stable in a bacterial strain that lacks an intact SBC system (DL759). We have successfully used this strategy to construct numerous hairpin expression constructs that have been successfully used to provoke gene silencing in Drosophila cells.
• In the following examples, we use this method to express long dsRNAs in a variety of mammalian cell types. We show that such long dsRNAs mediate RNAi in a variety of cell types. Additionally, since the vector described in FIG. 27 contains a selectable marker, dsRNAs produced in this manner can be stably expressed in cells. Accordingly, this method allows not only the examination of transient effects of RNA suppression in a cell, but also the effects of stable and prolonged RNA suppression.[0232]
• Methods:[0233]
• Plasmids expressing hairpin RNAs were constructed by cloning the first 500 basepairs of the GFP coding region into the FLIP cassette of pRIP-FLIP as a direct repeat. The FLIP cassette contains two directional cloning sites, the second of which is flanked by LoxP sites. The Zeocin gene, present between the cloning sites, maintains selection and stability. To create an inverted repeat for hairpin production, the direct repeat clones were exposed to Cre recombinase (Stratagene) in vitro and, afterwards, transformed into DL759[0234]E. Coli. These bacteria permit the replication of DNA containing cruciform structures, which tend to form inverted repeats.
EXAMPLE 4Long dsRNAs Suppress Gene Expression in Mammalian Cells
• Previous experiments have demonstrated that dsRNA, produced using a variety of methods including via the construction of hairpins, can suppress gene expression in Drosophila cells. We now demonstrate that dsRNA can also suppress gene expression in mammalian cells in culture. Additionally, the power of RNAi as a genetic tool would be greatly enhanced by the ability to engineer stable silencing of gene expression. We therefore undertook an effort to identify mammalian cells in which long dsRNAs could be used as RNAi triggers in the hope that these same cell lines would provide a platform upon which to develop stable silencing strategies. We demonstrate that RNA suppression can be mediated by stably expressing a long hairpin in a mammalian cell line. The ability to engineer stable silencing of gene expression in cultured mammalian cells, in addition to the ability to transiently silence gene expression, has many important applications.[0235]
• A. RNAi in Pluripotent Murine P19 Cells.[0236]
• We first sought to determine whether long dsRNA triggers could induce sequence-specific silencing in cultured murine cells, both to develop this approach as a tool for probing gene function and to allow mechanistic studies of dsRNA-induced silencing to be propagated to mammalian systems. We, therefore, attempted to extend previous studies in mouse embryos (Wianny et al. 2000, Nat. Cell Biol. 2: 70-75; Svoboda et al. 2000, Development 127: 4147-4156) by searching for RNAi-like mechanisms in pluripotent, embryonic cell types. We surveyed a number of cell lines of embryonic origin for the degree to which generalized suppression of gene expression occurred upon introduction of dsRNA. As an assay, we tested the effects of dsRNA on the expression of GFP as measured in situ by counting fluorescent cells. As expected, in both human embryonic kidney cells (293) and mouse embryo fibroblasts, GFP expression was virtually eliminated irrespective of the sequence of the cotransfected dsRNA. In some pluripotent teratocarcinoma and teratoma cell lines (e.g., N-Teral, F9), the PKR response was attenuated but still evident; however, in contrast, transfection of nonhomologous dsRNAs had no effect on the expression of reporter genes (e.g., GFP or luciferase) either in mouse embryonic stem cells or in p19 embryonal carcinoma cells (FIG. 28).[0237]
• Transfection of P19 embryonal carcinoma cells with GFP in the presence of cognate dsRNA corresponding to the first ≈500 nts of the GFP coding sequence had a strikingly different effect. GFP expression was eliminated in the vast majority of cotransfected cells (FIG. 28), suggesting that these cultured murine cells might respond to dsRNA in a manner similar to that which we had previously demonstrated in cultured, Drosophila S2 cells (Hammond et al. 2000, Nature 404: 293-296).[0238]
• To quantify the extent to which dsRNA could induce sequence-specific gene silencing, we used a dual luciferase reporter assay similar to that which had first been used to demonstrate RNAi in Drosophila embryo extracts (Tuschl et al. 1999, Genes Dev. 13: 3191-3197). P19 EC cells were transfected with a mixture of two plasmids that individually direct the expression of firefly luciferase and Renilla luciferase. These were cotransfected with no dsRNA, with dsRNA that corresponds to the first ≈500 nts of the firefly luciferase, or with dsRNA corresponding to the first ≈500 nts of GFP as a control. Cotransfection with GFP dsRNA gave luciferase activities that were similar to the no-dsRNA control, both in the firefly/Renilla activity ratio and in the absolute values of both activities. In contrast, in cells that received the firefly luciferase dsRNA, the ratio of firefly to Renilla luciferase activity was reduced by up to 30-fold (250 ng, FIG. 29B). For comparison, we carried out an identical set of experiments in Drosophila S2 cells. Although qualitatively similar results were obtained, the silencing response was more potent. At equivalent levels of dsRNA, S2 cells suppressed firefly luciferase activity to virtually background levels.[0239]
• The complementary experiment, in which dsRNA was homologous to Renilla luciferase, was also performed. Again, in this case, suppression of the expression of the Renilla enzyme was ≈10-fold (FIG. 29D). Thus, the dsRNA response in P19 cells was flexible, and the silencing machinery was able to adapt to dsRNAs directed against any of the reporters that were tested.[0240]
• We took two approaches to test whether this response was specific for dsRNA. Pretreatment of the trigger with purified RNase III, a dsRNA-specific ribonuclease, before transfection greatly reduced its ability to provoke silencing. Furthermore, transfection of cells with single-stranded antisense RNAs directed against either firefly or Renilla luciferase had little or no effect on expression of the reporters (FIGS. 29C and 29D). Considered together, these results provided a strong indication that double-stranded RNAs provoke a potent and specific silencing response in P19 embryonal carcinoma cells. Efficient silencing could be provoked with relatively low concentrations of dsRNA (25 ng/ml culture media; see FIG. 29A). The response was concentration-dependent, with maximal suppression of ≈20-fold being achieved at a dose of 1.5 μg/ml culture media. Silencing was established rapidly and was evident by 9 h posttransfection (the earliest time point examined). Furthermore, the response persisted without significant changes in the degree of suppression for up to 72 h following a single dose of dsRNA.[0241]
• FIG. 30 further shows wildtype P19 cells which have been co-transfected with either RFP or GFP (right panel). Note the robust expression of RFP or GFR respectively approximately 42 hours post-transfection. We isolated P19 clones which stably express a 500 nt. GFP hairpin. Such clones were then transfected with either RFP or GFP, and expression of RFP or GFP was assessed by visual inspection of the cells. The left panel demonstrates that a 500 nt GFP hairpin specifically suppresses expression of GFP in P19 cells.[0242]
• B. RNAi in Embryonic Stem Cells.[0243]
• To assess whether the presence of a sequence-specific response to dsRNA was a peculiarity of P19 cells or whether it also extended to normal murine embryonic cells, we performed similar silencing assays in mouse embryonic stem cells. Cotransfection of embryonic stem cells with noncognate dsRNAs (e.g., GFP), again, had no dramatic effect on either the absolute values or the ratios of Renilla and firefly luciferase activity (FIG. 31). However, transfection with either firefly or Renilla luciferase dsRNA dramatically and specifically reduced the activity of the targeted enzyme (FIG. 31).[0244]
• This result suggests that RNAi can operate in multiple murine cell types of embryonic origin, including normal embryonic stem cells. The ability to provoke silencing in a cell type that is normally used for the generation of genetic, mosaic animals suggests the possibility of eventually testing the biological effects of silencing both in culture and in reconstituted animal models. Our ability to successfully manipulate ES cell via RNAi allows the use of RNAi in the generation of transgenic and knock-out mice.[0245]
• C. RNAI in Murine Somatic Cells.[0246]
• RNAi effector pathways are likely to be present in mammalian somatic cells, based on the ability of siRNAs to induce transient silencing (Elbashir et al. 2001, Nature 411: 494-498). Furthermore, we have shown that RNAi initiator and effector pathways clearly exist in embryonic cells that can enforce silencing in response to long dsRNA triggers. We therefore sought to test whether the RNAi machinery might exist intact in some somatic cell lines.[0247]
• Transfection of HeLa cells with luciferase reporters in combination with long dsRNA triggers caused a nearly complete suppression of activity, irrespective of the RNA sequence. In a murine myoblast cell line, C2C12, we noted a mixture of two responses. dsRNAs homologous to firefly luciferase provoked a sequence-specific effect, producing a degree of suppression that was slightly more potent than was observed upon transfection with cognate ≈21-nt siRNA (Elbashir et al. 2001, Nature 411: 494-498) (see FIG. 32A). However, with long dsRNA triggers, the specific effect was superimposed upon a generalized suppression of reporter gene expression that was presumably because of PKR activation (FIG. 32B).[0248]
• Numerous mammalian viruses have evolved the ability to block PKR as an aid to efficient infection. For example, adenoviruses express VA RNAs, which mimic dsRNA with respect to binding but not to activation of PKR (Clarke et al. 1995, RNA 1: 7-20). Vaccinia virus uses two strategies to evade PKR. The first is expression of E3L, which binds and masks dsRNAs (Kawagishi-Kobayashi et al. 2000, Virology 276: 424-434). The second is expression of K3L, which binds and inhibits PKR via its ability to mimic the natural substrate of this enzyme, eIF2α (Kawagishi-Kobayashi et al. 2000, supra).[0249]
• Transfection of C2C12 cells with a vector that directs K3L expression attenuates the generalized repression of reporter genes in response to dsRNA. However, this protein had no effect on the magnitude of specific inhibition by RNAi (FIG. 32C).[0250]
• FIG. 33 further shows the results of a transient co-transfection assay performed in Hela cells, CHO cells, and P19 cells. The cell lines were each transfected with plasmids expressing[0251]Photinus pyralis(firefly) andRenila reniformis(sea pansy) luciferases. The cells lines were additionally transfected with 400 ng of 500nt dsRNAs corresponding to either firefly luciferase (dsLUC) or dsGFP. The results demonstrate that dsRNA can specifically mediate suppression in a multiple mammalian cells types in culture.
• These results raise the possibility that, at least in some cell lines and/or cell types, blocking nonspecific responses to dsRNA will enable the use of long dsRNAs for the study of gene function. This might be accomplished through the use of viral inhibitors, as described here, or through the use of cells isolated from animals that are genetically modified to lack undesirable responses.[0252]
• D. Stable Suppression of Gene Expression Using RNAi.[0253]
• To date, dsRNAs have been used to induce sequence-specific gene silencing in either cultured mammalian cells or in embryos only in a transient fashion. However, the most powerful applications of genetic manipulation are realized only with the creation of stable mutants. The ability to induce silencing by using long dsRNAs offers the opportunity to translate into mammalian cells work from model systems such as Drosophila, plants, and[0254]C. eleganswherein stable silencing has been achieved by enforced expression of hairpin RNAs (Kennerdell et al. 2000, Nat. Biotechnol. 18: 896-898; Smith et al. 2000, Nature 407: 319-320; Tavemarakis et al. 2000, Nat. Genet. 24: 180-183).
• P19 EC cells were transfected with a control vector or with an expression vector that directs expression of a ≈500-nt GFP hairpin RNA from an RNA polymerase II promoter (cytomegalovirus). Colonies arising from cells that had stably integrated either construct were selected and expanded into clonal cell lines. Each cell line was assayed for persistent RNAi by transient cotransfection with a mixture of two reporter genes, dsRED to mark transfected cells and GFP to test for stable silencing.[0255]
• Transfection of clonal P19 EC cells that had stably integrated the control vector produced equal numbers of red and green cells, as would be expected in the absence of any specific silencing response (FIG. 34B), whereas cells that express the GFP hairpin RNA gave a very different result. These cells expressed the dsRED protein with an efficiency comparable to that observed in cells containing the control vector. However, the cells failed to express the cotransfected GFP reporter (FIG. 34B). These data provide a strong indication that continuous expression of a hairpin dsRNA can provoke stable, sequence-specific silencing of a target gene.[0256]
• In Drosophila S2 cells and[0257]C. elegans, RNAi is initiated by the Dicer enzyme, which processes dsRNA into ≈22-nt siRNAs (Bernstein et al. 2001, Nature 409: 363-366; Grishok et al. 2001, Cell 106: 23-34; Hutvagner et al. 2001, Science 293: 834-838; Ketting et al. 2001, Genes Dev. 15: 2654-2659; Knight et al. 2001, Science 293: 2269-2271). In both, S2 cells andC. elegansexperiments by using dsRNA to target Dicer suppress the RNAi response. Whether Dicer plays a central role in hairpin-induced gene silencing in P19 cells was tested by transfecting P19 cells stably transfected with GFP hairpin constructs with mouse Dicer dsRNA. Treatment with Dicer dsRNA, but not control dsRNA, resulted in derepression of GFP (FIG. 34C).
• E. dsRNA Induces Posttranscriptional Silencing.[0258]
• A key feature of RNAi is that it exerts its effect at the posttranscriptional level by destruction of targeted mRNAs (Hammond et al. 2001, Nat. Rev. Genet. 2: 110-119). To test whether dsRNAs induced silencing in mouse cells via posttranscriptional mechanisms, we used an assay identical to that, used initially to characterize RNAi responses in Drosophila embryo extracts (Tuschl et al. 1999, Genes Dev. 13: 3191-3197). We prepared lysates from P19 EC cells that were competent for in vitro translation of capped mRNAs corresponding to Renilla and firefly luciferase. Addition of nonspecific dsRNAs to these extracts had no substantial effect on either the absolute amount of luciferase expression or on the ratio of firefly to Renilla luciferase (FIG. 35). In contrast, addition of dsRNA homologous to the firefly luciferase induced a dramatic and dose-dependent suppression of activity. Addition of RNA corresponding to only the antisense strand of the dsRNA had little effect, comparable to a nonspecific dsRNA control, and pretreatment of the dsRNA silencing trigger with RNase III greatly reduced its potential to induce silencing in vitro. A second hallmark of RNAi is the production of small, ≈22-nt siRNAs, which determine the specificity of silencing. We found that such RNA species were generated from dsRNA in P19 cell extracts (FIG. 34D, in vitro), indicative of the presence of a mouse Dicer activity. These species were also produced in cells that stably express GFP hairpin RNAs (FIG. 34D, in vivo). Considered together, the posttranscriptional nature of dsRNA-induced silencing, the association of silencing with the production of ≈22-nt siRNAs, and the dependence of this response on Dicer, a key player in the RNAi pathway, strongly suggests that dsRNA suppresses gene expression in murine cells via a conventional RNAi mechanism.[0259]
• F RNAi-Mediated Gene Silencing is Specific and Requires dsRNAs.[0260]
• We carried out experiments to verify that the suppressive effects observed in the in vitro system were specific to double stranded RNA. Briefly, experiments were performed in accordance with the methods outlined above. Either dsRNA (ds), single-stranded RNA (ss), or antisense-RNA (as) corresponding to firefly (FF) or Renilla (Ren) luciferase was added to the translation reaction. Following reactions performed at 30° C. for 1 hour, dual luciferase assays were performed using an Analytical Scientific Instruments model 3010 Luminometer.[0261]
• FIG. 36 summarizes the results of these experiments which demonstrate that the suppression of gene expression observed in this in vitro assay is specific for dsRNA. These results further support the conclusion that dsRNA suppresses gene expression in this mammalian in vitro system in a manner consistent with post-transcriptional silencing.[0262]
• G. Mammalian Cells Soaked with dsRNAs Results in Gene Silencing.[0263]
• Studies of post-transcriptional silencing in invertebrates have demonstrated that transfection or injection of the dsRNA is not necessary to achieve the suppressive affects. For example, dsRNA suppression in[0264]C. eleganscan be observed by either soaking the worms in dsRNA, or by feeding the worms bacteria expressing the dsRNA of interest. We addressed whether dsRNA suppression in mammalian cells could be observed without transfection of the dsRNA. Such a result would present additional potential for easily using dsRNA suppression in mammalian cells, and would also allow the use of dsRNA to suppress gene expression in cell types which have been difficult to transfect (i.e., cell types with a low transfection efficiency, or cell types which have proven difficult to transfect at all).
• P19 cells were grown in 6-well tissue culture plates to approximately 60% confluency in growth media (αMEM/10% FBS). Varying concentrations of firefly dsRNA were added to the cultures, and cells were cultured for 12 hours in growth media+dsRNA. Cells were then transfected with plasmids expressing firefly or sea pansy luciferase, as described in detail above. Dual luciferase assays were carried out 12 hours post-transfection using an Analytical Scientific Instruments model 3010 Luminometer.[0265]
• FIG. 37 summarizes these results which demonstrate that dsRNA can suppress gene expression in mammalian cells without transfection. Culturing cells in the presence of dsRNA resulted in a dose dependent suppression of firefly luciferase gene expression.[0266]
• Methods:[0267]
• Cell Culture. P19 mouse embryonic carcinoma cells (American Type Culture Collection, CRL-1825) were cultured in α-MEM (GIBCO/BRL) supplemented with 10% heat-inactivated FBS and 1% antibiotic/antimycotic solution (GIBCO/BRL). Mouse embryo stem cells (J1, provided by S. Kim, Cold Spring Harbor Laboratory) were cultured in DMEM containing ESgro (Chemicon) according to the manufacturer's instructions. C2C12 murine myoblast cells (gift of N. Tonks, Cold Spring Harbor Laboratory) were cultured in DMEM (GIBCO/BRL) supplemented with 10% heat-inactivated FBS and 1% antibiotic/antimycotic solution (GIBCO/BRL).[0268]
• RNA Preparation. For the production of dsRNA, transcription templates were generated by PCR; they contained T7 promoter sequences on each end of the template (see Hammond et al. 2000, Nature 404: 293-296). dsRNAs were prepared by using the RiboMax kit (Ambion, Austin, Tex.). Firefly and Renilla luciferase mRNA transcripts were synthesized by using the Riboprobe kit (Promega) and were gel purified before use.[0269]
• Transfection and Gene Silencing Assays. Cells were transfected with indicated amounts of dsRNA and plasmid DNA by using FuGENE6 (Roche Biochemicals) according to the manufacturer's instructions. Cells were transfected at 50-70% confluence in 12-well plates containing either 1 or 2 ml of medium per well. Dual luciferase assays (Promega) were carried out by cotransfecting cells with plasmids contain firefly luciferase under the control of SV40 promoter (pGL3-Control, Promega) and Renilla luciferase under the control of the SV40 early enhancer/promoter region (pSV40, Promega). These plasmids were cotransfected by using a 1:1 or 10:1 ratio of pGL3-control (250 ng/well) to pRL-SV40. Both ratios yielded similar results. For some experiments, cells were transfected with vectors that direct expression of enhanced green fluorescent protein (EGFP)-US9 fusion protein (Kalejta et al. 1999, Exp. Cell Res. 248: 322-328) or red fluorescent protein (RFP) (pDsRed N1, CLONTECH). RNAi in S2 cells was performed as described (Hammond et al. 2000, Nature 404: 293-296).[0270]
• Plasmids expressing hairpin RNAs (RNAs with a self-complimentary stem loop) were constructed by cloning the first 500 bp of the EGFP coding region (CLONTECH) into the FLIP cassette of pRIP-FLIP as a direct repeat. The FLIP cassette contains two directional cloning sites, the second of which sports flanking LoxP sites (see FIG. 35A). The Zeocin gene (Stratagene), present between the cloning sites, maintains selection and, thus, stability of the FLIP cassette. The FLIP cassette containing EGFP direct repeats was subcloned into pcDNA3 (Invitrogen). To create an inverted repeat for hairpin production, EGFP direct repeat clones were exposed to Cre recombinase (Stratagene) in vitro and, afterward, transformed into DL759[0271]Escherichia coli(Connelly et al. 1996, Genes Cells 1: 285-291). These bacteria permit the replication of DNA containing cruciform structures, which tend to form from inverted repeats. DL759 transformants were screened for plasmids containing inverted repeats (≈50%).
• Silencing of Dicer was accomplished by using a[0272]dsRNA comprising exon 25 of the mouse Dicer gene and corresponding to nucleotides 5284-5552 of the human Dicer cDNA.
• In Vitro Translation and in Vitro Dicer Assays. Logarithmically growing cells were harvested in PBS containing 5 mM EGTA washed twice in PBS and once in hypotonic buffer (10 mM Hepes, pH 7.3/6 mM β-mercaptoethanol). Cells were suspended in 0.7 packed-cell volumes of hypotonic buffer containing Complete protease inhibitors (Roche Molecular Biochemicals) and 0.5 units/ml of RNasin (Promega). Cells were disrupted in a Dounce homogenizer with a type B pestle, and lysates were centrifuged at 30,000×g for 20 min. Supernatants were used in an in vitro translation assay containing capped m7G(5′)pppG firefly and Renilla luciferase mRNA or in in vitro Dicer assays containing[0273]³²P-labeled dsRNA. For in vitro translation assays, 5 μl of extract were mixed with 100 ng of firefly and Renilla mRNA along with 1 μg of dsRNA (or buffer)/10 mM DTT/0.5 mM spermidine/200 mM Hepes, 3.3 mM MgOAc/800 mM KOAc/1 mM ATP/1 mM GTP/4 units of Rnasin/215 μg of creatine phosphate/1 μg of creatine phosphate kinase/1 mM amino acids (Promega). Reactions were carried out for 1 h at 30° C. and quenched by adding 1× passive lysis buffer (Promega). Extracts were then assayed for luciferase activity. In vitro assays for Dicer activity were performed as described (Bernstein et al. 2001, Nature 409: 363-366).
• Construction of Stable Silencing Lines. Ten-centimeter plates of P19 cells were transfected with 5 μg of GFP hairpin expression plasmid and selected for stable integrants by using G-418 (300 ng/ml) for 14 days. Clones were selected and screened for silencing of GFP.[0274]
EXAMPLE 5Compositions and Methods for Synthesizing siRNAs
• Previous results have indicated that short synthetic RNAs (siRNAs) can efficiently induce RNA suppression. Since short RNAs do not activate the non-specific PKR response, they offer a means for efficiently silencing gene expression in a range of cell types. However, the current state of the art with respect to siRNAs has several limitations. Firstly, siRNAs are currently chemically synthesized at great cost (approx. $400/siRNA). Such high costs make siRNAs impractical for either small laboratories or for use in large scale screening efforts. Accordingly, there is a need in the art for methods for generating siRNAs at reduced cost.[0275]
• We provide compositions and methods for synthesizing siRNAs by T7 polymerase. This approach allows for the efficient sythesis of siRNAs at a cost consistent with standard RNA transcription reactions (approx. $16/siRNA). This greatly reduced cost makes the use of siRNA a reasonable approach for small laboratories, and also will facilitate their use in large-scale screening projects.[0276]
• FIG. 38 shows the method for producing siRNAs using T7 polymerase. Briefly, T7 polymerase is used to transcribe both a sense and antisense transcript. The transcripts are then annealed to provide an siRNA. One of skill in the art will recognize that any one of the available RNA polymerases can be readily substituted for T7 to practice the invention (i.e., T3, Sp6, etc.).[0277]
• This approach is amenable to the generation of a single siRNA species, as well as to the generation of a library of siRNAs. Such a library of siRNAs can be used in any number of high-throughput screens including cell based phenotypic screens and gene array based screens.[0278]
EXAMPLE 6Generation of Short Hairpin dsRNA and Suppression of Gene Expression Using Such Short Hairpins
• Since the realization that small, endogenously encoded hairpin RNAs could regulate gene expression via elements of the RNAi machinery, we have sought to exploit this biological mechanism for the regulation of desired target genes. Here we show that short hairpin RNAs (shRNAs) can induce sequence-specific gene silencing in mammalian cells. As is normally done with siRNAs, silencing can be provoked by transfecting exogenously synthesized hairpins into cells. However, silencing can also be triggered by endogenous expression of shRNAs. This observation opens the door to the production of continuous cells lines in which RNAi is used to stably suppress gene expression in mammalian cells. Furthermore, similar approaches should prove efficacious in the creation of transgenic animals and potentially in therapeutic strategies in which long-term suppression of gene function is essential to produce a desired effect.[0279]
• Several groups (Grishok et al. 2001, Cell 106: 23-34; Ketting et al. 2001, Genes & Dev. 15: 2654-2659; Knight et al. 2001, Science 293: 2269-2271; Hutvagner et al. 2001, Science 293: 834-838) have shown that endogenous triggers of gene silencing, specifically small temporal RNAs (stRNAs) let-7 and lin-4, function at least in part through RNAi pathways. Specifically, these small RNAs are encoded by hairpin precursors that are processed by Dicer into mature, ˜21-nt forms. Moreover, genetic studies in[0280]C. eleganshave shown a requirement for Argonaute-family proteins in stRNA function. Specifically, alg-1 and alg-2, members of the EIF2c subfamily, are implicated both in stRNA processing and in their downstream effector functions (Grishok et al., 2001, supra). We have recently shown that a component of RISC, the effector nuclease of RNAi, is a member of the Argonaute family, prompting a model in which stRNAs may function through RISC-like complexes, which regulate mRNA translation rather than mRNA stability (Hammond et al. 2001, Science 293: 1146-1150).
• A. Short Hairpin RNAs Triggeedr Gene Silencing in Drosophila Cells.[0281]
• We wished to test the possibility that we might retarget these small, endogenously encoded hairpin RNAs to regulate genes of choice with the ultimate goal of subverting this regulatory system for manipulating gene expression stably in mammalian cell lines and in transgenic animals. Whether triggered by long dsRNAs or by siRNAs, RNAi is generally more potent in the suppression of gene expression in Drosophila S2 cells than in mammalian cells. We therefore chose this model system in which to test the efficacy of short hairpin RNAs (shRNAs) as inducers of gene silencing.[0282]
• Neither stRNAs nor the broader group of miRNAs that has recently been discovered form perfect hairpin structures. Indeed, each of these RNAs is predicted to contain several bulged nucleotides within their rather short (˜30-nt) stem structures. Because the position and character of these bulged nucleotides have been conserved throughout evolution and among at least a subset of miRNAs, we sought to design retargeted miRNA mimics to conserve these predicted structural features. Only the let-7 and lin-4 miRNAs have known miRNA targets (Wightman et al. 1993, Cell 75: 855-862; Slack et al. 2000, Mol. Cell 5: 659-669). In both cases, pairing to binding sites within the regulated transcripts is imperfect, and in the case of lin-4, the presence of a bulged nucleotide is critical to suppression (Ha et al. 1996, Genes & Dev. 10: 3041-3050). We therefore also designed shRNAs that paired imperfectly with their target substrates. A subset of these shRNAs is depicted in FIG. 39A.[0283]
• To permit rapid testing of large numbers of shRNA variants and quantitative comparison of the efficacy of suppression, we chose to use a dual-luciferase reporter system, as previously described for assays of RNAi in both Drosophila extracts (Tuschl et al. 1999, Genes & Dev. 13: 3191-3197) and mammalian cells (Caplen et al. 2001, Proc. Natl. Acad. Sci. 98: 9742-9747; Elbashir et al., 2001, Nature 411: 494-498). Cotransfection of firefly and Renilla luciferase reporter plasmids with either long dsRNAs or with siRNAs homologous to the firefly luciferase gene yielded an ˜95% suppression of firefly luciferase without effect on Renilla luciferase (FIG. 39B; data not shown). Firefly luciferase could also be specifically silenced by cotransfection with homologous shRNAs. The most potent inhibitors were those composed of simple hairpin structures with complete homology to the substrate. Introduction of G-U basepairs either within the stem or within the substrate recognition sequence had little or no effect (FIGS. 39A and 39B; data not shown).[0284]
• These results show that short hairpin RNAs can induce gene silencing in Drosophila S2 cells with potency similar to that of siRNAs (FIG. 39B). However, in our initial observation of RNA interference in Drosophila S2 cells, we noted a profound dependence of the efficiency of silencing on the length of the dsRNA trigger (Hammond et al. 2000, Nature 404: 293-296). Indeed, dsRNAs of fewer than ˜200 nt triggered silencing very inefficiently. Silencing is initiated by an RNase III family nuclease, Dicer, that processes long dsRNAs into ˜22-nt siRNAs. In accord with their varying potency as initiators of silencing, long dsRNAs are processed much more readily than short RNAs by the Dicer enzyme (Bernstein et al. 2001, Nature 409: 363-366). We therefore tested whether shRNAs were substrates for the Dicer enzyme.[0285]
• We had noted previously that let-7 (Ketting et al. 2001, Genes & Dev. 15: 2654-2659) and other miRNAs (E. Bernstein, unpublished data) are processed by Dicer with an unexpectedly high efficiency as compared with short, nonhairpin dsRNAs. Similarly, Dicer efficiently processed shRNAs that targeted firefly luciferase, irrespective of whether they were designed to mimic a natural Dicer substrate (let-7) or whether they were simple hairpin structures (FIG. 39C). These data suggest that recombinant shRNAs can be processed by Dicer into siRNAs and are consistent with the idea that these short hairpins trigger gene silencing via an RNAi pathway.[0286]
• B. Short Hairpin RNAs Activated Gene Silencing in Mammalian Cells.[0287]
• Mammalian cells contain several endogenous systems that were predicted to hamper the application of RNAi. Chief among these is a dsRNA-activated protein kinase, PKR, which effects a general suppression of translation via phosphorylation of EIF-2α (Williams 1997, Biochem. Soc. Trans. 25: 509-513; Gil et al. 2000, Apoptosis 5: 107-114). Activation of these, and other dsRNA-responsive pathways, generally requires duplexes exceeding 30 bp in length, possibly to permit dimerization of the enzyme on its allosteric activator (e.g., Clarke et al. 1995, RNA 1: 7-20). Small RNAs that mimic Dicer products, siRNAs, presumably escape this limit and trigger specific silencing, in part because of their size. However, short duplex RNAs that lack signature features of siRNAs can efficiently induce silencing in Drosophila S2 cells but not in mammalian cells (A. A. Caudy, unpublished data). Endogenously encoded miRNAs may also escape PKR surveillance because of their size but perhaps also because of the discontinuity of their duplex structure. Given that shRNAs of <30 bp were effective inducers of RNAi in Drosophila S2 cells, we tested whether these RNAs could also induce sequence-specific silencing in mammalian cells.[0288]
• Human embryonic kidney (HEK293T) cells were cotransfected with chemically synthesized shRNAs and with a mixture of firefly and Renilla luciferase reporter plasmids. As had been observed in S2 cells, shRNAs were effective inducers of gene silencing. Once again, hairpins designed to mimic let-7 were consistently less effective than were simple hairpin RNAs, and the introduction of mismatches between the antisense strand of the shRNA and the mRNA target abolished silencing (FIG. 40A; data not shown). Overall, shRNAs were somewhat less potent silencing triggers than were siRNAs. Whereas siRNAs homologous to firefly luciferase routinely yielded ˜90%-95% suppression of gene expression, suppression levels achieved with shRNAs ranged from 80%-90% on average. As we also observe with siRNAs, the most important determinant of the potency of the silencing trigger is its sequence. We find that roughly 50% of both siRNAs and shRNAs are competent for suppressing gene expression. However, neither analysis of the predicted structures of the target mRNA nor analysis of alternative structures in siRNA duplexes or shRNA hairpins has proved of predictive value for choosing effective inhibitors of gene expression.[0289]
• We have adopted as a standard, shRNA duplexes containing 29 bp. However, the size of the helix can be reduced to ˜25 nt without significant loss of potency. Duplexes as short as 22 bp can still provoke detectable silencing, but do so less efficiently than do longer duplexes. In no case did we observe a reduction in the internal control reporter (Renilla luciferase) that would be consistent with an induction of nonspecific dsRNA responses.[0290]
• The ability of shRNAs to induce gene silencing was not confined to 293T cells. Similar results were also obtained in a variety of other mammalian cell lines, including human cancer cells (HeLa), transformed monkey epithelial cells (COS-1), murine fibroblasts (NIH 3T3), and diploid human fibroblasts (IMR90; FIG. 40; data not shown).[0291]
• C. Synthesis of Effective Inhibitors of Gene Expression Using T7 RNA Polymerse.[0292]
• The use of siRNAs to provoke gene silencing is developing into a standard methodology for investigating gene function in mammalian cells. To date, siRNAs have been produced exclusively by chemical synthesis (e.g., Caplen et al. 2001, Proc. Natl. Acad. Sci. 98: 9742-9747; Elbashir et al. 2001, Nature 411: 494-498). However, the costs associated with this approach are significant, limiting its potential utility as a tool for investigating in parallel the functions of large numbers of genes. Short hairpin RNAs are presumably processed into active siRNAs in vivo by Dicer. Thus, these may be more tolerant of terminal structures, both with respect to nucleotide overhangs and with respect to phosphate termini. We therefore tested whether shRNAs could be prepared by in vitro transcription with T7 RNA polymerase.[0293]
• Transcription templates that were predicted to generate siRNAs and shRNAs similar to those prepared by chemical RNA synthesis were prepared by DNA synthesis (FIG. 41A,C). These were tested for efficacy both in S2 cells (data not shown) and in human 293 cells (FIG. 41B,D). Overall, the performance of the T7-synthesized hairpin or siRNAs closely matched the performance of either produced by chemical synthesis, both with respect to the magnitude of inhibition and with respect to the relative efficiency of differing sequences. Because T7 polymerase prefers to initiate at twin guanosine residues, however, it was critical to consider initiation context when designing in vitro transcribed siRNAs (FIG. 41B). In contrast, shRNAs, which are processed by Dicer (see FIG. 39C), tolerate the addition of these bases at the 5′ end of the transcript.[0294]
• Studies in Drosophila embryo extracts indicate that siRNAs possess 5′ phosphorylated termini, consistent with their production by an RNase III family nuclease. In vitro, this terminus is critical to the induction of RNAi by synthetic RNA oligonucleotides (Elbashir et al. 2001, EMBO J. 20: 6877-6888; Nykanen et al. 2001, Cell 107: 309-321). Chemically synthesized siRNAs are nonphosphorylated, and enzymatic addition of a 5′ phosphate group in vitro prior to transfection does not increase the potency of the silencing effect (A. A. Caudy, unpublished data). This suggests either that the requirement for phosphorylated termini is less stringent in mammalian cells or that a kinase efficiently phosphorylates siRNAs in vivo. RNAs synthesized with T7 RNA polymerase, however, possess 5′ triphosphate termini. We therefore explored the possibility of synthesizing siRNAs with T7 polymerase followed by treatment in vitro with pyrophosphatase to modify the termini to resemble those of siRNAs. Surprisingly, monophosphorylated siRNAs (data not shown) were as potent in inducing gene silencing as transcription products bearing triphosphate termini (FIG. 41B). This may suggest either that the requirement for monophosphorylated termini is less stringent in mammalian cells or that siRNAs are modified in vivo to achieve an appropriate terminal structure.[0295]
• Considered together, our data suggest that both shRNAs and siRNA duplexes can be prepared by synthesis with T7 RNA polymerase in vitro. This significantly reduces the cost of RNAi in mammalian cells and paves the way for application of RNAi on a whole-genome scale.[0296]
• D. Transcription of Small Hairpin RNAs In Vivo by RNA Polymerase III.[0297]
• Although siRNAs are an undeniably effective tool for probing gene function in mammalian cells, their suppressive effects are by definition of limited duration. Delivery of siRNAs can be accomplished by any of a number of transient transfection methodologies, and both the timing of peak suppression and the recovery of protein levels as silencing decays can vary with both the cell-type and the target gene. Therefore, one limitation on siRNAs is the development of continuous cell lines in which the expression of a desired target is stably silenced.[0298]
• Hairpin RNAs, consisting of long duplex structures, have been proved as effective triggers of stable gene silencing in plants, in[0299]C. elegans, and in Drosophila (Kennerdell et al. 2000, Nat. Biotechnol. 18: 896-898; Smith et al. 2000, Nature 407: 319-320; Tavernarakis et al. 2000, Nat. Genet. 24: 180-183). We have recently shown stable suppression of gene expression in cultured mammalian cells by continuous expression of a long hairpin RNA (Paddison et al. 2002, Proc. Natl. Acad. Sci. 99: 1443-1448). However, the scope of this approach was limited by the necessity of expressing such hairpins only in cells that lack a detectable PKR response. In principle, shRNAs could bypass such limitations and provide a tool for evoking stable suppression by RNA in mammalian somatic cells.
• To test this possibility, we initially cloned sequences encoding a firefly luciferase shRNA into a CMV-based expression plasmid. This was predicted to generate a capped, polyadenylated RNA polymerase II transcript in which the hairpin was extended on both the 5′ and 3′ ends by vector sequences and poly(A). This construct was completely inert in silencing assays in 293T cells.[0300]
• During our studies on chemically and T7-synthesized shRNAs, we noted that the presence of significant single-stranded extensions (either 5′ or 3′ of the duplex) reduced the efficacy of shRNAs. We therefore explored the use of alternative promoter strategies in an effort to produce more defined hairpin RNAs. In particular, RNA polymerase III promoters have well-defined initiation and termination sites and naturally produce a variety of small, stable RNA species. Although many Pol III promoters contain essential elements within the transcribed region, limiting their utility for our purposes; class III promoters use exclusively nontranscribed promoter sequences. Of these, the U6 snRNA promoter and the H1 RNA promoter have been well studied (Lobo et al. 1990, Nucleic Acids Res. 18: 2891-2899; Hannon et al. 1991, J. Biol. Chem. 266: 22796-22799; Chong et al. 2001, J. Biol. Chem. 276: 20727-20734).[0301]
• By placing a convenient cloning site immediately behind the U6 snRNA promoter, we have constructed pShh-1, an expression vector in which short hairpins are harnessed for gene silencing. Into this vector either of two shRNA sequences derived from firefly luciferase were cloned from synthetic oligonucleotides. These were cotransfected with firefly and Renilla luciferase expression plasmids into 293T cells. One of the two encoded shRNAs provoked effective silencing of firefly luciferase without altering the expression of the internal control (FIG. 42C). The second encoded shRNA also produced detectable, albeit weak, repression. In both cases, silencing was dependent on insertion of the shRNA in the correct orientation with respect to the promoter (FIG. 42C; data not shown). Although the shRNA itself is bilaterally symmetric, insertion in the incorrect orientation would affect Pol III termination and is predicted to produce a hairpin with both 5′ and 3′ single-stranded extensions. Similar results were also obtained in a number of other mammalian cell lines including HeLa, COS-1, NIH 3T3, and IMR90 (FIG. 42; data not shown). pShh1-Ff1 was, however, incapable of effecting suppression of the luciferase reporter in Drosophila cells, in which the human U6 promoter is inactive.[0302]
• E. Dicer is Required for shRNA-Mediated Gene Silencing.[0303]
• As a definitive test of whether the plasmid-encoded shRNAs brought about gene silencing via the mammalian RNAi pathway, we assessed the dependence of suppression on an essential component of the RNAi pathway. We transfected pShh1-Ff1 along with an siRNA homologous to human Dicer. FIG. 43 shows that treatment of cells with Dicer siRNAs is able to completely depress the silencing induced by pShh1-Ff1. Addition of an unrelated siRNA had no effect on the magnitude of suppression by pShh1-Ff1. Importantly, Dicer siRNAs had no effect on siRNA-induced silencing of firefly luciferase. These results are consistent with shRNAs operating via an RNAi pathway similar to those provoked by stRNAs and long dsRNAs. Furthermore, it suggests that siRNA-mediated silencing is less sensitive to depletion of the Dicer enzyme.[0304]
• F. Stable shRNA-Mediated Gene Silencing of an Endogenous Gene.[0305]
• The ultimate utility of encoded short hairpins will be in the creation of stable mutants that permit the study of the resulting phenotypes. We therefore tested whether we could create a cellular phenotype through stable suppression. Expression of activated alleles of the ras oncogene in primary mouse embryo fibroblasts (MEFs) induces a stable growth arrest that resembles, as a terminal phenotype, replicative senescence (Serrano et al. 1997, Cell 88: 593-602). Cells cease dividing and assume a typical large, flattened morphology. Senescence can be countered by mutations that inactivate the p53 tumor suppressor pathway (Serrano et al. 1997, supra). As a test of the ability of vector-encoded shRNAs to stably suppress an endogenous cellular gene, we generated a hairpin that was targeted to the mouse p53 gene. As shown in FIG. 44, MEFs transfected with pBabe-RasV12 fail to proliferate and show a senescent morphology when cotransfected with an empty control vector. As noted previously by Serrano et al., the terminally arrested state is achieved in 100% of drug-selected cells in culture by 8 d posttransfection. However, upon cotransfection of an activated ras expression construct with the pShh-p53, cells emerged from drug selection that not only fail to adopt a senescent morphology but also maintain the ability to proliferate for a minimum of several weeks in culture (FIG. 44). These data strongly suggest that shRNA expression constructs can be used for the creation of continuous mammalian cell lines in which selected target genes are stably suppressed.[0306]
• G. Simultaneous Introduction of Multiple Hairpin RNAs Does Not Produce Synergy.[0307]
• In an attempt to further understand the mechanisms by which short hairpins suppress gene expression, we examined the effects of transfecting cells with a mixture of two different short hairpins corresponding to firefly luciferase. FIG. 45 summarizes the results of experiments which suggest that there is no synergistic affects on suppression of firefly luciferase gene expression obtained when cells are exposed to a mixture of such short hairpins.[0308]
• Methods:[0309]
• Cell culture.[0310]HEK 293T, HeLa, COS-1, MEF, and IMR90 cells were cultured in DMEM (GIBCO BRL) supplemented with 10% heat-inactivated fetal bovine serum (FBS) and 1% antibiotic/antimycotic solution (GIBCO BRL). NIH 3T3 cells were cultured in DMEM supplemented with 10% heat-inactivated calf serum and 1% antibiotic/antimycotic solution.
• RNA preparation. Both shRNAs and siRNAs were produced in vitro using chemically synthesized DNA oligonucleotide templates (Sigma) and the T7 Megashortscript kit (Ambion). Transcription templates were designed such that they contained T7 promoter sequences at the 5′ end. shRNA transcripts subjected to in vitro Dicer processing were synthesized using a Riboprobe kit (Promega). Chemically synthesized RNAs were obtained from Dharmacon, Inc.[0311]
• Transfection and gene silencing assays. Cells were transfected with indicated amounts of siRNA, shRNA, and plasmid DNA using standard calcium phosphate procedures at 50%-70% confluence in 6-well plates. Dual luciferase assays (Promega) were carried out by cotransfecting cells with plasmids containing firefly luciferase under the control of the SV40 promoter (pGL3-Control, Promega) and Renilla luciferase under the control of the SV40 early enhancer/promoter region (pSV40, Promega). Plasmids were cotransfected using a 1:1 ratio of pGL3-Control (250 ng/well) to pRL-SV40. RNAi in S2 cells was performed as previously described (Hammond et al., 2000, Nature 404: 293-296). For stable silencing, primary MEFs (a gift from S. Lowe, Cold Spring Harbor Laboratory, NY) were cotransfected using[0312]Fugene 6 with pBabe-Ha-rasV12 and pShh-p53 (no resistance marker), according to the manufacturer's recommendations. Selection was for the presence of the activated Ha-rasV12 plasmid, which carries a puromycin-resistance marker. The pShh-p53 plasmid was present in excess, as is standard in a cotransfection experiment. We have now generated a version of the U6 promoter vector (pSHAG-1) that is compatible with the GATEWAY system (Invitrogen), and this can be used to transport the shRNA expression cassette into a variety of recipient vectors that carry cis-linked selectable markers. Furthermore, we have validated delivery of shRNAs using retroviral vectors. Updated plasmid information can be obtained at http://www.cshl.org/public/science/hannon.html.
• Plasmids expressing hairpin RNAs. The U6 promoter region from −265 to +1 was amplified by PCR, adding 5′ KpnI and 3′ EcoRV sites for cloning into pBSSK+. A linker/terminator oligonucleotide set bearing the U6 terminator sequence and linker ends of 5′ EcoRV and 3′ NotI was cloned into the promoter construct, resulting in a U6 cassette with an EcoRV site for insertion of new sequences. This vector has been named pShh1. Blunt-ended, double-stranded DNA oligonucleotides encoding shRNAs with between 19 and 29 bases of homology to the targeted gene were ligated into the EcoRV site to produce expression constructs. The oligonucleotide sequence used to construct Ff1 was: TCCAATTCAGCGGGAGCCACCTGATGAAGCTTGATCGGGTGGCTCTCGCTGAG TTGGAATCCATTTTTTTT. This sequence is preceded by the sequence GGAT, which is supplied by the vector, and contains a tract of more than five Ts as a Pol III terminator.[0313]
• In vitro Dicer assays. In vitro assays for Dicer activity were performed as described (Bernstein et al., 2001, Nature 409: 363-366).[0314]
EXAMPLE 7Encoded Short Hairpins Function in Vivo
• An object of the present invention is to improve methods for generating siRNAs and short hairpins for use in specifically suppressing gene expression. Example 6 demonstrates that siRNAs and short hairpins are highly effective in specifically suppressing gene expression. Accordingly, it would be advantageous to combine the efficient suppression of gene expression attainable using short hairpins and siRNAs with a method to encode such RNA on a plasmid and express it either transiently or stably.[0315]
• FIG. 46 demonstrates that short hairpins encoded on a plasmid are effective in suppressing gene expression. DNA oligonucleotides encoding 29 nucleotide hairpins corresponding to firefly luciferase were inserted into a vector containing the U6 promoter. Three independent constructs were examined for their ability to specifically suppress firefly luciferase gene expression in 293T cells. siOligo1-2, siOligo1-6, and siOligo1-19 (construct in the correct orientation) each suppressed gene expression as effectively as siRNA. In contrast, siOligo1-10 (construct in the incorrect orientation) did not suppress gene expression. Additionally, an independent construct targeted to a different portion of the firefly luciferase gene did not effectively suppress gene expression in either orientation (siOligo2-23, siOligo2-36).[0316]
• The results summarized in FIG. 46 demonstrate that transient expression of siRNAs and short hairpins encoded on a plasmid can efficiently suppress gene expression. One of skill can choose from amongst a range of vectors to either transiently or stably express an siRNA or short hairpin. Non-limiting examples of vectors and strategies to stably express short dsRNAs are presented in FIGS.[0317]47-49.
EXAMPLE 8dsRNA Suppression in the Absence of a PKR Response
• One potential impediment to the use of RNAi to suppress gene expression in some cell types, is the non-specific PKR response that can be triggered by long dsRNAs. Numerous mammalian viruses have evolvd the ability to block PKR inorder to aid in the infection of potential host cells. For example, adenoviruses express RNAs which mimic dsRNA but do not activate the PKR response. Vaccinia virus uses two strategies to evade PKR: the expression of E3L which binds and masks dsRNA; the expression of K3L to mimic the natural PKR substrate eIF2α.[0318]
• Our understanding of the mechanisms by which viruses avoid the PKR response allows us to design approaches to circumvent the PKR response in cell types in which in might be advantageous to suppression gene expression with long dsRNAs. Possible approaches include treating cells with an agent that inhibits protein kinase RNA-activated (PKR) apoptosis, such as by treatment with agents which inhibit expression of PKR, cause its destruction, and/or inhibit the kinase activity of PKR. Accordingly, RNAi suppression of gene expression in such cell types could involve first inhibiting the PKR response, and then delivering a dsRNA identical or similar to a target gene.[0319]
• A. In a murine myoblast cell line, C2C12, we noted that the cells responded to long dsRNAs with a mixture of specific and non-specific (presumably PKR) responses. In order to attenuate the non-specific PKR response while maintaining the robust and specific suppression due to the long dsRNA, C2C12 cells were transfected with a vector that directs K3L expression. This additional step successfully attenuated the PKR response, however expression of K3L protein had no effect on the magnitude of specific inhibition.[0320]
• B. However, since the efficacy of such a two step approach had not been previously demonstrated, it was formerly possible that dsRNA suppression would not be possible in cells with a PKR response. FIG. 50 summarizes results which demonstrate that such a two step approach is possible, and that robust and specific dsRNA mediated suppression is possible in cells which had formerly possessed a robust PKR response.[0321]
• Briefly, dual luciferase assay were carried out as described in detail above. The experiments were carried out using PKR−/− MEFs harvested from E13.5 PKR−/− mosue embryos. MEFs typically have a robust PKR response, and thus treatment with long dsRNAs typically results in non-specific suppression of gene expression and apoptosis. However, in PKR−/− cells examined 12, 42, and 82 hours after transfection, expression of dsRenilla luciferase RNA specifically suppresses expression[0322]Renilla reniformis(sea pansy) luciferase. This suppression is stable over time.
• These results demonstrate that the non-specific PKR response can be blocked without affecting specific suppression of gene expression mediated by dsRNA. This allows the use of long dsRNAs to suppress gene expression in a diverse range of cell types, including those that would be previously intractable due to the confounding influences of the non-specific PKR response to long dsRNA.[0323]
EXAMPLE 9Suppression of Gene Expression Using dsRNA which Corresponds to Non-Coding Sequence
• Current models for the mechanisms which drive RNAi have suggested that the dsRNA construct must contain coding sequence corresponding to the gene of interest. Although evidence has demonstrated that such coding sequence need not be a perfect match to the endogenous coding sequence (i.e., it may be similar), it has been widely held that the dsRNA construct must correspond to coding sequence. We present evidence that contradicts the teachings of the prior art, and demonstrate that dsRNA corresponding to non-coding regions of a gene can suppress gene function in vivo. These results are significant not only because they demonstrate that dsRNA identical or similar to non-coding sequences (i.e., promoter sequences, enhancer sequences, or intronic sequences) can mediate suppression, but also because we demonstrate the in vivo suppression of gene expression using dsRNA technology in a mouse model.[0324]
• We generated doubled stranded RNA corresponding to four segments of the mouse tyrosinase gene promoter. Three of these segments correspond to the proximal promoter and one corresponds to an enhancer (FIG. 51). The tyrosinase gene encodes the rate limiting enzyme involved in the melanin biosynthetic pathway (Bilodeau et al. (2001)[0325]Pigment Cell Research14: 328-336). Accordingly, suppression of the tyrosinase gene is expected to inhibit pigmentation.
• Double stranded RNA corresponding to each of the above promoter segments was injected into the pronuclei of fertilized eggs. Pups were born after 19 days. In total 42/136 (31%) of the embryos were carried to term. This number is within the expected range for transgenesis (30-40%). Two pups out of 42 (5%) appear totally unpigmented at birth, consistent with suppression of tyrosinase function.[0326]
• Methods:[0327]
• dsRNA from non-coding promoter region of tyrosinase gene. Four segments of the mouse tyrosinase gene promoter were amplified by PCR using primers which incorporated T7 RNA polymerase promoters into the PCR products (shown in bold—FIG. 51). Sequences of the[0328]mouse tyrosinase gene 5′ flanking regions were obtained from GenBank (accession number D00439 and X51743). The sequence of the tyrosinase enhancer, located approximately 12 kb upstream of the transcriptional start site, was also obtained from GenBank (accession number X76647).
• The sequences of the primers used were as follows: note the sequence of the T7 RNA polymerase promoter is shown in bold[0329]

  (a) Tyrosinase enhancer (˜12 kb upstream):
  5′TAATACGACTCACTATAGGGCAAGGTCATAGTTCCTGCCAGCTG 3′
  5′TAATACGACTCACTATAGGGCAGATATTTTCTTACCACCCACCC 3′
  (b) −1404 to −1007:
  5′TAATACGACTCACTATAGGGTTAAGTTTAACAGGAGAAGCTGGA 3′
  5′TAATACGACTCACTATAGGGAAATCATTGCTTTCCTGATAATGC 3′
  (c) −1003 to −506:
  5′TAATACGACTCACTATAGGGTAGATTTCCGCAGCCCCAGTGTTC 3′
  5′TAATACGACTCACTATAGGGGTTGCCTCTCATTTTTCCTTGATT 3′
  (d) −505 to −85:
  5′TAATACGACTCACTATAGGGTATTTTAGACTGATTACTTTTATAA 3′
  5′TAATACGACTCACTATAGGGTCACATGTTTTGGCTAAGACCTAT 3′

• PCR products were gel purified from 1% TAE agarose gels using QiaExII Gel Extraction Kit (Qiagen). Double stranded RNA was produced from these templates using T7-Megashortscript Kit (Ambion). Enzymes and unincorporated nucleotides were removed using Qiaquick MinElute PCR Purification Kit. RNA was phenol/chloroform extracted twice, and ethanol precipitated. Pellets were resuspended in injection buffer ((10 mM Tris (pH 7.5), 0.15 nM EDTA (pH 8.0)) at a concentration of 20 ng/ul and run on a 1% TAE agarose gel to confirm integrity.[0330]
• Generation of mice: An equal mixture of double stranded RNA from each of the above primer sets was injected into the pronuclei of fertilized eggs from C57BL6J mice. A total of 136 injections was performed, and 34 embryos were implanted into each of 4 pseudopregnant CD-1 females. Pups were born after 19 days. In total, 42/136 (31%) of the embryos were carried to term. 2/42 pups (5%) appear totally unpigmented at birth.[0331]
• It is not clear whether the RNAi mediated by dsRNA identical or similar to non-coding sequence works via the same mechanism as PTGS observed in the presence of dsRNA identical or similar to coding sequence. However, whether these results ultimately reveal similar or differing mechanisms does not diminish the tremendous utility of the compositions and methods of the present invention to suppress expression of one or more genes in vitro or in vivo.[0332]
• The present invention demonstrates that dsRNA ranging in length from 20-500 nt can readily suppress expression of target genes both in vitro and in vivo. Furthermore, the present invention demonstrates that the dsRNAs can be generated using a variety of methods including the formation of hairpins, and that these dsRNAs can be expressed either stably or transiently. Finally, the present invention demonstrates that dsRNA identical or similar to non-coding sequences can suppress target gene expression.[0333]
EXAMPLE 10RNA Interference in Adult Mice
• RNA interference is an evolutionarily conserved surveillance mechanism that responds to double-stranded RNA by sequence-specific silencing of homologous genes. Here we show that transgene expression can be suppressed in adult mice by synthetic small interfering RNAs and by small-hairpin RNAs transcribed in vivo from DNA templates. We also show the therapeutic potential of this technique by demonstrating effective targeting of a sequence from hepatitis C virus by RNA interference in vivo.[0334]
• Small interfering RNAs (siRNAs) mimic intermediates in the RNA-interference (RNAi) pathway and can silence genes in somatic cells without activating non-specific suppression by double-stranded RNA-dependent protein kinase (Elbashir et al. 2001, Nature 411: 494-498). To investigate whether siRNAs also inhibit gene expression in vivo, we used a modification of hydrodynamic transfection methods (Zhang et al. 1999, Hum. Gene Therapy 10: 1735-1737; Liu et al. 1999, Gene Therapy 6: 1258-1266; Chang et al. 2001, J. Virol. 75: 3469-3473) to deliver naked siRNAs to the livers of adult mice. Either an siRNA derived from firefly luciferase or an unrelated siRNA was co-injected with a luciferase-expression plasmid (for construct description and sequences, see FIG. 52). We monitored luciferase expression in living animals using quantitative whole-body imaging (Contag, et al. 1997, Photochem. Photobiol. 66: 523-531) (see FIGS. 53[0335]a,54a), and found that it was dependent on reporter-plasmid dose.
• In each experiment, serum measurements of a co-injected human χ-1 antitrypsin (hAAT) plasmid (Yant et al. 2000, Nature Genet. 25: 35-41) served to normalize transfection efficiency and to monitor non-specific translational inhibition. Average serum concentrations of HAAT after 74 h were similar in all groups.[0336]
• Our results indicate that there was specific, siRNA-mediated inhibition of luciferase expression in adult mice (P<0.0115) and that unrelated siRNAs had no effect (P<0.864; FIGS. 53[0337]a,53b). In 11 independent experiments, luciferase siRNAs reduced luciferase expression (as judged by emitted light) by an average of 81% (±2.2%). These findings indicate that RNAi can downregulate gene expression in adult mice.
• As RNAi degrades respiratory syncitial virus RNAs in culture (Bitko et al. 2001, BMC Microbiol. 1: 34), we investigated whether RNAi could be directed against a human pathogenic RNA expressed in a mouse, namely that of hepatitis C virus (HCV). Infection by HCV (an RNA virus that infects 1 in 40 people worldwide) is the most common reason for liver transplantation in the United States and Europe. We fused the NS5B region (non-structural protein 5B, viral-polymerase-encoding region) of this virus with luciferase RNA and monitored RNAi by co-transfection in vivo. An siRNA targeting the NS5B region reduced luciferase expression from the chimaeric HCV NS5B protein-luciferase fusion by 75% (±6.8%; 6 animals per group). This result suggests that it may be feasible to use RNAi as a therapy against other important human pathogens.[0338]
• Although our results show that siRNAs are functional in mice, delivery remains a major obstacle. Unlike siRNAs, functional small-hairpin RNAs (shRNAs) can be expressed in vivo from DNA templates using RNA polymerase III promoters (Paddison et al. 2002, Genes Dev. 16: 948-958; Tuschl 2002, Nature Biotechnol. 20: 446-448); they are as effective as siRNAs in inducing gene suppression. Expression of a cognate shRNA (pShh1-Ff1) inhibited luciferase expression by up to 98% (±0.6%), with an average suppression of 92.8% (±3.39%) in three independent experiments (see FIGS. 54[0339]a,54b). An empty shRNA-expression vector had no effect; reversing the orientation of the shRNA (pShh1-Ff1rev) insert prevents gene silencing because it alters the termination by RNA polymerase III and generates an improperly structured shRNA. These findings indicate that plasmid-encoded shRNAs can induce a potent and specific RNAi response in adult mice.
• RNAi may find application in functional genomics or in identifying targets for designer drugs. It is a more promising system than gene-knockout mice because groups of genes can be simultaneously rendered ineffective without the need for time-consuming crosses. Gene therapy currently depends on the ectopic expression of exogenous proteins; however, RNAi may eventually complement this gain-of-function approach by silencing disease-related genes with DNA constructs that direct the expression of shRNAs. Our method of RNAi delivery could also be tailored to take advantage of developing viral and non-viral gene-transfer vectors in a clinical context.[0340]
EXAMPLE 11Germline Transmission of RNAi in Mice
• MicroRNA molecules (miRNAs) are small, noncoding RNA molecules that have been found in a diverse array of eukaryotes, including mammals. miRNA precursors share a characteristic secondary structure, forming short ‘hairpin’ RNAs. Genetic and biochemical studies have indicated that miRNAs are processed to their mature forms by Dicer, an RNAse III family nuclease, and function through RNA-mediated interference (RNAi) and related pathways to regulate the expression of target genes (Hannon 2002, Nature 418: 244-251; Pasquinelli et al. 2002, Annu. Rev. Cell. Dev. Biol. 18: 495-513). Recently, we and others have remodeled miRNAs to permit experimental manipulation of gene expression in mammalian cells and have dubbed these synthetic silencing triggers ‘short hairpin RNAs’ (shRNAs) (Paddison et al. 2002, Cancer Cell 2: 17-23). Silencing by shRNAs requires the RNAi machinery and correlates with the production of small interfering RNAs (siRNAs), which are a signature of RNAi.[0341]
• Expression of shRNAs can elicit either transient or stable silencing, depending upon whether the expression cassette is integrated into the genome of the recipient cultured cell (Paddison et al. 2002, Cancer Cell 2: 17-23). shRNA expression vectors also induce gene silencing in adult mice following transient delivery (Lewis et al. 2002, Nat. Genet. 32: 107-108; McCaffrey et al. 2002, Nature 418: 38-39). However, for shRNAs to be a viable genetic tool in mice, stable manipulation of gene expression is essential. Hemann and colleagues have demonstrated long-term suppression of gene expression in vivo following retroviral delivery of shRNA-expression cassettes to hematopoietic stem cells (Hemann et al. 2003, Nat. Genet. in the press). Here we sought to test whether shRNA-expression cassettes that were passed through the mouse germline could enforce heritable gene silencing.[0342]
• We began by taking standard transgenesis approaches (Gordon et al. 1993, Methods Enzymol. 225: 747-771) using shRNAs directed against a variety of targets with expected phenotypes, including the genes encoding tyrosinase (albino), myosin VIIa (shaker), Bmp-5 (crinkled ears), Hox a-10 (limb defects),[0343]homogentisate 1,2,-dioxygenase (urine turns black upon exposure to air), Hairless (hair loss) andmelanocortin 1 receptor (yellow). Three constructs per gene were linearized and injected into pronuclei to produce transgenic founder animals. Although we noted the presence of the transgene in some animals, virtually none showed a distinct or reproducible phenotype that was expected for a hypomorphic allele of the targeted gene.
• Therefore, we decided to take another approach: verifying the presence of the shRNA and its activity toward a target gene in cultured embryonic stem (ES) cells and then asking whether those cells retained suppression in a chimeric animal in vivo. We also planned to test whether such cells could pass a functional RNAi-inducing construct through the mouse germline. For these studies, we chose to examine a novel gene, Neil1, which is proposed to have a role in DNA repair. Oxidative damage accounts for 10,000 DNA lesions per cell per day in humans and is thought to contribute to carcinogenesis, aging and tissue damage following ischemia (Ames et al. 1993, Proc. Natl. Acad. Sci. USA 90: 7915-7922; Jackson et al. 2001, Mutat. Res. 477: 7-21). Oxidative DNA damage includes abasic sites, strand breaks and at least 20 oxidized bases, many of which are cytotoxic or pro-mutagenic (Dizdaroglu et al. 2002, Free Radic. Biol. Med. 32: 1102-1115). DNA N-glycosylases initiate the base excision repair pathway by recognizing specific bases in DNA and cleaving the sugar base bond to release the damaged base (David et al. 1998, Chem. Rev. 98: 1221-1262).[0344]
• The Neil genes are a newly discovered family of mammalian DNA N-glycosylases related to the Fpg/Nei family of proteins from[0345]Escherichia coli(Hazra et al. 2002, Proc. Natl. Acad. Sci. USA 99: 3523-3528; Bandaru et al. 2002, DNA Repair 1: 517-529). Neil1 recognizes and removes a wide spectrum of oxidized pyrimidines and ring-opened purines from DNA, including thymine glycol (Tg), 2,6-diamino-4-hydroxy-5-formamidopyrimidine (FapyG) and 4,6-diamino-5-formidopyrimidine (FapyA). Tg, FapyG and FapyA are among the most prevalent oxidized bases produced by ionizing radiation (Dizdaroglu et al. 2002, Free Radic. Biol. Med. 32: 1102-1115) and can block replicative DNA polymerases, which can, in turn, cause cell death (Asagoshi et al. 2002, J. Biol. Chem. 277: 14589-14597; Clark et al. 1989, Biochemistry 28: 775-779).
• The Nth1 and Ogg1 glycosylases each remove subsets of oxidized DNA bases that overlap with substrates of Neil1 (Nishimura 2002, Free Radic. Biol. Med. 32: 813-821; Asagoshi et al. 2000, Biochemistry 39: 11389-11398; Dizdaroglu et al. 1999, Biochemistry 38: 243-246). However, mice with null mutations in either Nth1 (Ocampo et al. 2002, Mol. Cell. Biol. 22: 6111-6121; Takao et al. 2002, EMBO J. 21: 3486-3493) or Ogg1 (Klungland et al. 1999, Proc. Natl. Acad. Sci. USA 96: 13300-13305; Minowa et al. 2000, Proc. Natl. Acad. Sci. USA 97: 4156-4161) are viable, raising the possibility that Neil1 activity tempers the loss of Nth1 or Ogg1. Recently, a residual Tg-DNA glycosylase activity in Nth1[0346]^−/− mice has been identified as Neil1 (Takao et al. 2002, J. Biol. Chem. 277: 42205-42213).
• We constructed a single shRNA expression vector targeting a sequence near the 5′ end of the Neil1 coding region. This vector was introduced into mouse embryonic stem cells by electroporation, and individual stable integrants were tested for expression of the Neil1 protein (see the weblink: http://www.cshl.edu/public/SCIENCE/hannon.html for detailed procedures). The majority of cell lines showed an ˜80% reduction in Neil1 protein, which correlated with a similar change in levels of Neil1 mRNA. These cells showed an approximately two-fold increase in their sensitivity to ionizing radiation, consistent with a role for Neil1 in DNA repair. Two independent ES cell lines were injected into BL/6 blastocysts, and several high-percentage chimeras were obtained. These chimeras were out-crossed, and germline transmission of the shRNA-expression construct was noted in numerous F[0347]₁progeny (13/27 for one line and 12/26 for the other).
• To determine whether the silencing of Neil1 that had been observed in ES cells was transmitted faithfully, we examined Neil1 mRNA and protein levels. Both were reduced by approximately the same extent that had been observed in the engineered ES cells (FIGS. 55, 56). Consistent with this having occurred through the RNAi pathway, we detected the presence of siRNAs corresponding to the shRNA sequence in F[0348]₁animals that carry the shRNA expression vector but not in those that lack the vector (FIG. 56b).
• The aforementioned data demonstrate that shRNAs can be used to create germline transgenic mice in which RNAi has silenced a target gene. These observations open the door to using of RNAi as a complement to standard knock-out methodologies and provide a means to rapidly assess the consequences of suppressing a gene of interest in a living animal. Coupled with activator-dependent U6 promoters, the use of shRNAs will ultimately provide methods for tissue-specific, inducible and reversible suppression of gene expression in mice.[0349]
• V. Equivalents[0350]
• Those skilled in the art will recognize, or be able to ascertain using no more than routine experimentation, many equivalents to the specific embodiments of the invention described herein. Such equivalents are intended to be encompassed by the following claims.[0351]
• All of the above-cited references and publications are hereby incorporated by reference.[0352]
• 14515775DNAHomo sapiensCDS(1)..(5775) 1 atg aaa agc cct gct ttg caa ccc ctc agc atg gca ggc ctg cag ctc 48 Met Lys Ser Pro Ala Leu Gln Pro Leu Ser Met Ala Gly Leu Gln Leu 1 5 10 15 atg acc cct gct tcc tca cca atg ggt cct ttc ttt gga ctg cca tgg 96 Met Thr Pro Ala Ser Ser Pro Met Gly Pro Phe Phe Gly Leu Pro Trp 20 25 30 caa caa gaa gca att cat gat aac att tat acg cca aga aaa tat cag 144 Gln Gln Glu Ala Ile His Asp Asn Ile Tyr Thr Pro Arg Lys Tyr Gln 35 40 45 gtt gaa ctg ctt gaa gca gct ctg gat cat aat acc atc gtc tgt tta 192 Val Glu Leu Leu Glu Ala Ala Leu Asp His Asn Thr Ile Val Cys Leu 50 55 60 aac act ggc tca ggg aag aca ttt att gct agt act act cta cta aag 240 Asn Thr Gly Ser Gly Lys Thr Phe Ile Ala Ser Thr Thr Leu Leu Lys 65 70 75 80 agc tgt ctc tat cta gat cta ggg gag act tca gct aga aat gga aaa 288 Ser Cys Leu Tyr Leu Asp Leu Gly Glu Thr Ser Ala Arg Asn Gly Lys 85 90 95 agg acg gtg ttc ttg gtc aac tct gca aac cag gtt gct caa caa gtg 336 Arg Thr Val Phe Leu Val Asn Ser Ala Asn Gln Val Ala Gln Gln Val 100 105 110 tca gct gtc aga act cat tca gat ctc aag gtt ggg gaa tac tca aac 384 Ser Ala Val Arg Thr His Ser Asp Leu Lys Val Gly Glu Tyr Ser Asn 115 120 125 cta gaa gta aat gca tct tgg aca aaa gag aga tgg aac caa gag ttt 432 Leu Glu Val Asn Ala Ser Trp Thr Lys Glu Arg Trp Asn Gln Glu Phe 130 135 140 act aag cac cag gtt ctc att atg act tgc tat gtc gcc ttg aat gtt 480 Thr Lys His Gln Val Leu Ile Met Thr Cys Tyr Val Ala Leu Asn Val 145 150 155 160 ttg aaa aat ggt tac tta tca ctg tca gac att aac ctt ttg gtg ttt 528 Leu Lys Asn Gly Tyr Leu Ser Leu Ser Asp Ile Asn Leu Leu Val Phe 165 170 175 gat gag tgt cat ctt gca atc cta gac cac ccc tat cga gaa ttt atg 576 Asp Glu Cys His Leu Ala Ile Leu Asp His Pro Tyr Arg Glu Phe Met 180 185 190 aag ctc tgt gaa att tgt cca tca tgt cct cgc att ttg gga cta act 624 Lys Leu Cys Glu Ile Cys Pro Ser Cys Pro Arg Ile Leu Gly Leu Thr 195 200 205 gct tcc att tta aat ggg aaa tgg gat cca gag gat ttg gaa gaa aag 672 Ala Ser Ile Leu Asn Gly Lys Trp Asp Pro Glu Asp Leu Glu Glu Lys 210 215 220 ttt cag aaa cta gag aaa att ctt aag agt aat gct gaa act gca act 720 Phe Gln Lys Leu Glu Lys Ile Leu Lys Ser Asn Ala Glu Thr Ala Thr 225 230 235 240 gac ctg gtg gtc tta gac agg tat act tct cag cca tgt gag att gtg 768 Asp Leu Val Val Leu Asp Arg Tyr Thr Ser Gln Pro Cys Glu Ile Val 245 250 255 gtg gat tgt gga cca ttt act gac aga agt ggg ctt tat gaa aga ctg 816 Val Asp Cys Gly Pro Phe Thr Asp Arg Ser Gly Leu Tyr Glu Arg Leu 260 265 270 ctg atg gaa tta gaa gaa gca ctt aat ttt atc aat gat tgt aat ata 864 Leu Met Glu Leu Glu Glu Ala Leu Asn Phe Ile Asn Asp Cys Asn Ile 275 280 285 tct gta cat tca aaa gaa aga gat tct act tta att tcg aaa cag ata 912 Ser Val His Ser Lys Glu Arg Asp Ser Thr Leu Ile Ser Lys Gln Ile 290 295 300 cta tca gac tgt cgt gcc gta ttg gta gtt ctg gga ccc tgg tgt gca 960 Leu Ser Asp Cys Arg Ala Val Leu Val Val Leu Gly Pro Trp Cys Ala 305 310 315 320 gat aaa gta gct gga atg atg gta aga gaa cta cag aaa tac atc aaa 1008 Asp Lys Val Ala Gly Met Met Val Arg Glu Leu Gln Lys Tyr Ile Lys 325 330 335 cat gag caa gag gag ctg cac agg aaa ttt tta ttg ttt aca gac act 1056 His Glu Gln Glu Glu Leu His Arg Lys Phe Leu Leu Phe Thr Asp Thr 340 345 350 ttc cta agg aaa ata cat gca cta tgt gaa gag cac ttc tca cct gcc 1104 Phe Leu Arg Lys Ile His Ala Leu Cys Glu Glu His Phe Ser Pro Ala 355 360 365 tca ctt gac ctg aaa ttt gta act cct aaa gta atc aaa ctg ctc gaa 1152 Ser Leu Asp Leu Lys Phe Val Thr Pro Lys Val Ile Lys Leu Leu Glu 370 375 380 atc tta cgc aaa tat aaa cca tat gag cga cac agt ttt gaa agc gtt 1200 Ile Leu Arg Lys Tyr Lys Pro Tyr Glu Arg His Ser Phe Glu Ser Val 385 390 395 400 gag tgg tat aat aat aga aat cag gat aat tat gtg tca tgg agt gat 1248 Glu Trp Tyr Asn Asn Arg Asn Gln Asp Asn Tyr Val Ser Trp Ser Asp 405 410 415 tct gag gat gat gat gag gat gaa gaa att gaa gaa aaa gag aag cca 1296 Ser Glu Asp Asp Asp Glu Asp Glu Glu Ile Glu Glu Lys Glu Lys Pro 420 425 430 gag aca aat ttt cct tct cct ttt acc aac att ttg tgc gga att att 1344 Glu Thr Asn Phe Pro Ser Pro Phe Thr Asn Ile Leu Cys Gly Ile Ile 435 440 445 ttt gtg gaa aga aga tac aca gca gtt gtc tta aac aga ttg ata aag 1392 Phe Val Glu Arg Arg Tyr Thr Ala Val Val Leu Asn Arg Leu Ile Lys 450 455 460 gaa gct ggc aaa caa gat cca gag ctg gct tat atc agt agc aat ttc 1440 Glu Ala Gly Lys Gln Asp Pro Glu Leu Ala Tyr Ile Ser Ser Asn Phe 465 470 475 480 ata act gga cat ggc att ggg aag aat cag cct cgc aac aac acg atg 1488 Ile Thr Gly His Gly Ile Gly Lys Asn Gln Pro Arg Asn Asn Thr Met 485 490 495 gaa gca gaa ttc aga aaa cag gaa gag gta ctt agg aaa ttt cga gca 1536 Glu Ala Glu Phe Arg Lys Gln Glu Glu Val Leu Arg Lys Phe Arg Ala 500 505 510 cat gag acc aac ctg ctt att gca aca agt att gta gaa gag ggt gtt 1584 His Glu Thr Asn Leu Leu Ile Ala Thr Ser Ile Val Glu Glu Gly Val 515 520 525 gat ata cca aaa tgc aac ttg gtg gtt cgt ttt gat ttg ccc aca gaa 1632 Asp Ile Pro Lys Cys Asn Leu Val Val Arg Phe Asp Leu Pro Thr Glu 530 535 540 tat cga tcc tat gtt caa tct aaa gga aga gca agg gca ccc atc tct 1680 Tyr Arg Ser Tyr Val Gln Ser Lys Gly Arg Ala Arg Ala Pro Ile Ser 545 550 555 560 aat tat ata atg tta gcg gat aca gac aaa ata aaa agt ttt gaa gaa 1728 Asn Tyr Ile Met Leu Ala Asp Thr Asp Lys Ile Lys Ser Phe Glu Glu 565 570 575 gac ctt aaa acc tac aaa gct att gaa aag atc ttg aga aac aag tgt 1776 Asp Leu Lys Thr Tyr Lys Ala Ile Glu Lys Ile Leu Arg Asn Lys Cys 580 585 590 tcc aag tcg gtt gat act ggt gag act gac att gat cct gtc atg gat 1824 Ser Lys Ser Val Asp Thr Gly Glu Thr Asp Ile Asp Pro Val Met Asp 595 600 605 gat gat cac gtt ttc cca cca tat gtg ttg agg cct gac gat ggt ggt 1872 Asp Asp His Val Phe Pro Pro Tyr Val Leu Arg Pro Asp Asp Gly Gly 610 615 620 cca cga gtc aca atc aac acg gcc att gga cac atc aat aga tac tgt 1920 Pro Arg Val Thr Ile Asn Thr Ala Ile Gly His Ile Asn Arg Tyr Cys 625 630 635 640 gct aga tta cca agt gat ccg ttt act cat cta gct cct aaa tgc aga 1968 Ala Arg Leu Pro Ser Asp Pro Phe Thr His Leu Ala Pro Lys Cys Arg 645 650 655 acc cga gag ttg cct gat ggt aca ttt tat tca act ctt tat ctg cca 2016 Thr Arg Glu Leu Pro Asp Gly Thr Phe Tyr Ser Thr Leu Tyr Leu Pro 660 665 670 att aac tca cct ctt cga gcc tcc att gtt ggt cca cca atg agc tgt 2064 Ile Asn Ser Pro Leu Arg Ala Ser Ile Val Gly Pro Pro Met Ser Cys 675 680 685 gta cga ttg gct gaa aga gtt gtc gct ctc att tgc tgt gag aaa ctg 2112 Val Arg Leu Ala Glu Arg Val Val Ala Leu Ile Cys Cys Glu Lys Leu 690 695 700 cac aaa att ggc gaa ctg gat gac cat ttg atg cca gtt ggg aaa gag 2160 His Lys Ile Gly Glu Leu Asp Asp His Leu Met Pro Val Gly Lys Glu 705 710 715 720 act gtt aaa tat gaa gag gag ctt gat ttg cat gat gaa gaa gag acc 2208 Thr Val Lys Tyr Glu Glu Glu Leu Asp Leu His Asp Glu Glu Glu Thr 725 730 735 agt gtt cca gga aga cca ggt tcc acg aaa cga agg cag tgc tac cca 2256 Ser Val Pro Gly Arg Pro Gly Ser Thr Lys Arg Arg Gln Cys Tyr Pro 740 745 750 aaa gca att cca gag tgt ttg agg gat agt tat ccc aga cct gat cag 2304 Lys Ala Ile Pro Glu Cys Leu Arg Asp Ser Tyr Pro Arg Pro Asp Gln 755 760 765 ccc tgt tac ctg tat gtg ata gga atg gtt tta act aca cct tta cct 2352 Pro Cys Tyr Leu Tyr Val Ile Gly Met Val Leu Thr Thr Pro Leu Pro 770 775 780 gat gaa ctc aac ttt aga agg cgg aag ctc tat cct cct gaa gat acc 2400 Asp Glu Leu Asn Phe Arg Arg Arg Lys Leu Tyr Pro Pro Glu Asp Thr 785 790 795 800 aca aga tgc ttt gga ata ctg acg gcc aaa ccc ata cct cag att cca 2448 Thr Arg Cys Phe Gly Ile Leu Thr Ala Lys Pro Ile Pro Gln Ile Pro 805 810 815 cac ttt cct gtg tac aca cgc tct gga gag gtt acc ata tcc att gag 2496 His Phe Pro Val Tyr Thr Arg Ser Gly Glu Val Thr Ile Ser Ile Glu 820 825 830 ttg aag aag tct ggt ttc atg ttg tct cta caa atg ctt gag ttg att 2544 Leu Lys Lys Ser Gly Phe Met Leu Ser Leu Gln Met Leu Glu Leu Ile 835 840 845 aca aga ctt cac cag tat ata ttc tca cat att ctt cgg ctt gaa aaa 2592 Thr Arg Leu His Gln Tyr Ile Phe Ser His Ile Leu Arg Leu Glu Lys 850 855 860 cct gca cta gaa ttt aaa cct aca gac gct gat tca gca tac tgt gtt 2640 Pro Ala Leu Glu Phe Lys Pro Thr Asp Ala Asp Ser Ala Tyr Cys Val 865 870 875 880 cta cct ctt aat gtt gtt aat gac tcc agc act ttg gat att gac ttt 2688 Leu Pro Leu Asn Val Val Asn Asp Ser Ser Thr Leu Asp Ile Asp Phe 885 890 895 aaa ttc atg gaa gat att gag aag tct gaa gct cgc ata ggc att ccc 2736 Lys Phe Met Glu Asp Ile Glu Lys Ser Glu Ala Arg Ile Gly Ile Pro 900 905 910 agt aca aag tat aca aaa gaa aca ccc ttt gtt ttt aaa tta gaa gat 2784 Ser Thr Lys Tyr Thr Lys Glu Thr Pro Phe Val Phe Lys Leu Glu Asp 915 920 925 tac caa gat gcc gtt atc att cca aga tat cgc aat ttt gat cag cct 2832 Tyr Gln Asp Ala Val Ile Ile Pro Arg Tyr Arg Asn Phe Asp Gln Pro 930 935 940 cat cga ttt tat gta gct gat gtg tac act gat ctt acc cca ctc agt 2880 His Arg Phe Tyr Val Ala Asp Val Tyr Thr Asp Leu Thr Pro Leu Ser 945 950 955 960 aaa ttt cct tcc cct gag tat gaa act ttt gca gaa tat tat aaa aca 2928 Lys Phe Pro Ser Pro Glu Tyr Glu Thr Phe Ala Glu Tyr Tyr Lys Thr 965 970 975 aag tac aac ctt gac cta acc aat ctc aac cag cca ctg ctg gat gtg 2976 Lys Tyr Asn Leu Asp Leu Thr Asn Leu Asn Gln Pro Leu Leu Asp Val 980 985 990 gac cac aca tct tca aga ctt aat ctt ttg aca cct cga cat ttg aat 3024 Asp His Thr Ser Ser Arg Leu Asn Leu Leu Thr Pro Arg His Leu Asn 995 1000 1005 cag aag ggg aaa gcg ctt cct tta agc agt gct gag aag agg aaa 3069 Gln Lys Gly Lys Ala Leu Pro Leu Ser Ser Ala Glu Lys Arg Lys 1010 1015 1020 gcc aaa tgg gaa agt ctg cag aat aaa cag ata ctg gtt cca gaa 3114 Ala Lys Trp Glu Ser Leu Gln Asn Lys Gln Ile Leu Val Pro Glu 1025 1030 1035 ctc tgt gct ata cat cca att cca gca tca ctg tgg aga aaa gct 3159 Leu Cys Ala Ile His Pro Ile Pro Ala Ser Leu Trp Arg Lys Ala 1040 1045 1050 gtt tgt ctc ccc agc ata ctt tat cgc ctt cac tgc ctt ttg act 3204 Val Cys Leu Pro Ser Ile Leu Tyr Arg Leu His Cys Leu Leu Thr 1055 1060 1065 gca gag gag cta aga gcc cag act gcc agc gat gct ggc gtg gga 3249 Ala Glu Glu Leu Arg Ala Gln Thr Ala Ser Asp Ala Gly Val Gly 1070 1075 1080 gtc aga tca ctt cct gcg gat ttt aga tac cct aac tta gac ttc 3294 Val Arg Ser Leu Pro Ala Asp Phe Arg Tyr Pro Asn Leu Asp Phe 1085 1090 1095 ggg tgg aaa aaa tct att gac agc aaa tct ttc atc tca att tct 3339 Gly Trp Lys Lys Ser Ile Asp Ser Lys Ser Phe Ile Ser Ile Ser 1100 1105 1110 aac tcc tct tca gct gaa aat gat aat tac tgt aag cac agc aca 3384 Asn Ser Ser Ser Ala Glu Asn Asp Asn Tyr Cys Lys His Ser Thr 1115 1120 1125 att gtc cct gaa aat gct gca cat caa ggt gct aat aga acc tcc 3429 Ile Val Pro Glu Asn Ala Ala His Gln Gly Ala Asn Arg Thr Ser 1130 1135 1140 tct cta gaa aat cat gac caa atg tct gtg aac tgc aga acg ttg 3474 Ser Leu Glu Asn His Asp Gln Met Ser Val Asn Cys Arg Thr Leu 1145 1150 1155 ctc agc gag tcc cct ggt aag ctc cac gtt gaa gtt tca gca gat 3519 Leu Ser Glu Ser Pro Gly Lys Leu His Val Glu Val Ser Ala Asp 1160 1165 1170 ctt aca gca att aat ggt ctt tct tac aat caa aat ctc gcc aat 3564 Leu Thr Ala Ile Asn Gly Leu Ser Tyr Asn Gln Asn Leu Ala Asn 1175 1180 1185 ggc agt tat gat tta gct aac aga gac ttt tgc caa gga aat cag 3609 Gly Ser Tyr Asp Leu Ala Asn Arg Asp Phe Cys Gln Gly Asn Gln 1190 1195 1200 cta aat tac tac aag cag gaa ata ccc gtg caa cca act acc tca 3654 Leu Asn Tyr Tyr Lys Gln Glu Ile Pro Val Gln Pro Thr Thr Ser 1205 1210 1215 tat tcc att cag aat tta tac agt tac gag aac cag ccc cag ccc 3699 Tyr Ser Ile Gln Asn Leu Tyr Ser Tyr Glu Asn Gln Pro Gln Pro 1220 1225 1230 agc gat gaa tgt act ctc ctg agt aat aaa tac ctt gat gga aat 3744 Ser Asp Glu Cys Thr Leu Leu Ser Asn Lys Tyr Leu Asp Gly Asn 1235 1240 1245 gct aac aaa tct acc tca gat gga agt cct gtg atg gcc gta atg 3789 Ala Asn Lys Ser Thr Ser Asp Gly Ser Pro Val Met Ala Val Met 1250 1255 1260 cct ggt acg aca gac act att caa gtg ctc aag ggc agg atg gat 3834 Pro Gly Thr Thr Asp Thr Ile Gln Val Leu Lys Gly Arg Met Asp 1265 1270 1275 tct gag cag agc cct tct att ggg tac tcc tca agg act ctt ggc 3879 Ser Glu Gln Ser Pro Ser Ile Gly Tyr Ser Ser Arg Thr Leu Gly 1280 1285 1290 ccc aat cct gga ctt att ctt cag gct ttg act ctg tca aac gct 3924 Pro Asn Pro Gly Leu Ile Leu Gln Ala Leu Thr Leu Ser Asn Ala 1295 1300 1305 agt gat gga ttt aac ctg gag cgg ctt gaa atg ctt ggc gac tcc 3969 Ser Asp Gly Phe Asn Leu Glu Arg Leu Glu Met Leu Gly Asp Ser 1310 1315 1320 ttt tta aag cat gcc atc acc aca tat cta ttt tgc act tac cct 4014 Phe Leu Lys His Ala Ile Thr Thr Tyr Leu Phe Cys Thr Tyr Pro 1325 1330 1335 gat gcg cat gag ggc cgc ctt tca tat atg aga agc aaa aag gtc 4059 Asp Ala His Glu Gly Arg Leu Ser Tyr Met Arg Ser Lys Lys Val 1340 1345 1350 agc aac tgt aat ctg tat cgc ctt gga aaa aag aag gga cta ccc 4104 Ser Asn Cys Asn Leu Tyr Arg Leu Gly Lys Lys Lys Gly Leu Pro 1355 1360 1365 agc cgc atg gtg gtg tca ata ttt gat ccc cct gtg aat tgg ctt 4149 Ser Arg Met Val Val Ser Ile Phe Asp Pro Pro Val Asn Trp Leu 1370 1375 1380 cct cct ggt tat gta gta aat caa gac aaa agc aac aca gat aaa 4194 Pro Pro Gly Tyr Val Val Asn Gln Asp Lys Ser Asn Thr Asp Lys 1385 1390 1395 tgg gaa aaa gat gaa atg aca aaa gac tgc atg ctg gcg aat ggc 4239 Trp Glu Lys Asp Glu Met Thr Lys Asp Cys Met Leu Ala Asn Gly 1400 1405 1410 aaa ctg gat gag gat tac gag gag gag gat gag gag gag gag agc 4284 Lys Leu Asp Glu Asp Tyr Glu Glu Glu Asp Glu Glu Glu Glu Ser 1415 1420 1425 ctg atg tgg agg gct ccg aag gaa gag gct gac tat gaa gat gat 4329 Leu Met Trp Arg Ala Pro Lys Glu Glu Ala Asp Tyr Glu Asp Asp 1430 1435 1440 ttc ctg gag tat gat cag gaa cat atc aga ttt ata gat aat atg 4374 Phe Leu Glu Tyr Asp Gln Glu His Ile Arg Phe Ile Asp Asn Met 1445 1450 1455 tta atg ggg tca gga gct ttt gta aag aaa atc tct ctt tct cct 4419 Leu Met Gly Ser Gly Ala Phe Val Lys Lys Ile Ser Leu Ser Pro 1460 1465 1470 ttt tca acc act gat tct gca tat gaa tgg aaa atg ccc aaa aaa 4464 Phe Ser Thr Thr Asp Ser Ala Tyr Glu Trp Lys Met Pro Lys Lys 1475 1480 1485 tcc tcc tta ggt agt atg cca ttt tca tca gat ttt gag gat ttt 4509 Ser Ser Leu Gly Ser Met Pro Phe Ser Ser Asp Phe Glu Asp Phe 1490 1495 1500 gac tac agc tct tgg gat gca atg tgc tat ctg gat cct agc aaa 4554 Asp Tyr Ser Ser Trp Asp Ala Met Cys Tyr Leu Asp Pro Ser Lys 1505 1510 1515 gct gtt gaa gaa gat gac ttt gtg gtg ggg ttc tgg aat cca tca 4599 Ala Val Glu Glu Asp Asp Phe Val Val Gly Phe Trp Asn Pro Ser 1520 1525 1530 gaa gaa aac tgt ggt gtt gac acg gga aag cag tcc att tct tac 4644 Glu Glu Asn Cys Gly Val Asp Thr Gly Lys Gln Ser Ile Ser Tyr 1535 1540 1545 gac ttg cac act gag cag tgt att gct gac aaa agc ata gcg gac 4689 Asp Leu His Thr Glu Gln Cys Ile Ala Asp Lys Ser Ile Ala Asp 1550 1555 1560 tgt gtg gaa gcc ctg ctg ggc tgc tat tta acc agc tgt ggg gag 4734 Cys Val Glu Ala Leu Leu Gly Cys Tyr Leu Thr Ser Cys Gly Glu 1565 1570 1575 agg gct gct cag ctt ttc ctc tgt tca ctg ggg ctg aag gtg ctc 4779 Arg Ala Ala Gln Leu Phe Leu Cys Ser Leu Gly Leu Lys Val Leu 1580 1585 1590 ccg gta att aaa agg act gat cgg gaa aag gcc ctg tgc cct act 4824 Pro Val Ile Lys Arg Thr Asp Arg Glu Lys Ala Leu Cys Pro Thr 1595 1600 1605 cgg gag aat ttc aac agc caa caa aag aac ctt tca gtg agc tgt 4869 Arg Glu Asn Phe Asn Ser Gln Gln Lys Asn Leu Ser Val Ser Cys 1610 1615 1620 gct gct gct tct gtg gcc agt tca cgc tct tct gta ttg aaa gac 4914 Ala Ala Ala Ser Val Ala Ser Ser Arg Ser Ser Val Leu Lys Asp 1625 1630 1635 tcg gaa tat ggt tgt ttg aag att cca cca aga tgt atg ttt gat 4959 Ser Glu Tyr Gly Cys Leu Lys Ile Pro Pro Arg Cys Met Phe Asp 1640 1645 1650 cat cca gat gca gat aaa aca ctg aat cac ctt ata tcg ggg ttt 5004 His Pro Asp Ala Asp Lys Thr Leu Asn His Leu Ile Ser Gly Phe 1655 1660 1665 gaa aat ttt gaa aag aaa atc aac tac aga ttc aag aat aag gct 5049 Glu Asn Phe Glu Lys Lys Ile Asn Tyr Arg Phe Lys Asn Lys Ala 1670 1675 1680 tac ctt ctc cag gct ttt aca cat gcc tcc tac cac tac aat act 5094 Tyr Leu Leu Gln Ala Phe Thr His Ala Ser Tyr His Tyr Asn Thr 1685 1690 1695 atc act gat tgt tac cag cgc tta gaa ttc ctg gga gat gcg att 5139 Ile Thr Asp Cys Tyr Gln Arg Leu Glu Phe Leu Gly Asp Ala Ile 1700 1705 1710 ttg gac tac ctc ata acc aag cac ctt tat gaa gac ccg cgg cag 5184 Leu Asp Tyr Leu Ile Thr Lys His Leu Tyr Glu Asp Pro Arg Gln 1715 1720 1725 cac tcc ccg ggg gtc ctg aca gac ctg cgg tct gcc ctg gtc aac 5229 His Ser Pro Gly Val Leu Thr Asp Leu Arg Ser Ala Leu Val Asn 1730 1735 1740 aac acc atc ttt gca tcg ctg gct gta aag tac gac tac cac aag 5274 Asn Thr Ile Phe Ala Ser Leu Ala Val Lys Tyr Asp Tyr His Lys 1745 1750 1755 tac ttc aaa gct gtc tct cct gag ctc ttc cat gtc att gat gac 5319 Tyr Phe Lys Ala Val Ser Pro Glu Leu Phe His Val Ile Asp Asp 1760 1765 1770 ttt gtg cag ttt cag ctt gag aag aat gaa atg caa gga atg gat 5364 Phe Val Gln Phe Gln Leu Glu Lys Asn Glu Met Gln Gly Met Asp 1775 1780 1785 tct gag ctt agg aga tct gag gag gat gaa gag aaa gaa gag gat 5409 Ser Glu Leu Arg Arg Ser Glu Glu Asp Glu Glu Lys Glu Glu Asp 1790 1795 1800 att gaa gtt cca aag gcc atg ggg gat att ttt gag tcg ctt gct 5454 Ile Glu Val Pro Lys Ala Met Gly Asp Ile Phe Glu Ser Leu Ala 1805 1810 1815 ggt gcc att tac atg gat agt ggg atg tca ctg gag aca gtc tgg 5499 Gly Ala Ile Tyr Met Asp Ser Gly Met Ser Leu Glu Thr Val Trp 1820 1825 1830 cag gtg tac tat ccc atg atg cgg cca cta ata gaa aag ttt tct 5544 Gln Val Tyr Tyr Pro Met Met Arg Pro Leu Ile Glu Lys Phe Ser 1835 1840 1845 gca aat gta ccc cgt tcc cct gtg cga gaa ttg ctt gaa atg gaa 5589 Ala Asn Val Pro Arg Ser Pro Val Arg Glu Leu Leu Glu Met Glu 1850 1855 1860 cca gaa act gcc aaa ttt agc ccg gct gag aga act tac gac ggg 5634 Pro Glu Thr Ala Lys Phe Ser Pro Ala Glu Arg Thr Tyr Asp Gly 1865 1870 1875 aag gtc aga gtc act gtg gaa gta gta gga aag ggg aaa ttt aaa 5679 Lys Val Arg Val Thr Val Glu Val Val Gly Lys Gly Lys Phe Lys 1880 1885 1890 ggt gtt ggt cga agt tac agg att gcc aaa tct gca gca gca aga 5724 Gly Val Gly Arg Ser Tyr Arg Ile Ala Lys Ser Ala Ala Ala Arg 1895 1900 1905 aga gcc ctc cga agc ctc aaa gct aat caa cct cag gtt ccc aat 5769 Arg Ala Leu Arg Ser Leu Lys Ala Asn Gln Pro Gln Val Pro Asn 1910 1915 1920 agc tga 5775 Ser21924PRTHomo sapiens 2 Met Lys Ser Pro Ala Leu Gln Pro Leu Ser Met Ala Gly Leu Gln Leu 1 5 10 15 Met Thr Pro Ala Ser Ser Pro Met Gly Pro Phe Phe Gly Leu Pro Trp 20 25 30 Gln Gln Glu Ala Ile His Asp Asn Ile Tyr Thr Pro Arg Lys Tyr Gln 35 40 45 Val Glu Leu Leu Glu Ala Ala Leu Asp His Asn Thr Ile Val Cys Leu 50 55 60 Asn Thr Gly Ser Gly Lys Thr Phe Ile Ala Ser Thr Thr Leu Leu Lys 65 70 75 80 Ser Cys Leu Tyr Leu Asp Leu Gly Glu Thr Ser Ala Arg Asn Gly Lys 85 90 95 Arg Thr Val Phe Leu Val Asn Ser Ala Asn Gln Val Ala Gln Gln Val 100 105 110 Ser Ala Val Arg Thr His Ser Asp Leu Lys Val Gly Glu Tyr Ser Asn 115 120 125 Leu Glu Val Asn Ala Ser Trp Thr Lys Glu Arg Trp Asn Gln Glu Phe 130 135 140 Thr Lys His Gln Val Leu Ile Met Thr Cys Tyr Val Ala Leu Asn Val 145 150 155 160 Leu Lys Asn Gly Tyr Leu Ser Leu Ser Asp Ile Asn Leu Leu Val Phe 165 170 175 Asp Glu Cys His Leu Ala Ile Leu Asp His Pro Tyr Arg Glu Phe Met 180 185 190 Lys Leu Cys Glu Ile Cys Pro Ser Cys Pro Arg Ile Leu Gly Leu Thr 195 200 205 Ala Ser Ile Leu Asn Gly Lys Trp Asp Pro Glu Asp Leu Glu Glu Lys 210 215 220 Phe Gln Lys Leu Glu Lys Ile Leu Lys Ser Asn Ala Glu Thr Ala Thr 225 230 235 240 Asp Leu Val Val Leu Asp Arg Tyr Thr Ser Gln Pro Cys Glu Ile Val 245 250 255 Val Asp Cys Gly Pro Phe Thr Asp Arg Ser Gly Leu Tyr Glu Arg Leu 260 265 270 Leu Met Glu Leu Glu Glu Ala Leu Asn Phe Ile Asn Asp Cys Asn Ile 275 280 285 Ser Val His Ser Lys Glu Arg Asp Ser Thr Leu Ile Ser Lys Gln Ile 290 295 300 Leu Ser Asp Cys Arg Ala Val Leu Val Val Leu Gly Pro Trp Cys Ala 305 310 315 320 Asp Lys Val Ala Gly Met Met Val Arg Glu Leu Gln Lys Tyr Ile Lys 325 330 335 His Glu Gln Glu Glu Leu His Arg Lys Phe Leu Leu Phe Thr Asp Thr 340 345 350 Phe Leu Arg Lys Ile His Ala Leu Cys Glu Glu His Phe Ser Pro Ala 355 360 365 Ser Leu Asp Leu Lys Phe Val Thr Pro Lys Val Ile Lys Leu Leu Glu 370 375 380 Ile Leu Arg Lys Tyr Lys Pro Tyr Glu Arg His Ser Phe Glu Ser Val 385 390 395 400 Glu Trp Tyr Asn Asn Arg Asn Gln Asp Asn Tyr Val Ser Trp Ser Asp 405 410 415 Ser Glu Asp Asp Asp Glu Asp Glu Glu Ile Glu Glu Lys Glu Lys Pro 420 425 430 Glu Thr Asn Phe Pro Ser Pro Phe Thr Asn Ile Leu Cys Gly Ile Ile 435 440 445 Phe Val Glu Arg Arg Tyr Thr Ala Val Val Leu Asn Arg Leu Ile Lys 450 455 460 Glu Ala Gly Lys Gln Asp Pro Glu Leu Ala Tyr Ile Ser Ser Asn Phe 465 470 475 480 Ile Thr Gly His Gly Ile Gly Lys Asn Gln Pro Arg Asn Asn Thr Met 485 490 495 Glu Ala Glu Phe Arg Lys Gln Glu Glu Val Leu Arg Lys Phe Arg Ala 500 505 510 His Glu Thr Asn Leu Leu Ile Ala Thr Ser Ile Val Glu Glu Gly Val 515 520 525 Asp Ile Pro Lys Cys Asn Leu Val Val Arg Phe Asp Leu Pro Thr Glu 530 535 540 Tyr Arg Ser Tyr Val Gln Ser Lys Gly Arg Ala Arg Ala Pro Ile Ser 545 550 555 560 Asn Tyr Ile Met Leu Ala Asp Thr Asp Lys Ile Lys Ser Phe Glu Glu 565 570 575 Asp Leu Lys Thr Tyr Lys Ala Ile Glu Lys Ile Leu Arg Asn Lys Cys 580 585 590 Ser Lys Ser Val Asp Thr Gly Glu Thr Asp Ile Asp Pro Val Met Asp 595 600 605 Asp Asp His Val Phe Pro Pro Tyr Val Leu Arg Pro Asp Asp Gly Gly 610 615 620 Pro Arg Val Thr Ile Asn Thr Ala Ile Gly His Ile Asn Arg Tyr Cys 625 630 635 640 Ala Arg Leu Pro Ser Asp Pro Phe Thr His Leu Ala Pro Lys Cys Arg 645 650 655 Thr Arg Glu Leu Pro Asp Gly Thr Phe Tyr Ser Thr Leu Tyr Leu Pro 660 665 670 Ile Asn Ser Pro Leu Arg Ala Ser Ile Val Gly Pro Pro Met Ser Cys 675 680 685 Val Arg Leu Ala Glu Arg Val Val Ala Leu Ile Cys Cys Glu Lys Leu 690 695 700 His Lys Ile Gly Glu Leu Asp Asp His Leu Met Pro Val Gly Lys Glu 705 710 715 720 Thr Val Lys Tyr Glu Glu Glu Leu Asp Leu His Asp Glu Glu Glu Thr 725 730 735 Ser Val Pro Gly Arg Pro Gly Ser Thr Lys Arg Arg Gln Cys Tyr Pro 740 745 750 Lys Ala Ile Pro Glu Cys Leu Arg Asp Ser Tyr Pro Arg Pro Asp Gln 755 760 765 Pro Cys Tyr Leu Tyr Val Ile Gly Met Val Leu Thr Thr Pro Leu Pro 770 775 780 Asp Glu Leu Asn Phe Arg Arg Arg Lys Leu Tyr Pro Pro Glu Asp Thr 785 790 795 800 Thr Arg Cys Phe Gly Ile Leu Thr Ala Lys Pro Ile Pro Gln Ile Pro 805 810 815 His Phe Pro Val Tyr Thr Arg Ser Gly Glu Val Thr Ile Ser Ile Glu 820 825 830 Leu Lys Lys Ser Gly Phe Met Leu Ser Leu Gln Met Leu Glu Leu Ile 835 840 845 Thr Arg Leu His Gln Tyr Ile Phe Ser His Ile Leu Arg Leu Glu Lys 850 855 860 Pro Ala Leu Glu Phe Lys Pro Thr Asp Ala Asp Ser Ala Tyr Cys Val 865 870 875 880 Leu Pro Leu Asn Val Val Asn Asp Ser Ser Thr Leu Asp Ile Asp Phe 885 890 895 Lys Phe Met Glu Asp Ile Glu Lys Ser Glu Ala Arg Ile Gly Ile Pro 900 905 910 Ser Thr Lys Tyr Thr Lys Glu Thr Pro Phe Val Phe Lys Leu Glu Asp 915 920 925 Tyr Gln Asp Ala Val Ile Ile Pro Arg Tyr Arg Asn Phe Asp Gln Pro 930 935 940 His Arg Phe Tyr Val Ala Asp Val Tyr Thr Asp Leu Thr Pro Leu Ser 945 950 955 960 Lys Phe Pro Ser Pro Glu Tyr Glu Thr Phe Ala Glu Tyr Tyr Lys Thr 965 970 975 Lys Tyr Asn Leu Asp Leu Thr Asn Leu Asn Gln Pro Leu Leu Asp Val 980 985 990 Asp His Thr Ser Ser Arg Leu Asn Leu Leu Thr Pro Arg His Leu Asn 995 1000 1005 Gln Lys Gly Lys Ala Leu Pro Leu Ser Ser Ala Glu Lys Arg Lys 1010 1015 1020 Ala Lys Trp Glu Ser Leu Gln Asn Lys Gln Ile Leu Val Pro Glu 1025 1030 1035 Leu Cys Ala Ile His Pro Ile Pro Ala Ser Leu Trp Arg Lys Ala 1040 1045 1050 Val Cys Leu Pro Ser Ile Leu Tyr Arg Leu His Cys Leu Leu Thr 1055 1060 1065 Ala Glu Glu Leu Arg Ala Gln Thr Ala Ser Asp Ala Gly Val Gly 1070 1075 1080 Val Arg Ser Leu Pro Ala Asp Phe Arg Tyr Pro Asn Leu Asp Phe 1085 1090 1095 Gly Trp Lys Lys Ser Ile Asp Ser Lys Ser Phe Ile Ser Ile Ser 1100 1105 1110 Asn Ser Ser Ser Ala Glu Asn Asp Asn Tyr Cys Lys His Ser Thr 1115 1120 1125 Ile Val Pro Glu Asn Ala Ala His Gln Gly Ala Asn Arg Thr Ser 1130 1135 1140 Ser Leu Glu Asn His Asp Gln Met Ser Val Asn Cys Arg Thr Leu 1145 1150 1155 Leu Ser Glu Ser Pro Gly Lys Leu His Val Glu Val Ser Ala Asp 1160 1165 1170 Leu Thr Ala Ile Asn Gly Leu Ser Tyr Asn Gln Asn Leu Ala Asn 1175 1180 1185 Gly Ser Tyr Asp Leu Ala Asn Arg Asp Phe Cys Gln Gly Asn Gln 1190 1195 1200 Leu Asn Tyr Tyr Lys Gln Glu Ile Pro Val Gln Pro Thr Thr Ser 1205 1210 1215 Tyr Ser Ile Gln Asn Leu Tyr Ser Tyr Glu Asn Gln Pro Gln Pro 1220 1225 1230 Ser Asp Glu Cys Thr Leu Leu Ser Asn Lys Tyr Leu Asp Gly Asn 1235 1240 1245 Ala Asn Lys Ser Thr Ser Asp Gly Ser Pro Val Met Ala Val Met 1250 1255 1260 Pro Gly Thr Thr Asp Thr Ile Gln Val Leu Lys Gly Arg Met Asp 1265 1270 1275 Ser Glu Gln Ser Pro Ser Ile Gly Tyr Ser Ser Arg Thr Leu Gly 1280 1285 1290 Pro Asn Pro Gly Leu Ile Leu Gln Ala Leu Thr Leu Ser Asn Ala 1295 1300 1305 Ser Asp Gly Phe Asn Leu Glu Arg Leu Glu Met Leu Gly Asp Ser 1310 1315 1320 Phe Leu Lys His Ala Ile Thr Thr Tyr Leu Phe Cys Thr Tyr Pro 1325 1330 1335 Asp Ala His Glu Gly Arg Leu Ser Tyr Met Arg Ser Lys Lys Val 1340 1345 1350 Ser Asn Cys Asn Leu Tyr Arg Leu Gly Lys Lys Lys Gly Leu Pro 1355 1360 1365 Ser Arg Met Val Val Ser Ile Phe Asp Pro Pro Val Asn Trp Leu 1370 1375 1380 Pro Pro Gly Tyr Val Val Asn Gln Asp Lys Ser Asn Thr Asp Lys 1385 1390 1395 Trp Glu Lys Asp Glu Met Thr Lys Asp Cys Met Leu Ala Asn Gly 1400 1405 1410 Lys Leu Asp Glu Asp Tyr Glu Glu Glu Asp Glu Glu Glu Glu Ser 1415 1420 1425 Leu Met Trp Arg Ala Pro Lys Glu Glu Ala Asp Tyr Glu Asp Asp 1430 1435 1440 Phe Leu Glu Tyr Asp Gln Glu His Ile Arg Phe Ile Asp Asn Met 1445 1450 1455 Leu Met Gly Ser Gly Ala Phe Val Lys Lys Ile Ser Leu Ser Pro 1460 1465 1470 Phe Ser Thr Thr Asp Ser Ala Tyr Glu Trp Lys Met Pro Lys Lys 1475 1480 1485 Ser Ser Leu Gly Ser Met Pro Phe Ser Ser Asp Phe Glu Asp Phe 1490 1495 1500 Asp Tyr Ser Ser Trp Asp Ala Met Cys Tyr Leu Asp Pro Ser Lys 1505 1510 1515 Ala Val Glu Glu Asp Asp Phe Val Val Gly Phe Trp Asn Pro Ser 1520 1525 1530 Glu Glu Asn Cys Gly Val Asp Thr Gly Lys Gln Ser Ile Ser Tyr 1535 1540 1545 Asp Leu His Thr Glu Gln Cys Ile Ala Asp Lys Ser Ile Ala Asp 1550 1555 1560 Cys Val Glu Ala Leu Leu Gly Cys Tyr Leu Thr Ser Cys Gly Glu 1565 1570 1575 Arg Ala Ala Gln Leu Phe Leu Cys Ser Leu Gly Leu Lys Val Leu 1580 1585 1590 Pro Val Ile Lys Arg Thr Asp Arg Glu Lys Ala Leu Cys Pro Thr 1595 1600 1605 Arg Glu Asn Phe Asn Ser Gln Gln Lys Asn Leu Ser Val Ser Cys 1610 1615 1620 Ala Ala Ala Ser Val Ala Ser Ser Arg Ser Ser Val Leu Lys Asp 1625 1630 1635 Ser Glu Tyr Gly Cys Leu Lys Ile Pro Pro Arg Cys Met Phe Asp 1640 1645 1650 His Pro Asp Ala Asp Lys Thr Leu Asn His Leu Ile Ser Gly Phe 1655 1660 1665 Glu Asn Phe Glu Lys Lys Ile Asn Tyr Arg Phe Lys Asn Lys Ala 1670 1675 1680 Tyr Leu Leu Gln Ala Phe Thr His Ala Ser Tyr His Tyr Asn Thr 1685 1690 1695 Ile Thr Asp Cys Tyr Gln Arg Leu Glu Phe Leu Gly Asp Ala Ile 1700 1705 1710 Leu Asp Tyr Leu Ile Thr Lys His Leu Tyr Glu Asp Pro Arg Gln 1715 1720 1725 His Ser Pro Gly Val Leu Thr Asp Leu Arg Ser Ala Leu Val Asn 1730 1735 1740 Asn Thr Ile Phe Ala Ser Leu Ala Val Lys Tyr Asp Tyr His Lys 1745 1750 1755 Tyr Phe Lys Ala Val Ser Pro Glu Leu Phe His Val Ile Asp Asp 1760 1765 1770 Phe Val Gln Phe Gln Leu Glu Lys Asn Glu Met Gln Gly Met Asp 1775 1780 1785 Ser Glu Leu Arg Arg Ser Glu Glu Asp Glu Glu Lys Glu Glu Asp 1790 1795 1800 Ile Glu Val Pro Lys Ala Met Gly Asp Ile Phe Glu Ser Leu Ala 1805 1810 1815 Gly Ala Ile Tyr Met Asp Ser Gly Met Ser Leu Glu Thr Val Trp 1820 1825 1830 Gln Val Tyr Tyr Pro Met Met Arg Pro Leu Ile Glu Lys Phe Ser 1835 1840 1845 Ala Asn Val Pro Arg Ser Pro Val Arg Glu Leu Leu Glu Met Glu 1850 1855 1860 Pro Glu Thr Ala Lys Phe Ser Pro Ala Glu Arg Thr Tyr Asp Gly 1865 1870 1875 Lys Val Arg Val Thr Val Glu Val Val Gly Lys Gly Lys Phe Lys 1880 1885 1890 Gly Val Gly Arg Ser Tyr Arg Ile Ala Lys Ser Ala Ala Ala Arg 1895 1900 1905 Arg Ala Leu Arg Ser Leu Lys Ala Asn Gln Pro Gln Val Pro Asn 1910 1915 1920 Ser36750DNADrosophila melanogasterCDS(1)..(6750) 3 atg gcg ttc cac tgg tgc gac aac aat ctg cac acc acc gtg ttc acg 48 Met Ala Phe His Trp Cys Asp Asn Asn Leu His Thr Thr Val Phe Thr 1 5 10 15 ccg cgc gac ttt cag gtg gag cta ctg gcc acc gcc tac gag cgg aac 96 Pro Arg Asp Phe Gln Val Glu Leu Leu Ala Thr Ala Tyr Glu Arg Asn 20 25 30 acg att att tgc ctg ggc cat cga agt tcc aag gag ttt ata gcc ctc 144 Thr Ile Ile Cys Leu Gly His Arg Ser Ser Lys Glu Phe Ile Ala Leu 35 40 45 aag ctg ctc cag gag ctg tcg cgt cga gca cgc cga cat ggt cgt gtc 192 Lys Leu Leu Gln Glu Leu Ser Arg Arg Ala Arg Arg His Gly Arg Val 50 55 60 agt gtc tat ctc agt tgc gag gtt ggc acc agc acg gaa cca tgc tcc 240 Ser Val Tyr Leu Ser Cys Glu Val Gly Thr Ser Thr Glu Pro Cys Ser 65 70 75 80 atc tac acg atg ctc acc cac ttg act gac ctg cgg gtg tgg cag gag 288 Ile Tyr Thr Met Leu Thr His Leu Thr Asp Leu Arg Val Trp Gln Glu 85 90 95 cag ccg gat atg caa att ccc ttt gat cat tgc tgg acg gac tat cac 336 Gln Pro Asp Met Gln Ile Pro Phe Asp His Cys Trp Thr Asp Tyr His 100 105 110 gtt tcc atc cta cgg cca gag gga ttt ctt tat ctg ctc gaa act cgc 384 Val Ser Ile Leu Arg Pro Glu Gly Phe Leu Tyr Leu Leu Glu Thr Arg 115 120 125 gag ctg ctg ctg agc agc gtc gaa ctg atc gtg ctg gaa gat tgt cat 432 Glu Leu Leu Leu Ser Ser Val Glu Leu Ile Val Leu Glu Asp Cys His 130 135 140 gac agc gcc gtt tat cag agg ata agg cct ctg ttc gag aat cac att 480 Asp Ser Ala Val Tyr Gln Arg Ile Arg Pro Leu Phe Glu Asn His Ile 145 150 155 160 atg cca gcg cca ccg gcg gac agg cca cgg att ctc gga ctc gct gga 528 Met Pro Ala Pro Pro Ala Asp Arg Pro Arg Ile Leu Gly Leu Ala Gly 165 170 175 ccg ctg cac agc gcc gga tgt gag ctg cag caa ctg agc gcc atg ctg 576 Pro Leu His Ser Ala Gly Cys Glu Leu Gln Gln Leu Ser Ala Met Leu 180 185 190 gcc acc ctg gag cag agt gtg ctt tgc cag atc gag acg gcc agt gat 624 Ala Thr Leu Glu Gln Ser Val Leu Cys Gln Ile Glu Thr Ala Ser Asp 195 200 205 att gtc acc gtg ttg cgt tac tgt tcc cga ccg cac gaa tac atc gta 672 Ile Val Thr Val Leu Arg Tyr Cys Ser Arg Pro His Glu Tyr Ile Val 210 215 220 cag tgc gcc ccc ttc gag atg gac gaa ctg tcc ctg gtg ctt gcc gat 720 Gln Cys Ala Pro Phe Glu Met Asp Glu Leu Ser Leu Val Leu Ala Asp 225 230 235 240 gtg ctc aac aca cac aag tcc ttt tta ttg gac cac cgc tac gat ccc 768 Val Leu Asn Thr His Lys Ser Phe Leu Leu Asp His Arg Tyr Asp Pro 245 250 255 tac gaa atc tac ggc aca gac cag ttt atg gac gaa ctg aaa gac ata 816 Tyr Glu Ile Tyr Gly Thr Asp Gln Phe Met Asp Glu Leu Lys Asp Ile 260 265 270 ccc gat ccc aag gtg gac ccc ctg aac gtc atc aac tca cta ctg gtc 864 Pro Asp Pro Lys Val Asp Pro Leu Asn Val Ile Asn Ser Leu Leu Val 275 280 285 gtg ctg cac gag atg ggt cct tgg tgc acg cag cgg gct gca cat cac 912 Val Leu His Glu Met Gly Pro Trp Cys Thr Gln Arg Ala Ala His His 290 295 300 ttt tac caa tgc aat gag aag tta aag gtg aag acg ccg cac gaa cgt 960 Phe Tyr Gln Cys Asn Glu Lys Leu Lys Val Lys Thr Pro His Glu Arg 305 310 315 320 cac tac ttg ctg tac tgc cta gtg agc acg gcc ctt atc caa ctg tac 1008 His Tyr Leu Leu Tyr Cys Leu Val Ser Thr Ala Leu Ile Gln Leu Tyr 325 330 335 tcc ctc tgc gaa cac gca ttc cat cga cat tta gga agt ggc agc gat 1056 Ser Leu Cys Glu His Ala Phe His Arg His Leu Gly Ser Gly Ser Asp 340 345 350 tca cgc cag acc atc gaa cgc tat tcc agc ccc aag gtg cga cgt ctg 1104 Ser Arg Gln Thr Ile Glu Arg Tyr Ser Ser Pro Lys Val Arg Arg Leu 355 360 365 ttg cag aca ctg agg tgc ttc aag ccg gaa gag gtg cac acc caa gcg 1152 Leu Gln Thr Leu Arg Cys Phe Lys Pro Glu Glu Val His Thr Gln Ala 370 375 380 gac gga ctg cgc aga atg cgg cat cag gtg gat cag gcg gac ttc aat 1200 Asp Gly Leu Arg Arg Met Arg His Gln Val Asp Gln Ala Asp Phe Asn 385 390 395 400 cgg tta tct cat acg ctg gaa agc aag tgc cga atg gtg gat caa atg 1248 Arg Leu Ser His Thr Leu Glu Ser Lys Cys Arg Met Val Asp Gln Met 405 410 415 gac caa ccg ccg acg gag aca cga gcc ctg gtg gcc act ctt gag cag 1296 Asp Gln Pro Pro Thr Glu Thr Arg Ala Leu Val Ala Thr Leu Glu Gln 420 425 430 att ctg cac acg aca gag gac agg cag acg aac aga agc gcc gct cgg 1344 Ile Leu His Thr Thr Glu Asp Arg Gln Thr Asn Arg Ser Ala Ala Arg 435 440 445 gtg act cct act cct act ccc gct cat gcg aag ccg aaa cct agc tct 1392 Val Thr Pro Thr Pro Thr Pro Ala His Ala Lys Pro Lys Pro Ser Ser 450 455 460 ggt gcc aac act gca caa cca cga act cgt aga cgt gtg tac acc agg 1440 Gly Ala Asn Thr Ala Gln Pro Arg Thr Arg Arg Arg Val Tyr Thr Arg 465 470 475 480 cgc cac cac cgg gat cac aat gat ggc agc gac acg ctc tgc gca ctg 1488 Arg His His Arg Asp His Asn Asp Gly Ser Asp Thr Leu Cys Ala Leu 485 490 495 att tac tgc aac cag aac cac acg gct cgc gtg ctc ttt gag ctt cta 1536 Ile Tyr Cys Asn Gln Asn His Thr Ala Arg Val Leu Phe Glu Leu Leu 500 505 510 gcg gag att agc aga cgt gat ccc gat ctc aag ttc cta cgc tgc cag 1584 Ala Glu Ile Ser Arg Arg Asp Pro Asp Leu Lys Phe Leu Arg Cys Gln 515 520 525 tac acc acg gac cgg gtg gca gat ccc acc acg gag ccc aaa gag gct 1632 Tyr Thr Thr Asp Arg Val Ala Asp Pro Thr Thr Glu Pro Lys Glu Ala 530 535 540 gag ttg gag cac cgg cgg cag gaa gag gtg cta aag cgc ttc cgc atg 1680 Glu Leu Glu His Arg Arg Gln Glu Glu Val Leu Lys Arg Phe Arg Met 545 550 555 560 cat gac tgc aat gtc ctg atc ggt act tcg gtg ctg gaa gag ggc atc 1728 His Asp Cys Asn Val Leu Ile Gly Thr Ser Val Leu Glu Glu Gly Ile 565 570 575 gat gtg ccc aag tgc aat ttg gtt gtg cgc tgg gat ccg cca acc aca 1776 Asp Val Pro Lys Cys Asn Leu Val Val Arg Trp Asp Pro Pro Thr Thr 580 585 590 tat cgc agt tac gtt cag tgc aaa ggt cga gcc cgt gct gct cca gcc 1824 Tyr Arg Ser Tyr Val Gln Cys Lys Gly Arg Ala Arg Ala Ala Pro Ala 595 600 605 tat cat gtc att ctc gtc gct ccg agt tat aaa agc cca act gtg ggg 1872 Tyr His Val Ile Leu Val Ala Pro Ser Tyr Lys Ser Pro Thr Val Gly 610 615 620 tca gtg cag ctg acc gat cgg agt cat cgg tat att tgc gcg act ggt 1920 Ser Val Gln Leu Thr Asp Arg Ser His Arg Tyr Ile Cys Ala Thr Gly 625 630 635 640 gat act aca gag gcg gac agc gac tct gat gat tca gcg atg cca aac 1968 Asp Thr Thr Glu Ala Asp Ser Asp Ser Asp Asp Ser Ala Met Pro Asn 645 650 655 tcg tcc ggc tcg gat ccc tat act ttt ggc acg gca cgc gga acc gtg 2016 Ser Ser Gly Ser Asp Pro Tyr Thr Phe Gly Thr Ala Arg Gly Thr Val 660 665 670 aag atc ctc aac ccc gaa gtg ttc agt aaa caa cca ccg aca gcg tgc 2064 Lys Ile Leu Asn Pro Glu Val Phe Ser Lys Gln Pro Pro Thr Ala Cys 675 680 685 gac att aag ctg cag gag atc cag gac gaa ttg cca gcc gca gcg cag 2112 Asp Ile Lys Leu Gln Glu Ile Gln Asp Glu Leu Pro Ala Ala Ala Gln 690 695 700 ctg gat acg agc aac tcc agc gac gaa gcc gtc agc atg agt aac acg 2160 Leu Asp Thr Ser Asn Ser Ser Asp Glu Ala Val Ser Met Ser Asn Thr 705 710 715 720 tct cca agc gag agc agt aca gaa caa aaa tcc aga cgc ttc cag tgc 2208 Ser Pro Ser Glu Ser Ser Thr Glu Gln Lys Ser Arg Arg Phe Gln Cys 725 730 735 gag ctg agc tct tta acg gag cca gaa gac aca agt gat act aca gcc 2256 Glu Leu Ser Ser Leu Thr Glu Pro Glu Asp Thr Ser Asp Thr Thr Ala 740 745 750 gaa atc gat act gct cat agt tta gcc agc acc acg aag gac ttg gtg 2304 Glu Ile Asp Thr Ala His Ser Leu Ala Ser Thr Thr Lys Asp Leu Val 755 760 765 cat caa atg gca cag tat cgc gaa atc gag cag atg ctg cta tcc aag 2352 His Gln Met Ala Gln Tyr Arg Glu Ile Glu Gln Met Leu Leu Ser Lys 770 775 780 tgc gcc aac aca gag ccg ccg gag cag gag cag agt gag gcg gaa cgt 2400 Cys Ala Asn Thr Glu Pro Pro Glu Gln Glu Gln Ser Glu Ala Glu Arg 785 790 795 800 ttt agt gcc tgc ctg gcc gca tac cga ccc aag ccg cac ctg cta aca 2448 Phe Ser Ala Cys Leu Ala Ala Tyr Arg Pro Lys Pro His Leu Leu Thr 805 810 815 ggc gcc tcc gtg gat ctg ggt tct gct ata gct ttg gtc aac aag tac 2496 Gly Ala Ser Val Asp Leu Gly Ser Ala Ile Ala Leu Val Asn Lys Tyr 820 825 830 tgc gcc cga ctg cca agc gac acg ttc acc aag ttg acg gcg ttg tgg 2544 Cys Ala Arg Leu Pro Ser Asp Thr Phe Thr Lys Leu Thr Ala Leu Trp 835 840 845 cgc tgc acc cga aac gaa agg gct gga gtg acc ctg ttt cag tac aca 2592 Arg Cys Thr Arg Asn Glu Arg Ala Gly Val Thr Leu Phe Gln Tyr Thr 850 855 860 ctc cgt ctg ccc atc aac tcg cca ttg aag cat gac att gtg ggt ctt 2640 Leu Arg Leu Pro Ile Asn Ser Pro Leu Lys His Asp Ile Val Gly Leu 865 870 875 880 ccg atg cca act caa aca ttg gcc cgc cga ctg gct gcc ttg cag gct 2688 Pro Met Pro Thr Gln Thr Leu Ala Arg Arg Leu Ala Ala Leu Gln Ala 885 890 895 tgc gtg gaa ctg cac agg atc ggt gag tta gac gat cag ttg cag cct 2736 Cys Val Glu Leu His Arg Ile Gly Glu Leu Asp Asp Gln Leu Gln Pro 900 905 910 atc ggc aag gag gga ttt cgt gcc ctg gag ccg gac tgg gag tgc ttt 2784 Ile Gly Lys Glu Gly Phe Arg Ala Leu Glu Pro Asp Trp Glu Cys Phe 915 920 925 gaa ctg gag cca gag gac gaa cag att gtg cag cta agc gat gaa cca 2832 Glu Leu Glu Pro Glu Asp Glu Gln Ile Val Gln Leu Ser Asp Glu Pro 930 935 940 cgt ccg gga aca acg aag cgt cgt cag tac tat tac aaa cgc att gca 2880 Arg Pro Gly Thr Thr Lys Arg Arg Gln Tyr Tyr Tyr Lys Arg Ile Ala 945 950 955 960 tcc gaa ttt tgc gat tgc cgt ccc gtt gcc gga gcg cca tgc tat ttg 2928 Ser Glu Phe Cys Asp Cys Arg Pro Val Ala Gly Ala Pro Cys Tyr Leu 965 970 975 tac ttt atc caa ctg acg ctc caa tgt ccg att ccc gaa gag caa aac 2976 Tyr Phe Ile Gln Leu Thr Leu Gln Cys Pro Ile Pro Glu Glu Gln Asn 980 985 990 acg cgg gga cgc aag att tat ccg ccc gaa gat gcg cag cag gga ttc 3024 Thr Arg Gly Arg Lys Ile Tyr Pro Pro Glu Asp Ala Gln Gln Gly Phe 995 1000 1005 ggc att cta acc acc aaa cgg ata ccc aag ctg agt gct ttc tcg 3069 Gly Ile Leu Thr Thr Lys Arg Ile Pro Lys Leu Ser Ala Phe Ser 1010 1015 1020 ata ttc acg cgt tcc ggt gag gtg aag gtt tcc ctg gag tta gct 3114 Ile Phe Thr Arg Ser Gly Glu Val Lys Val Ser Leu Glu Leu Ala 1025 1030 1035 aag gaa cgc gtg att cta act agc gaa caa ata gtc tgc atc aac 3159 Lys Glu Arg Val Ile Leu Thr Ser Glu Gln Ile Val Cys Ile Asn 1040 1045 1050 gga ttt tta aac tac acg ttc acc aat gta ctg cgt ttg caa aag 3204 Gly Phe Leu Asn Tyr Thr Phe Thr Asn Val Leu Arg Leu Gln Lys 1055 1060 1065 ttt ctg atg ctc ttc gat ccg gac tcc acg gaa aat tgt gta ttc 3249 Phe Leu Met Leu Phe Asp Pro Asp Ser Thr Glu Asn Cys Val Phe 1070 1075 1080 att gtg ccc acc gtg aag gca cca gct ggc ggc aag cac atc gac 3294 Ile Val Pro Thr Val Lys Ala Pro Ala Gly Gly Lys His Ile Asp 1085 1090 1095 tgg cag ttt ctg gag ctg atc caa gcg aat gga aat aca atg cca 3339 Trp Gln Phe Leu Glu Leu Ile Gln Ala Asn Gly Asn Thr Met Pro 1100 1105 1110 cgg gca gtg ccc gat gag gag cgc cag gcg cag ccg ttt gat ccg 3384 Arg Ala Val Pro Asp Glu Glu Arg Gln Ala Gln Pro Phe Asp Pro 1115 1120 1125 caa cgc ttc cag gat gcc gtc gtt atg ccg tgg tat cgc aac cag 3429 Gln Arg Phe Gln Asp Ala Val Val Met Pro Trp Tyr Arg Asn Gln 1130 1135 1140 gat caa ccg cag tat ttc tat gtg gcg gag ata tgt cca cat cta 3474 Asp Gln Pro Gln Tyr Phe Tyr Val Ala Glu Ile Cys Pro His Leu 1145 1150 1155 tcc cca ctc agc tgc ttc cct ggt gac aac tac cgc acg ttc aag 3519 Ser Pro Leu Ser Cys Phe Pro Gly Asp Asn Tyr Arg Thr Phe Lys 1160 1165 1170 cac tac tac ctc gtc aag tat ggt ctg acc ata cag aat acc tcg 3564 His Tyr Tyr Leu Val Lys Tyr Gly Leu Thr Ile Gln Asn Thr Ser 1175 1180 1185 cag ccg cta ttg gac gtg gat cac acc agt gcg cgg tta aac ttc 3609 Gln Pro Leu Leu Asp Val Asp His Thr Ser Ala Arg Leu Asn Phe 1190 1195 1200 ctc acg cca cga tac gtt aat cgc aag ggc gtt gct ctg ccc act 3654 Leu Thr Pro Arg Tyr Val Asn Arg Lys Gly Val Ala Leu Pro Thr 1205 1210 1215 agt tcg gag gag aca aag cgg gca aag cgc gag aat ctc gaa cag 3699 Ser Ser Glu Glu Thr Lys Arg Ala Lys Arg Glu Asn Leu Glu Gln 1220 1225 1230 aag cag atc ctt gtg cca gag ctc tgc act gtg cat cca ttc ccc 3744 Lys Gln Ile Leu Val Pro Glu Leu Cys Thr Val His Pro Phe Pro 1235 1240 1245 gcc tcc ttg tgg cga act gcc gtg tgc ctg ccc tgc atc ctg tac 3789 Ala Ser Leu Trp Arg Thr Ala Val Cys Leu Pro Cys Ile Leu Tyr 1250 1255 1260 cgc ata aat ggt ctt cta ttg gcc gac gat att cgg aaa cag gtt 3834 Arg Ile Asn Gly Leu Leu Leu Ala Asp Asp Ile Arg Lys Gln Val 1265 1270 1275 tct gcg gat ctg ggg ctg gga agg caa cag atc gaa gat gag gat 3879 Ser Ala Asp Leu Gly Leu Gly Arg Gln Gln Ile Glu Asp Glu Asp 1280 1285 1290 ttc gag tgg ccc atg ctg gac ttt ggg tgg agt cta tcg gag gtg 3924 Phe Glu Trp Pro Met Leu Asp Phe Gly Trp Ser Leu Ser Glu Val 1295 1300 1305 ctc aag aaa tcg cgg gag tcc aaa caa aag gag tcc ctt aag gat 3969 Leu Lys Lys Ser Arg Glu Ser Lys Gln Lys Glu Ser Leu Lys Asp 1310 1315 1320 gat act att aat ggc aaa gac tta gct gat gtt gaa aag aaa ccg 4014 Asp Thr Ile Asn Gly Lys Asp Leu Ala Asp Val Glu Lys Lys Pro 1325 1330 1335 act agc gag gag acc caa cta gat aag gat tca aaa gac gat aag 4059 Thr Ser Glu Glu Thr Gln Leu Asp Lys Asp Ser Lys Asp Asp Lys 1340 1345 1350 gtt gag aaa agt gct att gaa cta atc att gag gga gag gag aag 4104 Val Glu Lys Ser Ala Ile Glu Leu Ile Ile Glu Gly Glu Glu Lys 1355 1360 1365 ctg caa gag gct gat gac ttc att gag ata ggc act tgg tca aac 4149 Leu Gln Glu Ala Asp Asp Phe Ile Glu Ile Gly Thr Trp Ser Asn 1370 1375 1380 gat atg gcc gac gat ata gct agt ttt aac caa gaa gac gac gac 4194 Asp Met Ala Asp Asp Ile Ala Ser Phe Asn Gln Glu Asp Asp Asp 1385 1390 1395 gag gat gac gcc ttc cat ctc cca gtt tta ccg gca aac gtt aag 4239 Glu Asp Asp Ala Phe His Leu Pro Val Leu Pro Ala Asn Val Lys 1400 1405 1410 ttc tgt gat cag caa acg cgc tac ggt tcg ccc aca ttt tgg gat 4284 Phe Cys Asp Gln Gln Thr Arg Tyr Gly Ser Pro Thr Phe Trp Asp 1415 1420 1425 gtg agc aat ggc gaa agc ggc ttc aag ggt cca aag agc agt cag 4329 Val Ser Asn Gly Glu Ser Gly Phe Lys Gly Pro Lys Ser Ser Gln 1430 1435 1440 aat aag cag ggt ggc aag ggc aaa gca aag ggt ccg gca aag ccc 4374 Asn Lys Gln Gly Gly Lys Gly Lys Ala Lys Gly Pro Ala Lys Pro 1445 1450 1455 aca ttt aac tat tat gac tcg gac aat tcg ctg ggt tcc agc tac 4419 Thr Phe Asn Tyr Tyr Asp Ser Asp Asn Ser Leu Gly Ser Ser Tyr 1460 1465 1470 gat gac gac gat aac gca ggt ccg ctc aat tac atg cat cac aac 4464 Asp Asp Asp Asp Asn Ala Gly Pro Leu Asn Tyr Met His His Asn 1475 1480 1485 tac agt tcg gat gac gac gat gtg gca gat gat atc gat gcg gga 4509 Tyr Ser Ser Asp Asp Asp Asp Val Ala Asp Asp Ile Asp Ala Gly 1490 1495 1500 cgc att gcg ttc acc tcc aag aat gaa gcg gag act att gaa acc 4554 Arg Ile Ala Phe Thr Ser Lys Asn Glu Ala Glu Thr Ile Glu Thr 1505 1510 1515 gca cag gaa gtg gaa aag cgc cag aag cag ctg tcc atc atc cag 4599 Ala Gln Glu Val Glu Lys Arg Gln Lys Gln Leu Ser Ile Ile Gln 1520 1525 1530 gcg acc aat gct aac gag cgg cag tat cag cag aca aag aac ctg 4644 Ala Thr Asn Ala Asn Glu Arg Gln Tyr Gln Gln Thr Lys Asn Leu 1535 1540 1545 ctc att gga ttc aat ttt aag cat gag gac cag aag gaa cct gcc 4689 Leu Ile Gly Phe Asn Phe Lys His Glu Asp Gln Lys Glu Pro Ala 1550 1555 1560 act ata aga tat gaa gaa tcc ata gct aag ctc aaa acg gaa ata 4734 Thr Ile Arg Tyr Glu Glu Ser Ile Ala Lys Leu Lys Thr Glu Ile 1565 1570 1575 gaa tcc ggc ggc atg ttg gtg ccg cac gac cag cag ttg gtt cta 4779 Glu Ser Gly Gly Met Leu Val Pro His Asp Gln Gln Leu Val Leu 1580 1585 1590 aaa aga agt gat gcc gct gag gct cag gtt gca aag gta tcg atg 4824 Lys Arg Ser Asp Ala Ala Glu Ala Gln Val Ala Lys Val Ser Met 1595 1600 1605 atg gag cta ttg aag cag ctg ctg ccg tat gta aat gaa gat gtg 4869 Met Glu Leu Leu Lys Gln Leu Leu Pro Tyr Val Asn Glu Asp Val 1610 1615 1620 ctg gcc aaa aag ctg ggt gat agg cgc gag ctt ctg ctg tcg gat 4914 Leu Ala Lys Lys Leu Gly Asp Arg Arg Glu Leu Leu Leu Ser Asp 1625 1630 1635 ttg gta gag cta aat gca gat tgg gta gcg cga cat gag cag gag 4959 Leu Val Glu Leu Asn Ala Asp Trp Val Ala Arg His Glu Gln Glu 1640 1645 1650 acc tac aat gta atg gga tgc gga gat agt ttt gac aac tat aac 5004 Thr Tyr Asn Val Met Gly Cys Gly Asp Ser Phe Asp Asn Tyr Asn 1655 1660 1665 gat cat cat cgg ctg aac ttg gat gaa aag caa ctg aaa ctg caa 5049 Asp His His Arg Leu Asn Leu Asp Glu Lys Gln Leu Lys Leu Gln 1670 1675 1680 tac gaa cga att gaa att gag cca cct act tcc acg aag gcc ata 5094 Tyr Glu Arg Ile Glu Ile Glu Pro Pro Thr Ser Thr Lys Ala Ile 1685 1690 1695 acc tca gcc ata tta cca gct ggc ttc agt ttc gat cga caa ccg 5139 Thr Ser Ala Ile Leu Pro Ala Gly Phe Ser Phe Asp Arg Gln Pro 1700 1705 1710 gat cta gtg ggc cat cca gga ccc agt ccc agc atc att ttg caa 5184 Asp Leu Val Gly His Pro Gly Pro Ser Pro Ser Ile Ile Leu Gln 1715 1720 1725 gcc ctc aca atg tcc aat gct aac gat ggc atc aat ctg gag cga 5229 Ala Leu Thr Met Ser Asn Ala Asn Asp Gly Ile Asn Leu Glu Arg 1730 1735 1740 ctg gag aca att gga gat tcc ttt cta aag tat gcc att acc acc 5274 Leu Glu Thr Ile Gly Asp Ser Phe Leu Lys Tyr Ala Ile Thr Thr 1745 1750 1755 tac ttg tac atc acc tac gag aat gtg cac gag gga aaa cta agt 5319 Tyr Leu Tyr Ile Thr Tyr Glu Asn Val His Glu Gly Lys Leu Ser 1760 1765 1770 cac ctg cgc tcc aag cag gtt gcc aat ctc aat ctc tat cgt ctg 5364 His Leu Arg Ser Lys Gln Val Ala Asn Leu Asn Leu Tyr Arg Leu 1775 1780 1785 ggc aga cgt aag aga ctg ggt gaa tat atg ata gcc act aaa ttc 5409 Gly Arg Arg Lys Arg Leu Gly Glu Tyr Met Ile Ala Thr Lys Phe 1790 1795 1800 gag ccg cac gac aat tgg ctg cca ccc tgc tac tac gtg cca aag 5454 Glu Pro His Asp Asn Trp Leu Pro Pro Cys Tyr Tyr Val Pro Lys 1805 1810 1815 gag cta gag aag gcg ctc atc gag gcg aag atc ccc act cac cat 5499 Glu Leu Glu Lys Ala Leu Ile Glu Ala Lys Ile Pro Thr His His 1820 1825 1830 tgg aag ctg gcc gat ctg cta gac att aag aac cta agc agt gtg 5544 Trp Lys Leu Ala Asp Leu Leu Asp Ile Lys Asn Leu Ser Ser Val 1835 1840 1845 caa atc tgc gag atg gtt cgc gaa aaa gcc gat gcc ctg ggc ttg 5589 Gln Ile Cys Glu Met Val Arg Glu Lys Ala Asp Ala Leu Gly Leu 1850 1855 1860 gag cag aat ggg ggt gcc caa aat gga caa ctt gac gac tcc aat 5634 Glu Gln Asn Gly Gly Ala Gln Asn Gly Gln Leu Asp Asp Ser Asn 1865 1870 1875 gat agc tgc aat gat ttt agc tgt ttt att ccc tac aac ctt gtt 5679 Asp Ser Cys Asn Asp Phe Ser Cys Phe Ile Pro Tyr Asn Leu Val 1880 1885 1890 tcg caa cac agc att ccg gat aag tct att gcc gat tgc gtc gaa 5724 Ser Gln His Ser Ile Pro Asp Lys Ser Ile Ala Asp Cys Val Glu 1895 1900 1905 gcc ctc att gga gcc tat ctc att gag tgc gga ccc cga ggg gct 5769 Ala Leu Ile Gly Ala Tyr Leu Ile Glu Cys Gly Pro Arg Gly Ala 1910 1915 1920 tta ctc ttt atg gcc tgg ctg ggc gtg aga gtg ctc cct atc aca 5814 Leu Leu Phe Met Ala Trp Leu Gly Val Arg Val Leu Pro Ile Thr 1925 1930 1935 agg cag ttg gac ggg ggt aac cag gag caa cga ata ccc ggt agc 5859 Arg Gln Leu Asp Gly Gly Asn Gln Glu Gln Arg Ile Pro Gly Ser 1940 1945 1950 aca aaa ccg aat gcc gaa aat gtg gtc acc gtt tac ggt gca tgg 5904 Thr Lys Pro Asn Ala Glu Asn Val Val Thr Val Tyr Gly Ala Trp 1955 1960 1965 ccc acg ccg cgt agt cca ctg ctg cac ttt gct cca aat gct acg 5949 Pro Thr Pro Arg Ser Pro Leu Leu His Phe Ala Pro Asn Ala Thr 1970 1975 1980 gag gag ctg gac cag tta cta agc ggc ttt gag gag ttt gag gag 5994 Glu Glu Leu Asp Gln Leu Leu Ser Gly Phe Glu Glu Phe Glu Glu 1985 1990 1995 agt ttg gga tac aag ttc cgg gat cgg tcg tac ctg ttg caa gcc 6039 Ser Leu Gly Tyr Lys Phe Arg Asp Arg Ser Tyr Leu Leu Gln Ala 2000 2005 2010 atg aca cat gcc agt tac acg ccc aat cga ttg acg gat tgc tat 6084 Met Thr His Ala Ser Tyr Thr Pro Asn Arg Leu Thr Asp Cys Tyr 2015 2020 2025 cag cgt ctg gag ttc ctg ggc gat gct gtt cta gat tac ctc att 6129 Gln Arg Leu Glu Phe Leu Gly Asp Ala Val Leu Asp Tyr Leu Ile 2030 2035 2040 acg cgg cat tta tac gaa gat ccc cgc cag cat tct cca ggc gca 6174 Thr Arg His Leu Tyr Glu Asp Pro Arg Gln His Ser Pro Gly Ala 2045 2050 2055 tta acg gat ttg cgg tca gca ctg gtg aat aat aca ata ttc gcc 6219 Leu Thr Asp Leu Arg Ser Ala Leu Val Asn Asn Thr Ile Phe Ala 2060 2065 2070 tcc ctg gct gtt cgc cat ggc ttc cac aag ttc ttc cgg cac ctc 6264 Ser Leu Ala Val Arg His Gly Phe His Lys Phe Phe Arg His Leu 2075 2080 2085 tcg ccg ggc ctt aac gat gtg att gac cgt ttt gtg cgg atc cag 6309 Ser Pro Gly Leu Asn Asp Val Ile Asp Arg Phe Val Arg Ile Gln 2090 2095 2100 cag gag aat gga cac tgc atc agt gag gag tac tac tta ttg tcc 6354 Gln Glu Asn Gly His Cys Ile Ser Glu Glu Tyr Tyr Leu Leu Ser 2105 2110 2115 gag gag gag tgc gat gac gcc gag gac gtt gag gtg ccc aag gca 6399 Glu Glu Glu Cys Asp Asp Ala Glu Asp Val Glu Val Pro Lys Ala 2120 2125 2130 ttg ggc gac gtt ttc gag tcg atc gca ggt gcc att ttt ctc gac 6444 Leu Gly Asp Val Phe Glu Ser Ile Ala Gly Ala Ile Phe Leu Asp 2135 2140 2145 tca aac atg tcg ctg gac gtg gtt tgg cac gta tat agc aac atg 6489 Ser Asn Met Ser Leu Asp Val Val Trp His Val Tyr Ser Asn Met 2150 2155 2160 atg agc ccg gag atc gag cag ttc agc aac tca gtg cca aaa tcg 6534 Met Ser Pro Glu Ile Glu Gln Phe Ser Asn Ser Val Pro Lys Ser 2165 2170 2175 ccc att cgg gag ctc ctc gag ctg gag ccg gaa acc gcc aag ttc 6579 Pro Ile Arg Glu Leu Leu Glu Leu Glu Pro Glu Thr Ala Lys Phe 2180 2185 2190 ggc aag ccc gag aag ctg gcg gat ggg cga cgg gtg cgc gtt acc 6624 Gly Lys Pro Glu Lys Leu Ala Asp Gly Arg Arg Val Arg Val Thr 2195 2200 2205 gtg gat gtc ttc tgc aaa gga acc ttc cgt ggc atc gga cgc aac 6669 Val Asp Val Phe Cys Lys Gly Thr Phe Arg Gly Ile Gly Arg Asn 2210 2215 2220 tat cgc att gcc aag tgc acg gcg gcc aaa tgc gca ttg cgc caa 6714 Tyr Arg Ile Ala Lys Cys Thr Ala Ala Lys Cys Ala Leu Arg Gln 2225 2230 2235 ctc aaa aag cag ggc ttg ata gcc aaa aaa gac taa 6750 Leu Lys Lys Gln Gly Leu Ile Ala Lys Lys Asp 2240 224542249PRTDrosophila melanogaster 4 Met Ala Phe His Trp Cys Asp Asn Asn Leu His Thr Thr Val Phe Thr 1 5 10 15 Pro Arg Asp Phe Gln Val Glu Leu Leu Ala Thr Ala Tyr Glu Arg Asn 20 25 30 Thr Ile Ile Cys Leu Gly His Arg Ser Ser Lys Glu Phe Ile Ala Leu 35 40 45 Lys Leu Leu Gln Glu Leu Ser Arg Arg Ala Arg Arg His Gly Arg Val 50 55 60 Ser Val Tyr Leu Ser Cys Glu Val Gly Thr Ser Thr Glu Pro Cys Ser 65 70 75 80 Ile Tyr Thr Met Leu Thr His Leu Thr Asp Leu Arg Val Trp Gln Glu 85 90 95 Gln Pro Asp Met Gln Ile Pro Phe Asp His Cys Trp Thr Asp Tyr His 100 105 110 Val Ser Ile Leu Arg Pro Glu Gly Phe Leu Tyr Leu Leu Glu Thr Arg 115 120 125 Glu Leu Leu Leu Ser Ser Val Glu Leu Ile Val Leu Glu Asp Cys His 130 135 140 Asp Ser Ala Val Tyr Gln Arg Ile Arg Pro Leu Phe Glu Asn His Ile 145 150 155 160 Met Pro Ala Pro Pro Ala Asp Arg Pro Arg Ile Leu Gly Leu Ala Gly 165 170 175 Pro Leu His Ser Ala Gly Cys Glu Leu Gln Gln Leu Ser Ala Met Leu 180 185 190 Ala Thr Leu Glu Gln Ser Val Leu Cys Gln Ile Glu Thr Ala Ser Asp 195 200 205 Ile Val Thr Val Leu Arg Tyr Cys Ser Arg Pro His Glu Tyr Ile Val 210 215 220 Gln Cys Ala Pro Phe Glu Met Asp Glu Leu Ser Leu Val Leu Ala Asp 225 230 235 240 Val Leu Asn Thr His Lys Ser Phe Leu Leu Asp His Arg Tyr Asp Pro 245 250 255 Tyr Glu Ile Tyr Gly Thr Asp Gln Phe Met Asp Glu Leu Lys Asp Ile 260 265 270 Pro Asp Pro Lys Val Asp Pro Leu Asn Val Ile Asn Ser Leu Leu Val 275 280 285 Val Leu His Glu Met Gly Pro Trp Cys Thr Gln Arg Ala Ala His His 290 295 300 Phe Tyr Gln Cys Asn Glu Lys Leu Lys Val Lys Thr Pro His Glu Arg 305 310 315 320 His Tyr Leu Leu Tyr Cys Leu Val Ser Thr Ala Leu Ile Gln Leu Tyr 325 330 335 Ser Leu Cys Glu His Ala Phe His Arg His Leu Gly Ser Gly Ser Asp 340 345 350 Ser Arg Gln Thr Ile Glu Arg Tyr Ser Ser Pro Lys Val Arg Arg Leu 355 360 365 Leu Gln Thr Leu Arg Cys Phe Lys Pro Glu Glu Val His Thr Gln Ala 370 375 380 Asp Gly Leu Arg Arg Met Arg His Gln Val Asp Gln Ala Asp Phe Asn 385 390 395 400 Arg Leu Ser His Thr Leu Glu Ser Lys Cys Arg Met Val Asp Gln Met 405 410 415 Asp Gln Pro Pro Thr Glu Thr Arg Ala Leu Val Ala Thr Leu Glu Gln 420 425 430 Ile Leu His Thr Thr Glu Asp Arg Gln Thr Asn Arg Ser Ala Ala Arg 435 440 445 Val Thr Pro Thr Pro Thr Pro Ala His Ala Lys Pro Lys Pro Ser Ser 450 455 460 Gly Ala Asn Thr Ala Gln Pro Arg Thr Arg Arg Arg Val Tyr Thr Arg 465 470 475 480 Arg His His Arg Asp His Asn Asp Gly Ser Asp Thr Leu Cys Ala Leu 485 490 495 Ile Tyr Cys Asn Gln Asn His Thr Ala Arg Val Leu Phe Glu Leu Leu 500 505 510 Ala Glu Ile Ser Arg Arg Asp Pro Asp Leu Lys Phe Leu Arg Cys Gln 515 520 525 Tyr Thr Thr Asp Arg Val Ala Asp Pro Thr Thr Glu Pro Lys Glu Ala 530 535 540 Glu Leu Glu His Arg Arg Gln Glu Glu Val Leu Lys Arg Phe Arg Met 545 550 555 560 His Asp Cys Asn Val Leu Ile Gly Thr Ser Val Leu Glu Glu Gly Ile 565 570 575 Asp Val Pro Lys Cys Asn Leu Val Val Arg Trp Asp Pro Pro Thr Thr 580 585 590 Tyr Arg Ser Tyr Val Gln Cys Lys Gly Arg Ala Arg Ala Ala Pro Ala 595 600 605 Tyr His Val Ile Leu Val Ala Pro Ser Tyr Lys Ser Pro Thr Val Gly 610 615 620 Ser Val Gln Leu Thr Asp Arg Ser His Arg Tyr Ile Cys Ala Thr Gly 625 630 635 640 Asp Thr Thr Glu Ala Asp Ser Asp Ser Asp Asp Ser Ala Met Pro Asn 645 650 655 Ser Ser Gly Ser Asp Pro Tyr Thr Phe Gly Thr Ala Arg Gly Thr Val 660 665 670 Lys Ile Leu Asn Pro Glu Val Phe Ser Lys Gln Pro Pro Thr Ala Cys 675 680 685 Asp Ile Lys Leu Gln Glu Ile Gln Asp Glu Leu Pro Ala Ala Ala Gln 690 695 700 Leu Asp Thr Ser Asn Ser Ser Asp Glu Ala Val Ser Met Ser Asn Thr 705 710 715 720 Ser Pro Ser Glu Ser Ser Thr Glu Gln Lys Ser Arg Arg Phe Gln Cys 725 730 735 Glu Leu Ser Ser Leu Thr Glu Pro Glu Asp Thr Ser Asp Thr Thr Ala 740 745 750 Glu Ile Asp Thr Ala His Ser Leu Ala Ser Thr Thr Lys Asp Leu Val 755 760 765 His Gln Met Ala Gln Tyr Arg Glu Ile Glu Gln Met Leu Leu Ser Lys 770 775 780 Cys Ala Asn Thr Glu Pro Pro Glu Gln Glu Gln Ser Glu Ala Glu Arg 785 790 795 800 Phe Ser Ala Cys Leu Ala Ala Tyr Arg Pro Lys Pro His Leu Leu Thr 805 810 815 Gly Ala Ser Val Asp Leu Gly Ser Ala Ile Ala Leu Val Asn Lys Tyr 820 825 830 Cys Ala Arg Leu Pro Ser Asp Thr Phe Thr Lys Leu Thr Ala Leu Trp 835 840 845 Arg Cys Thr Arg Asn Glu Arg Ala Gly Val Thr Leu Phe Gln Tyr Thr 850 855 860 Leu Arg Leu Pro Ile Asn Ser Pro Leu Lys His Asp Ile Val Gly Leu 865 870 875 880 Pro Met Pro Thr Gln Thr Leu Ala Arg Arg Leu Ala Ala Leu Gln Ala 885 890 895 Cys Val Glu Leu His Arg Ile Gly Glu Leu Asp Asp Gln Leu Gln Pro 900 905 910 Ile Gly Lys Glu Gly Phe Arg Ala Leu Glu Pro Asp Trp Glu Cys Phe 915 920 925 Glu Leu Glu Pro Glu Asp Glu Gln Ile Val Gln Leu Ser Asp Glu Pro 930 935 940 Arg Pro Gly Thr Thr Lys Arg Arg Gln Tyr Tyr Tyr Lys Arg Ile Ala 945 950 955 960 Ser Glu Phe Cys Asp Cys Arg Pro Val Ala Gly Ala Pro Cys Tyr Leu 965 970 975 Tyr Phe Ile Gln Leu Thr Leu Gln Cys Pro Ile Pro Glu Glu Gln Asn 980 985 990 Thr Arg Gly Arg Lys Ile Tyr Pro Pro Glu Asp Ala Gln Gln Gly Phe 995 1000 1005 Gly Ile Leu Thr Thr Lys Arg Ile Pro Lys Leu Ser Ala Phe Ser 1010 1015 1020 Ile Phe Thr Arg Ser Gly Glu Val Lys Val Ser Leu Glu Leu Ala 1025 1030 1035 Lys Glu Arg Val Ile Leu Thr Ser Glu Gln Ile Val Cys Ile Asn 1040 1045 1050 Gly Phe Leu Asn Tyr Thr Phe Thr Asn Val Leu Arg Leu Gln Lys 1055 1060 1065 Phe Leu Met Leu Phe Asp Pro Asp Ser Thr Glu Asn Cys Val Phe 1070 1075 1080 Ile Val Pro Thr Val Lys Ala Pro Ala Gly Gly Lys His Ile Asp 1085 1090 1095 Trp Gln Phe Leu Glu Leu Ile Gln Ala Asn Gly Asn Thr Met Pro 1100 1105 1110 Arg Ala Val Pro Asp Glu Glu Arg Gln Ala Gln Pro Phe Asp Pro 1115 1120 1125 Gln Arg Phe Gln Asp Ala Val Val Met Pro Trp Tyr Arg Asn Gln 1130 1135 1140 Asp Gln Pro Gln Tyr Phe Tyr Val Ala Glu Ile Cys Pro His Leu 1145 1150 1155 Ser Pro Leu Ser Cys Phe Pro Gly Asp Asn Tyr Arg Thr Phe Lys 1160 1165 1170 His Tyr Tyr Leu Val Lys Tyr Gly Leu Thr Ile Gln Asn Thr Ser 1175 1180 1185 Gln Pro Leu Leu Asp Val Asp His Thr Ser Ala Arg Leu Asn Phe 1190 1195 1200 Leu Thr Pro Arg Tyr Val Asn Arg Lys Gly Val Ala Leu Pro Thr 1205 1210 1215 Ser Ser Glu Glu Thr Lys Arg Ala Lys Arg Glu Asn Leu Glu Gln 1220 1225 1230 Lys Gln Ile Leu Val Pro Glu Leu Cys Thr Val His Pro Phe Pro 1235 1240 1245 Ala Ser Leu Trp Arg Thr Ala Val Cys Leu Pro Cys Ile Leu Tyr 1250 1255 1260 Arg Ile Asn Gly Leu Leu Leu Ala Asp Asp Ile Arg Lys Gln Val 1265 1270 1275 Ser Ala Asp Leu Gly Leu Gly Arg Gln Gln Ile Glu Asp Glu Asp 1280 1285 1290 Phe Glu Trp Pro Met Leu Asp Phe Gly Trp Ser Leu Ser Glu Val 1295 1300 1305 Leu Lys Lys Ser Arg Glu Ser Lys Gln Lys Glu Ser Leu Lys Asp 1310 1315 1320 Asp Thr Ile Asn Gly Lys Asp Leu Ala Asp Val Glu Lys Lys Pro 1325 1330 1335 Thr Ser Glu Glu Thr Gln Leu Asp Lys Asp Ser Lys Asp Asp Lys 1340 1345 1350 Val Glu Lys Ser Ala Ile Glu Leu Ile Ile Glu Gly Glu Glu Lys 1355 1360 1365 Leu Gln Glu Ala Asp Asp Phe Ile Glu Ile Gly Thr Trp Ser Asn 1370 1375 1380 Asp Met Ala Asp Asp Ile Ala Ser Phe Asn Gln Glu Asp Asp Asp 1385 1390 1395 Glu Asp Asp Ala Phe His Leu Pro Val Leu Pro Ala Asn Val Lys 1400 1405 1410 Phe Cys Asp Gln Gln Thr Arg Tyr Gly Ser Pro Thr Phe Trp Asp 1415 1420 1425 Val Ser Asn Gly Glu Ser Gly Phe Lys Gly Pro Lys Ser Ser Gln 1430 1435 1440 Asn Lys Gln Gly Gly Lys Gly Lys Ala Lys Gly Pro Ala Lys Pro 1445 1450 1455 Thr Phe Asn Tyr Tyr Asp Ser Asp Asn Ser Leu Gly Ser Ser Tyr 1460 1465 1470 Asp Asp Asp Asp Asn Ala Gly Pro Leu Asn Tyr Met His His Asn 1475 1480 1485 Tyr Ser Ser Asp Asp Asp Asp Val Ala Asp Asp Ile Asp Ala Gly 1490 1495 1500 Arg Ile Ala Phe Thr Ser Lys Asn Glu Ala Glu Thr Ile Glu Thr 1505 1510 1515 Ala Gln Glu Val Glu Lys Arg Gln Lys Gln Leu Ser Ile Ile Gln 1520 1525 1530 Ala Thr Asn Ala Asn Glu Arg Gln Tyr Gln Gln Thr Lys Asn Leu 1535 1540 1545 Leu Ile Gly Phe Asn Phe Lys His Glu Asp Gln Lys Glu Pro Ala 1550 1555 1560 Thr Ile Arg Tyr Glu Glu Ser Ile Ala Lys Leu Lys Thr Glu Ile 1565 1570 1575 Glu Ser Gly Gly Met Leu Val Pro His Asp Gln Gln Leu Val Leu 1580 1585 1590 Lys Arg Ser Asp Ala Ala Glu Ala Gln Val Ala Lys Val Ser Met 1595 1600 1605 Met Glu Leu Leu Lys Gln Leu Leu Pro Tyr Val Asn Glu Asp Val 1610 1615 1620 Leu Ala Lys Lys Leu Gly Asp Arg Arg Glu Leu Leu Leu Ser Asp 1625 1630 1635 Leu Val Glu Leu Asn Ala Asp Trp Val Ala Arg His Glu Gln Glu 1640 1645 1650 Thr Tyr Asn Val Met Gly Cys Gly Asp Ser Phe Asp Asn Tyr Asn 1655 1660 1665 Asp His His Arg Leu Asn Leu Asp Glu Lys Gln Leu Lys Leu Gln 1670 1675 1680 Tyr Glu Arg Ile Glu Ile Glu Pro Pro Thr Ser Thr Lys Ala Ile 1685 1690 1695 Thr Ser Ala Ile Leu Pro Ala Gly Phe Ser Phe Asp Arg Gln Pro 1700 1705 1710 Asp Leu Val Gly His Pro Gly Pro Ser Pro Ser Ile Ile Leu Gln 1715 1720 1725 Ala Leu Thr Met Ser Asn Ala Asn Asp Gly Ile Asn Leu Glu Arg 1730 1735 1740 Leu Glu Thr Ile Gly Asp Ser Phe Leu Lys Tyr Ala Ile Thr Thr 1745 1750 1755 Tyr Leu Tyr Ile Thr Tyr Glu Asn Val His Glu Gly Lys Leu Ser 1760 1765 1770 His Leu Arg Ser Lys Gln Val Ala Asn Leu Asn Leu Tyr Arg Leu 1775 1780 1785 Gly Arg Arg Lys Arg Leu Gly Glu Tyr Met Ile Ala Thr Lys Phe 1790 1795 1800 Glu Pro His Asp Asn Trp Leu Pro Pro Cys Tyr Tyr Val Pro Lys 1805 1810 1815 Glu Leu Glu Lys Ala Leu Ile Glu Ala Lys Ile Pro Thr His His 1820 1825 1830 Trp Lys Leu Ala Asp Leu Leu Asp Ile Lys Asn Leu Ser Ser Val 1835 1840 1845 Gln Ile Cys Glu Met Val Arg Glu Lys Ala Asp Ala Leu Gly Leu 1850 1855 1860 Glu Gln Asn Gly Gly Ala Gln Asn Gly Gln Leu Asp Asp Ser Asn 1865 1870 1875 Asp Ser Cys Asn Asp Phe Ser Cys Phe Ile Pro Tyr Asn Leu Val 1880 1885 1890 Ser Gln His Ser Ile Pro Asp Lys Ser Ile Ala Asp Cys Val Glu 1895 1900 1905 Ala Leu Ile Gly Ala Tyr Leu Ile Glu Cys Gly Pro Arg Gly Ala 1910 1915 1920 Leu Leu Phe Met Ala Trp Leu Gly Val Arg Val Leu Pro Ile Thr 1925 1930 1935 Arg Gln Leu Asp Gly Gly Asn Gln Glu Gln Arg Ile Pro Gly Ser 1940 1945 1950 Thr Lys Pro Asn Ala Glu Asn Val Val Thr Val Tyr Gly Ala Trp 1955 1960 1965 Pro Thr Pro Arg Ser Pro Leu Leu His Phe Ala Pro Asn Ala Thr 1970 1975 1980 Glu Glu Leu Asp Gln Leu Leu Ser Gly Phe Glu Glu Phe Glu Glu 1985 1990 1995 Ser Leu Gly Tyr Lys Phe Arg Asp Arg Ser Tyr Leu Leu Gln Ala 2000 2005 2010 Met Thr His Ala Ser Tyr Thr Pro Asn Arg Leu Thr Asp Cys Tyr 2015 2020 2025 Gln Arg Leu Glu Phe Leu Gly Asp Ala Val Leu Asp Tyr Leu Ile 2030 2035 2040 Thr Arg His Leu Tyr Glu Asp Pro Arg Gln His Ser Pro Gly Ala 2045 2050 2055 Leu Thr Asp Leu Arg Ser Ala Leu Val Asn Asn Thr Ile Phe Ala 2060 2065 2070 Ser Leu Ala Val Arg His Gly Phe His Lys Phe Phe Arg His Leu 2075 2080 2085 Ser Pro Gly Leu Asn Asp Val Ile Asp Arg Phe Val Arg Ile Gln 2090 2095 2100 Gln Glu Asn Gly His Cys Ile Ser Glu Glu Tyr Tyr Leu Leu Ser 2105 2110 2115 Glu Glu Glu Cys Asp Asp Ala Glu Asp Val Glu Val Pro Lys Ala 2120 2125 2130 Leu Gly Asp Val Phe Glu Ser Ile Ala Gly Ala Ile Phe Leu Asp 2135 2140 2145 Ser Asn Met Ser Leu Asp Val Val Trp His Val Tyr Ser Asn Met 2150 2155 2160 Met Ser Pro Glu Ile Glu Gln Phe Ser Asn Ser Val Pro Lys Ser 2165 2170 2175 Pro Ile Arg Glu Leu Leu Glu Leu Glu Pro Glu Thr Ala Lys Phe 2180 2185 2190 Gly Lys Pro Glu Lys Leu Ala Asp Gly Arg Arg Val Arg Val Thr 2195 2200 2205 Val Asp Val Phe Cys Lys Gly Thr Phe Arg Gly Ile Gly Arg Asn 2210 2215 2220 Tyr Arg Ile Ala Lys Cys Thr Ala Ala Lys Cys Ala Leu Arg Gln 2225 2230 2235 Leu Lys Lys Gln Gly Leu Ile Ala Lys Lys Asp 2240 224551145PRTDrosophila melanogaster 5 Met Gly Lys Lys Asp Lys Asn Lys Lys Gly Gly Gln Asp Ser Ala Ala 1 5 10 15 Ala Pro Gln Pro Gln Gln Gln Gln Lys Gln Gln Gln Gln Arg Gln Gln 20 25 30 Gln Pro Gln Gln Leu Gln Gln Pro Gln Gln Leu Gln Gln Pro Gln Gln 35 40 45 Leu Gln Gln Pro Gln Gln Gln Gln Gln Gln Gln Pro His Gln Gln Gln 50 55 60 Gln Gln Ser Ser Arg Gln Gln Pro Ser Thr Ser Ser Gly Gly Ser Arg 65 70 75 80 Ala Ser Gly Phe Gln Gln Gly Gly Gln Gln Gln Lys Ser Gln Asp Ala 85 90 95 Glu Gly Trp Thr Ala Gln Lys Lys Gln Gly Lys Gln Gln Val Gln Gly 100 105 110 Trp Thr Lys Gln Gly Gln Gln Gly Gly His Gln Gln Gly Arg Gln Gly 115 120 125 Gln Asp Gly Gly Tyr Gln Gln Arg Pro Pro Gly Gln Gln Gln Gly Gly 130 135 140 His Gln Gln Gly Arg Gln Gly Gln Glu Gly Gly Tyr Gln Gln Arg Pro 145 150 155 160 Pro Gly Gln Gln Gln Gly Gly His Gln Gln Gly Arg Gln Gly Gln Glu 165 170 175 Gly Gly Tyr Gln Gln Arg Pro Ser Gly Gln Gln Gln Gly Gly His Gln 180 185 190 Gln Gly Arg Gln Gly Gln Glu Gly Gly Tyr Gln Gln Arg Pro Pro Gly 195 200 205 Gln Gln Gln Gly Gly His Gln Gln Gly Arg Gln Gly Gln Glu Gly Gly 210 215 220 Tyr Gln Gln Arg Pro Ser Gly Gln Gln Gln Gly Gly His Gln Gln Gly 225 230 235 240 Arg Gln Gly Gln Glu Gly Gly Tyr Gln Gln Arg Pro Ser Gly Gln Gln 245 250 255 Gln Gly Gly His Gln Gln Gly Arg Gln Gly Gln Glu Gly Gly Tyr Gln 260 265 270 Gln Arg Pro Ser Gly Gln Gln Gln Gly Gly His Gln Gln Gly Arg Gln 275 280 285 Gly Gln Glu Gly Gly Tyr Gln Gln Arg Pro Pro Gly Gln Gln Pro Asn 290 295 300 Gln Thr Gln Ser Gln Gly Gln Tyr Gln Ser Arg Gly Pro Pro Gln Gln 305 310 315 320 Gln Gln Ala Ala Pro Leu Pro Leu Pro Pro Gln Pro Ala Gly Ser Ile 325 330 335 Lys Arg Gly Thr Ile Gly Lys Pro Gly Gln Val Gly Ile Asn Tyr Leu 340 345 350 Asp Leu Asp Leu Ser Lys Met Pro Ser Val Ala Tyr His Tyr Asp Val 355 360 365 Lys Ile Met Pro Glu Arg Pro Lys Lys Phe Tyr Arg Gln Ala Phe Glu 370 375 380 Gln Phe Arg Val Asp Gln Leu Gly Gly Ala Val Leu Ala Tyr Asp Gly 385 390 395 400 Lys Ala Ser Cys Tyr Ser Val Asp Lys Leu Pro Leu Asn Ser Gln Asn 405 410 415 Pro Glu Val Thr Val Thr Asp Arg Asn Gly Arg Thr Leu Arg Tyr Thr 420 425 430 Ile Glu Ile Lys Glu Thr Gly Asp Ser Thr Ile Asp Leu Lys Ser Leu 435 440 445 Thr Thr Tyr Met Asn Asp Arg Ile Phe Asp Lys Pro Met Arg Ala Met 450 455 460 Gln Cys Val Glu Val Val Leu Ala Ser Pro Cys His Asn Lys Ala Ile 465 470 475 480 Arg Val Gly Arg Ser Phe Phe Lys Met Ser Asp Pro Asn Asn Arg His 485 490 495 Glu Leu Asp Asp Gly Tyr Glu Ala Leu Val Gly Leu Tyr Gln Ala Phe 500 505 510 Met Leu Gly Asp Arg Pro Phe Leu Asn Val Asp Ile Ser His Lys Ser 515 520 525 Phe Pro Ile Ser Met Pro Met Ile Glu Tyr Leu Glu Arg Phe Ser Leu 530 535 540 Lys Ala Lys Ile Asn Asn Thr Thr Asn Leu Asp Tyr Ser Arg Arg Phe 545 550 555 560 Leu Glu Pro Phe Leu Arg Gly Ile Asn Val Val Tyr Thr Pro Pro Gln 565 570 575 Ser Phe Gln Ser Ala Pro Arg Val Tyr Arg Val Asn Gly Leu Ser Arg 580 585 590 Ala Pro Ala Ser Ser Glu Thr Phe Glu His Asp Gly Lys Lys Val Thr 595 600 605 Ile Ala Ser Tyr Phe His Ser Arg Asn Tyr Pro Leu Lys Phe Pro Gln 610 615 620 Leu His Cys Leu Asn Val Gly Ser Ser Ile Lys Ser Ile Leu Leu Pro 625 630 635 640 Ile Glu Leu Cys Ser Ile Glu Glu Gly Gln Ala Leu Asn Arg Lys Asp 645 650 655 Gly Ala Thr Gln Val Ala Asn Met Ile Lys Tyr Ala Ala Thr Ser Thr 660 665 670 Asn Val Arg Lys Arg Lys Ile Met Asn Leu Leu Gln Tyr Phe Gln His 675 680 685 Asn Leu Asp Pro Thr Ile Ser Arg Phe Gly Ile Arg Ile Ala Asn Asp 690 695 700 Phe Ile Val Val Ser Thr Arg Val Leu Ser Pro Pro Gln Val Glu Tyr 705 710 715 720 His Ser Lys Arg Phe Thr Met Val Lys Asn Gly Ser Trp Arg Met Asp 725 730 735 Gly Met Lys Phe Leu Glu Pro Lys Pro Lys Ala His Lys Cys Ala Val 740 745 750 Leu Tyr Cys Asp Pro Arg Ser Gly Arg Lys Met Asn Tyr Thr Gln Leu 755 760 765 Asn Asp Phe Gly Asn Leu Ile Ile Ser Gln Gly Lys Ala Val Asn Ile 770 775 780 Ser Leu Asp Ser Asp Val Thr Tyr Arg Pro Phe Thr Asp Asp Glu Arg 785 790 795 800 Ser Leu Asp Thr Ile Phe Ala Asp Leu Lys Arg Ser Gln His Asp Leu 805 810 815 Ala Ile Val Ile Ile Pro Gln Phe Arg Ile Ser Tyr Asp Thr Ile Lys 820 825 830 Gln Lys Ala Glu Leu Gln His Gly Ile Leu Thr Gln Cys Ile Lys Gln 835 840 845 Phe Thr Val Glu Arg Lys Cys Asn Asn Gln Thr Ile Gly Asn Ile Leu 850 855 860 Leu Lys Ile Asn Ser Lys Leu Asn Gly Ile Asn His Lys Ile Lys Asp 865 870 875 880 Asp Pro Arg Leu Pro Met Met Lys Asn Thr Met Tyr Ile Gly Ala Asp 885 890 895 Val Thr His Pro Ser Pro Asp Gln Arg Glu Ile Pro Ser Val Val Gly 900 905 910 Val Ala Ala Ser His Asp Pro Tyr Gly Ala Ser Tyr Asn Met Gln Tyr 915 920 925 Arg Leu Gln Arg Gly Ala Leu Glu Glu Ile Glu Asp Met Phe Ser Ile 930 935 940 Thr Leu Glu His Leu Arg Val Tyr Lys Glu Tyr Arg Asn Ala Tyr Pro 945 950 955 960 Asp His Ile Ile Tyr Tyr Arg Asp Gly Val Ser Asp Gly Gln Phe Pro 965 970 975 Lys Ile Lys Asn Glu Glu Leu Arg Cys Ile Lys Gln Ala Cys Asp Lys 980 985 990 Val Gly Cys Lys Pro Lys Ile Cys Cys Val Ile Val Val Lys Arg His 995 1000 1005 His Thr Arg Phe Phe Pro Ser Gly Asp Val Thr Thr Ser Asn Lys 1010 1015 1020 Phe Asn Asn Val Asp Pro Gly Thr Val Val Asp Arg Thr Ile Val 1025 1030 1035 His Pro Asn Glu Met Gln Phe Phe Met Val Ser Gly Gln Ala Ile 1040 1045 1050 Gln Gly Thr Ala Lys Pro Thr Arg Tyr Asn Val Ile Glu Asn Thr 1055 1060 1065 Gly Asn Leu Asp Ile Asp Leu Leu Gln Gln Leu Thr Tyr Asn Leu 1070 1075 1080 Cys His Met Phe Pro Arg Cys Asn Arg Ser Val Ser Tyr Pro Ala 1085 1090 1095 Pro Ala Tyr Leu Ala His Leu Val Ala Ala Arg Gly Arg Val Tyr 1100 1105 1110 Leu Thr Gly Thr Asn Arg Phe Leu Asp Leu Lys Lys Glu Tyr Ala 1115 1120 1125 Lys Arg Thr Ile Val Pro Glu Phe Met Lys Lys Asn Pro Met Tyr 1130 1135 1140 Phe Val 1145622RNAphotinus pyralis 6 ucgaaguacu cagcguaagu ga 22722RNAphotinus pyralis 7 uaaagcuuca ugagucgcau uc 22883RNAphotinus pyralis 8 caucgacuga aaucccuccc ugguaauccg uuugggcucu gcccugcuau gggauaaaug 60 guuaucaggg auuuuagucg auc 83962RNAphotinus pyralis 9 caucgacuga aaucccuggu aauccguugu uaacaacgga uuaccaggga uuucagucga 60 ug 621044DNAArtificial Sequenceprimer 10 taatacgact cactataggg caaggtcata gttcctgcca gctg 441144DNAArtificial Sequenceprimer 11 taatacgact cactataggg cagatatttt cttaccaccc accc 441244DNAArtificial Sequenceprimer 12 taatacgact cactataggg ttaagtttaa caggagaagc tgga 441344DNAArtificial Sequenceprimer 13 taatacgact cactataggg aaatcattgc tttcctgata atgc 441444DNAArtificial Sequenceprimer 14 taatacgact cactataggg tagatttccg cagccccagt gttc 441544DNAArtificial Sequenceprimer 15 taatacgact cactataggg gttgcctctc atttttcctt gatt 441645DNAArtificial Sequenceprimer 16 taatacgact cactataggg tattttagac tgattacttt tataa 451744DNAArtificial Sequenceprimer 17 taatacgact cactataggg tcacatgttt tggctaagac ctat 441819DNADicer siRNA 18 tcaaccagcc actgctgga 191971DNAArtificial SequenceOligonucleotide Primer 19 tccaattcag cgggagccac ctgatgaagc ttgatcgggt ggctctcgct gagttggaat 60 ccattttttt t 712021RNAphotinus pyralis 20 ucgaaguacu cagcguaagu g 212121RNAPhotinus Pyralis 21 aaagcuucau gagucgcauu c 212281RNAPhotinus Pyralis 22 caucgacuga aaucccuggu aauccguuug gggcucugcc cugcuauggg auaaauggau 60 uaucagggau uuuagucgau g 812382RNAPhotinus Pyralis 23 caucgacuga aaucccgccg uaauccguuu ggggcucugc ccugcuaugg gauaaaugga 60 uuaucaggga uuuuagucga ug 822423RNAPhotinus Pyralis 24 ggucgaagua cucagcguaa gaa 232523DNAPhotinus Pyralis 25 aaagcuucat gagucgcauu cgg 232621RNAPhotinus Pyralis 26 gguuguggau cuggauaccg g 212721RNAPhotinus Pyralis 27 uuccaacacc uagaccuaug g 212821RNAPhotinus Pyralis 28 ggugccaacc cuauucuccu u 212921RNAPhotinus Pyralis 29 gaccacgguu gggauaagag g 213022RNAPhotinus Pyralis 30 ggcuaugaag agaguacgcc cu 223122RNAPhotinus Pyralis 31 uuccgauacu ucucucaugc gg 223264RNAPhotinus Pyralis 32 ggucgaagua cucagcguaa gugaugucca cuuaaguggg uguuguuugu guuggguguu 60 uugg 643360RNAPhotinus Pyralis 33 ggucgaagua cucagcguaa gugauguccu uaaggguguu guuuguguug gguguuuugg 603456RNAPhotinus Pyralis 34 gggcgaagua cucagcguaa gugauguuua aguguuguuu guguugggug uuuugg 563550RNAPhotinus Pyralis 35 ggucgaagua cucagcguaa gugauuaauu guuuguguug gguguuuugg 503669RNAPhotinus Pyralis 36 ggcucgaguc gaaguacuca gcguaaguga uguccauuaa guggguguug uuuguguugg 60 guguuuugg 693770RNAPhotinus Pyralis 37 ggucgaagua cucagcguaa gugaugucca cuuaaguggg uguuguuugu guuggguguu 60 uuggcucgag 703869RNAPhotinus Pyralis 38 ggauuccaau ucagcgggag ccaccugaug aagcuugauc ggguggcucu cgcugaguug 60 gaauccauu 693964RNAPhotinus Pyralis 39 ggucuaagug gagcccuucg aguguuagaa gcuugugaca cucggagggc uucacuuggg 60 ccuu 644021DNAPhotinus Pyralis 40 cuuacgcuga guacuucgat t 214121DNAPhotinus Pyralis 41 ucgaaguacu cagcguaagt t 214221DNAPhotinus Pyralis 42 agcuucauaa ggcgcaugct t 214321DNAPhotinus Pyralis 43 gcaugcgccu uaugaagcut t 214423DNAPhotinus Pyralis 44 cugugagauc uacggagccu gtt 234523DNAPhotinus Pyralis 45 caggcuccgu agaucucaca gtt 23

Claims (53)

We claim:

1. A method for attenuating expression of a target gene in host cells, comprising introducing double stranded RNA (dsRNA) into the host cells in an amount sufficient to attenuate expression of the target gene, wherein the dsRNA comprises a nucleotide sequence that hybridizes under stringent conditions to an untranslated sequence of the target gene.

2. A method for attenuating expression of a target gene in host cells, comprising introducing double stranded RNA (dsRNA) into the host cells in an amount sufficient to attenuate expression of the target gene, wherein the dsRNA comprises a nucleotide sequence that hybridizes under stringent conditions to an intronic sequence of the target gene.

3. A composition for attenuating expression of a target gene, comprising a double stranded RNA (dsRNA) having a nucleotide sequence that hybridizes under stringent conditions to an untranslated sequence of the target gene.

4. A composition for attenuating expression of a target gene, comprising an expression vector which, when expressed, produces a double stranded RNA (dsRNA) having a nucleotide sequence that hybridizes under stringent conditions to an untranslated sequence of the target gene.

5. A composition for attenuating expression of a target gene, comprising a double stranded RNA (dsRNA) having a nucleotide sequence that hybridizes under stringent conditions to an intronic sequence of the target gene.

6. A composition for attenuating expression of a target gene, comprising an expression vector which, when expressed, produces a double stranded RNA (dsRNA) having a nucleotide sequence that hybridizes under stringent conditions to an intronic sequence of the target gene.

7. The method ofclaim 1 or the composition ofclaim 3 or4, wherein the untranslated sequence of the target gene to which the dsRNA hybridizes is selected from the group consisting of a promoter sequence and an enhancer sequence.

8. The method of any of claims1 and2, wherein the host cells are suspended in culture.

9. The method of any of claims1 and2, wherein the host cells are in a whole animal.

10. The method of any of claims1 and2, wherein the target gene is a genomically integrated gene of the host cells.

11. The method of any of claims1 and2, wherein the target gene is a heterologous gene

12. The method ofclaim 11, wherein the target gene is a viral gene.

13. The method of any of claims1 and2, wherein the host cells is a primate cells.

14. The method ofclaim 13, wherein the host cells are human cells.

15. The method of any of claims1 and2, or the composition ofclaim 3 or5, wherein the dsRNA is short interfering double stranded RNA which does not produce a significant PKR-dependent response in the host cells at concentrations effective for attenuating expression of the target gene.

16. The method or the composition ofclaim 15, wherein the dsRNA is 15-45 basepairs in length.

17. The method or the composition ofclaim 15, wherein the dsRNA is 19-30 basepairs in length.

18. The method of any of claims1 and2, wherein the dsRNA is produced in the cell by an expression vector having a coding sequence that is transcribed to produce one or more transcriptional products that are processed to an siRNA species by said host cells.

19. The method of any of claims1 and2, or the composition ofclaim 3 or5, wherein the dsRNA is a hairpin RNA that is processed to an siRNA species by said host cells.

20. The method of any of claims1 and2, wherein expression of the target gene is attenuated by at least 10 fold.

21. A pharmaceutical package comprising:

a pharmaceutically preparation of a double stranded RNA (DSRNA) that is, or gives rise to, a short interfering double stranded RNA (siRNA) in a mammalian cell and attenuates expression of a target gene, which dsRNA does not produce a significant PKR-dependent response in the mammalian cell at concentrations effective for attenuating expression of the target gene; and

label or instructions (written and/or pictorial) for administering the preparation to a patient.

22. The pharmaceutical package ofclaim 21, wherein the siRNA hybridizes to an untranscribed sequence or an non-coding sequence of the target gene.

23. A method of attenuating expression of a target gene in the cells of a mammal, comprising administering the mammal a composition of any of claims3-6.

24. The method ofclaim 23, wherein attenuating expression of the target gene reduces unwanted growth or differentiation of the cells.

25. A method for generating short interfering double-stranded RNA (siRNA), comprising:

(i) providing an in vitro transcription system including:

a double-stranded nucleic acid having complementary sense and antisense target sequences, which target sequence is flanked by promoters for an RNA polymerase,

the RNA polymerase,

 wherein the sense and antisense target sequences are transcribed and can anneal to form an siRNA; and

(ii) isolating said siRNA from said in vitro transcription system.

26. The method ofclaim 25, wherein the RNA polymerase is a bacteriophage RNA polymerase.

27. The method ofclaim 26, wherein the RNA polymerase is selected from the group consisting of T3 polymerase, T7 polymerase and SP6 polymerase.

28. The method ofclaim 25, wherein the in vitro transcription system includes a variegated library of target sequences to produce a variegated library of siRNA species.

29. A method for performing a business of distributing short interfering double-stranded RNA (siRNA), comprising:

(i) accepting orders for siRNA species having a sequence designated by user;

(ii) providing an in vitro transcription system including:

a double-stranded nucleic acid having a target sequence of complementary sense and antisense sequences for said user designated siRNA species, which target sequence is flanked by promoters for an RNA polymerase, and

the RNA polymerase,

 wherein the sense and antisense target sequences are transcribed and can anneal to form an siRNA;

(iii) isolating said siRNA from said in vitro transcription system; and

(iv) packaging and shipping said siRNA to said user.

30. A method for altering the MHC phenotype of a donor stem cell or the progeny thereof, comprising introducing a double stranded RNA (dsRNA) into a stem cell in an amount sufficient to attenuate expression of an MHC gene otherwise expressed by said stem cell or the progeny thereof.

31. The method ofclaim 30, wherein the dsRNA reduces expression of one or more human leukocyte antigens (HLA) otherwise expressed by said stem cell or the progeny thereof.

32. A culture of donor stem cells or the progeny thereof, having an altered MHC phenotype resulting from stable attenuation of expression of one or more MHC genes by introduction of double stranded RNA (dsRNA) into the donor stem cells.

33. A method of transplanting a patient, comprising:

(i) generating an ex vivo cell or tissue culture of donor stem cells, or the progeny thereof, having an altered MHC phenotype resulting from stable attenuation of expression of one or more MHC genes by introduction of double stranded RNA (dsRNA) into the donor stem cells; and

(ii) transplanting said patient with said cell or tissue culture.

34. Use of a stem cell in the manufacture of a cellular medicament for transplantation to a patient, which cellular medicament comprises stem cells or the progeny thereof which have an altered MHC phenotype resulting from stable attenuation of expression of one or more MHC genes by introduction of double stranded RNA (dsRNA) into the stem cells.

35. Use of the compositions of any of claims3-6 in the manufacture of a medicament for attenuating expression of one or more genes in vivo.

36. A method for reducing the susceptibility of host cells to infection by pathogen, comprising introducing a double stranded RNA (dsRNA) into said host cells in an amount sufficient to attenuate expression of one or more genes necessary for expression by said pathogen.

37. The method ofclaim 36, wherein the pathogen is a virus, and the dsRNA attenuates expression of a cellular surface protein necessary for infection of the host cell by the virus.

38. A non-human transgenic mammal having germline and/or somatic cells comprising a transgene encoding a double stranded RNA transcriptional produce that is processed to an short interfering double-stranded RNA (siRNA) species, wherein transcription of said transgene attenuates expression of an endogenous target gene in at least one cell-type of the animal.

39. The transgenic animal ofclaim 38, which is chimeric for said transgene.

40. The transgenic animal ofclaim 38, wherein said transgene is chromosomally incorporated.

41. The transgenic animal ofclaim 38, wherein the transgene transcribes separate complementary transcripts that anneal to form said siRNA, which siRNA does not produce a significant PKR-dependent response at concentrations effective for attenuating expression of the target gene.

42. The transgenic animal ofclaim 38, wherein the transgene transcribes a hairpin RNA that is processed to said siRNA.

43. A hairpin RNA comprising a first nucleotide sequence that hybridizes under stringent conditions to a nucleotide sequence of a target gene, and a second nucleotide sequence which is a complementary inverted repeat of said first nucleotide sequence and hybridizes to said first nucleotide sequence to form a hairpin structure, which hairpin RNA attenuates expression of said target gene and does not produce a significant PKR-dependent response at concentrations effective for attenuating expression of the target gene.

44. The hairpin RNA ofclaim 43, wherein the hairpin RNA is chemically synthesized.

45. The hairpin RNA ofclaim 43, wherein the hairpin RNA is enzymatically synthesized in vitro.

46. The hairpin RNA ofclaim 45, wherein the hairpin RNA is synthesized by T7 RNA polymerase in vitro.

47. The hairpin RNA ofclaim 43, wherein the hairpin RNA is enzymatically synthesized in vivo.

48. The hairpin RNA ofclaim 47, wherein the hairpin RNA is synthesized by RNA polymerase III in vivo.

49. The hairpin RNA ofclaim 43, wherein the hairpin RNA is produced by a vector.

50. The hairpin RNA ofclaim 43, wherein the hairpin RNA has a size of about 20-50 nucleotides.

51. The hairpin RNA ofclaim 43, wherein the hairpin RNA has a size of about 50-100 nucleotides.

52. The hairpin RNA ofclaim 43, wherein the hairpin RNA has a size of about 100-500 nucleotides.

53. The hairpin RNA ofclaim 43, which includes a restriction enzyme site in the loop of the hairpin.

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