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Conservation of the sequence and temporal expression oflet-7 heterochronic regulatory RNA

Naturevolume 408pages86–89 (2000)Cite this article

Abstract

Two small RNAs regulate the timing ofCaenorhabditis elegans development1,2. Transition from the first to the second larval stage fates requires the 22-nucleotidelin-4 RNA1,3,4, and transition from late larval to adult cell fates requires the 21-nucleotidelet-7 RNA2. Thelin-4 andlet-7 RNA genes are not homologous to each other, but are each complementary to sequences in the 3′ untranslated regions of a set of protein-coding target genes that are normally negatively regulated by the RNAs1,2,5,6. Here we have detectedlet-7 RNAs of21 nucleotides in samples from a wide range of animal species, including vertebrate, ascidian, hemichordate, mollusc, annelid and arthropod, but not in RNAs from several cnidarian and poriferan species, Saccharomyces cerevisiae,Escherichia coli orArabidopsis. We did not detectlin-4 RNA in these species. We found thatlet-7 temporal regulation is also conserved:let-7 RNA expression is first detected at late larval stages inC. elegans andDrosophila, at 48 hours after fertilization in zebrafish, and in adult stages of annelids and molluscs. Thelet-7 regulatory RNA may control late temporal transitions during development across animal phylogeny.

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Figure 1:let-7 gene sequences.
Figure 2: Expression oflet-7 RNA in human andDrosophila.
Figure 3: Expression oflet-7 RNA is developmentally regulated in lophotrochozoans and deuterostomes.
Figure 4: Phylogenetic comparison oflet-7 RNA expression.

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References

  1. Lee, R. C., Feinbaum, R. L. & Ambros, V. TheC. elegans heterochronic genelin-4 encodes small RNAs with antisense complementarity tolin-14. Cell75, 843–854 ( 1993).

    Article CAS  Google Scholar 

  2. Reinhart, B. et al. The 21-nucleotidelet-7 RNA regulates developmental timing inC. elegans.Nature403, 901–906 (2000).

    Article CAS ADS  Google Scholar 

  3. Chalfie, M., Horvitz, H. R. & Sulston, J. E. Mutations that lead to reiterations in the cell lineages ofC. elegans.Cell24, 59– 69 (1981).

    Article CAS  Google Scholar 

  4. Ambros, V. & Horvitz, H. R. Thelin-14 locus of Caenorhabditis elegans controls the time of expression of specific postembryonic developmental events.Genes Dev.1, 398– 414 (1987).

    Article CAS  Google Scholar 

  5. Wightman, B., Ha, I. & Ruvkun, G. Posttranscriptional regulation of the heterochronic genelin-14 by lin-4 mediates temporal pattern formation inC. elegans. Cell75, 855–862 ( 1993).

    Article CAS  Google Scholar 

  6. Slack, F.et al. Thelin-41 RBCC gene acts in theC. elegans heterochronic pathway between thelet-7 regulatory RNA and the LIN-29 transcription factor.Mol. Cell5, 659– 669 (2000).

    Article CAS  Google Scholar 

  7. Aguinaldo, A. M. et al. Evidence for a clade of nematodes, arthropods and other moulting animals.Nature387, 489– 493 (1997).

    Article CAS  Google Scholar 

  8. Zamore, P. D., Tuschl, T., Sharp, P. A. & Bartel, D. P. RNAi: double-stranded RNA directs the ATP-dependent cleavage of mRNA at 21 to 23 nucleotide intervals.Cell101, 25–33 (2000).

    Article CAS  Google Scholar 

  9. Hammond, S. M., Bernstein, E., Beach, D. & Hannon, G. J. An RNA-directed nuclease mediates post-transcriptional gene silencing inDrosophila cells.Nature404, 293– 296 (2000).

    Article CAS ADS  Google Scholar 

  10. Tuschl, T., Zamore, P. D., Lehmann, R., Bartel, D. P. & Sharp, P. A. Targeted mRNA degradation by double-stranded RNAin vitro.Genes Dev.13, 3191 –3197 (1999).

    Article CAS  Google Scholar 

  11. Montgomery, M. K., Xu, S. & Fire, A. RNA as a target of double-stranded RNA-mediated genetic interference in Caenorhabiditis elegans.Proc. Natl Acad. Sci. USA 95, 15502–15507 (1998).

    Article CAS ADS  Google Scholar 

  12. Fire, A.et al. Potent and specific genetic interference by double-stranded RNA inCaenorhbditis elegans.Nature391, 806–810 (1998).

    Article CAS ADS  Google Scholar 

  13. Olsen, P. H. & Ambros, V. The lin-4 regulatory RNA controls developmental timing inCaenorhabditis elegans by blocking LIN-14 protein synthesis after the initiation of translation.Dev. Biol. 216, 671–680 (1999).

    Article CAS  Google Scholar 

  14. Tabara, H. et al. The rde-1 gene, RNA interference, and transposon silencing inC. elegans.Cell99, 123– 132 (1999).

    Article CAS  Google Scholar 

Download references

Acknowledgements

We thank the following people for RNA and tissue samples: T. Heanue, R. Pearse and C. Tabin for chick; J. Gerhart and M. Kirschner forXenopus and acorn worm; S. Agarwal forXenopus; N. Stavropoulos for mouse; C. Unabia and K. del Carmen for annelid and mollusc; H. Bode for Hydra; J. Nardone and S. Ferrari forArabidopsis; P. Sudarsanam for yeast; and D. Selinger forE. coli. The phylogenetic survey in this work was inspired by the NASA Evolution and Development meetings organized by E. Davidson and C. Golden. This work was supported by an NIH grant from NIGMS to G.R. and a grant from the MGH Fund for Medical Discovery to A.E.P.

Author information

Author notes
  1. Amy E. Pasquinelli, Brenda J. Reinhart, Patrick Leahy and Eric Davidson: These authors contributed equally to this work

Authors and Affiliations

  1. Department of Molecular Biology Massachusetts General Hospital, and Department of Genetics, Harvard Medical School, Boston, 02114, Massachusetts, USA

    Amy E. Pasquinelli, Brenda J. Reinhart & Gary Ruvkun

  2. Department of Molecular, Cellular and Developmental Biology, Yale University, New Haven, 06520, Connecticut, USA

    Frank Slack & Betsy Maller

  3. Kewalo Marine Lab, Pacific Biomedical Research Center, University of Hawaii, Honolulu, 96813, Hawaii , USA

    Mark Q. Martindale

  4. Howard Hughes Medical Institute, Baylor College of Medicine, Houston, 77030, Texas, USA

    Mitzi I. Kuroda

  5. Research School of Biological Sciences, PO Box 475, Australian National University, Canberra, 2601, ACT, Australia

    David C. Hayward & Eldon E. Ball

  6. Department of Zoology and Entomology University of Queensland, Brisbane, 4072, Queensland, Australia

    Bernard Degnan

  7. Institute of Zoology, University of Basel, Basel, CH-4051, Switzerland

    Peter Müller & Jürg Spring

  8. Cardiovascular Research Center, Massachusetts General Hospital, Charlestown, Massachusetts, 02129, USA

    Ashok Srinivasan & Mark Fishman

  9. Department of Biology, Boston University, Boston, 02215, Massachusetts, USA

    John Finnerty

  10. Department of Molecular and Cell Biology, University of California, Berkeley, 94720, California , USA

    Joseph Corbo & Michael Levine

  11. Division of Biology 156-29, California Institute of Technology, Pasadena, 91125, California, USA

    Patrick Leahy & Eric Davidson

Authors
  1. Amy E. Pasquinelli
  2. Brenda J. Reinhart
  3. Frank Slack
  4. Mark Q. Martindale
  5. Mitzi I. Kuroda
  6. Betsy Maller
  7. David C. Hayward
  8. Eldon E. Ball
  9. Bernard Degnan
  10. Peter Müller
  11. Jürg Spring
  12. Ashok Srinivasan
  13. Mark Fishman
  14. John Finnerty
  15. Joseph Corbo
  16. Michael Levine
  17. Patrick Leahy
  18. Eric Davidson
  19. Gary Ruvkun

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Pasquinelli, A., Reinhart, B., Slack, F.et al. Conservation of the sequence and temporal expression oflet-7 heterochronic regulatory RNA.Nature408, 86–89 (2000). https://doi.org/10.1038/35040556

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