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.2016 May 26:6:26685.
doi: 10.1038/srep26685.

Optimization of CRISPR/Cas9 genome editing to modify abiotic stress responses in plants

Affiliations

Optimization of CRISPR/Cas9 genome editing to modify abiotic stress responses in plants

Yuriko Osakabe et al. Sci Rep..

Abstract

Genome editing using the CRISPR/Cas9 system can be used to modify plant genomes, however, improvements in specificity and applicability are still needed in order for the editing technique to be useful in various plant species. Here, using genome editing mediated by a truncated gRNA (tru-gRNA)/Cas9 combination, we generated new alleles for OST2, a proton pump in Arabidopsis, with no off-target effects. By following expression of Cas9 and the tru-gRNAs, newly generated mutations in CRIPSR/Cas9 transgenic plants were detected with high average mutation rates of up to 32.8% and no off-target effects using constitutive promoter. Reducing nuclear localization signals in Cas9 decreased the mutation rate. In contrast, tru-gRNA Cas9 cassettes driven by meristematic- and reproductive-tissue-specific promoters increased the heritable mutation rate in Arabidopsis, showing that high expression in the germ line can produce bi-allelic mutations. Finally, the new mutant alleles obtained for OST2 exhibited altered stomatal closing in response to environmental conditions. These results suggest further applications in molecular breeding to improve plant function using optimized plant CRISPR/Cas9 systems.

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Figures

Figure 1
Figure 1. Schematic illustrating the CRISPR/Cas9 vectors using truncated gRNAs, target sites in the Arabidopsis genes, and mutation detection.
(a) Schematic structure of the CRISPR/Cas9 vectors used in this study. The plant codon-optimized Cas9 with 3 × FLAG and 2 × NLSs was inserted in front of the 2A peptide fused with GBBSD2 under the control of the 2 × CaMV 35S promoter. The tru-gRNA can be inserted into theBsa I site and theAtU6-1 promoter was used in the expression cassette. Cas9 with a single NLS was also used to assess the effect of NLS number on mutation efficiency. The vectors were named pEgP526-2A-GFBSD2 and pEgP526-2A-GFBSD2 (Sp_SN), respectively. (b) Target sequences for mutagenesis with tru-RNA-guided genome editing in the Arabidopsis genome. The selected target sequences (17–18 b) for each gene are shown in black boxes and the PAM sequences are light blue boxes. Arrows; translational start sites (+1), Gray boxes; exons. (c) GFP fluorescence in the T1 transgenic plants of theOST2-CRISPR2 (pEgP526-2A-GFBSD2). Bar = 100 μm. (d) Cel-1 analysis of T1 transgenic plants ofGL1-CRISPR1 andOST2-CRISPR2 (pEgP526-2A-GFBSD2) and PCR-RFLP analysis ofABI4-CRISPR (pEgP526-2A-GFBSD2) with high GFP fluorescence compared with the wild-type control. Black arrows indicate the PCR products for wild-type sequence and yellow stars show the mutated bands digested with Cel-1 nuclease (GL1-CRISPR1 andOST2-CRISPR2) or undigested in PCR-RFLP (ABI4-CRISPR). L1, L2; individual T1 lines for transgenic plants. (e) Cel-1 analysis of T1 plants ofOST2-CRISPR2 transformed with the single NLS-Cas9 cassette {pEgP526-2A-GFBSD2 (Sp_SN)}. (f) Heteroduplex mobility assay (HMA) T1 plants transformed with the CRISPR/Cas9. Multiple heteroduplex peaks (blue triangles) were detected in PCR amplicons from each of the CRISPR/Cas9-transformed plants, whereas a single peak was detected from each wild-type control (black triangle).
Figure 2
Figure 2. Analysis of the mutated sequences induced by tru-gRNAs.
(a) Various types of CRISPR/Cas9-induced mutation detected by amplicon sequencing in T1 plants. The red boxes indicate target sites and green characters are PAM sequences. The blue characters show the nucleotide insertion. L1-7; the individual T1 lines for the transgenic plants. (b) The mutation rates analyzed by next-generation amplicon-based deep sequencing using mixed DNA pools from 15–30 GFP-positive T1 plants. (c) The detection ofsgRNA expression levels in individual T1 Arabidopsis plants with eachsgRNA specific primer with qRT-PCR. The value for one of the T1 lines of each construct was set to 1.0. To normalize the expression levels, 18S rRNA was amplified as an internal control. WT; wild-type Arabidopsis. (d) Protein blot analysis of GFP and Cas9 was performed with the individual T1 plants using an anti-GFP and Cas9 antibody, respectively. (e) The off-target mutation rates analyzed by next-generation amplicon-based deep sequencing using mixed DNA pools from 15–30 GFP-positive T1 plants. The off-target rates were shown by calculating the differences between these values and those from wild-type Arabidopsis (data not shown).
Figure 3
Figure 3. Generation of a new allele of the ost2 mutant using a tru-gRNA and Cas9 driven by a tissue-specific promoter, and the altered stomatal responses in Arabidopsis.
(a) Schematic structure of the CRISPR/Cas9 vectors harboring a tissue-specific promoter for Cas9 expression using Arabidopsiselongation factor α-1 (AtEF1) (pEgP126_Paef1-2A-GFPSD2) andhistoneH4 (AtH4) (pEgP126_Phis4-2A-GFPSD2) promoters. (b) GFP fluorescence in the T1 transgenic plants of the tissue-specific CRISPR/Cas9 vectors. Bar = 100 μm. (c) Generation of a new allele ofost2 mutant (ost2_crispr-1) using the tissue-specific CRISPR/Cas9. A base substitution (1492C to T, red character and asterisk in the sequence data) was detected in genomic DNA in the mutants. This mutation creates a stop codon (underlined) just after the mutation site. (d) A new mutant forOST2 gene (ost2_crispr-1) generated by the tissue-specific CRISPR/Cas9. Bar = 1 cm. (e) Thermal infrared imaging of the wild-type andost2_crispr-1 showing the temporal variability in stomatal conductance. (f ) Stomatal conductance of rossette leaves in the wild-type andost2_crispr-1 measured by leaf polometer. Values are means and SD (n = 20). Asterisks indicate statistically significant differences between the wild-type and mutant plants, determined by Student’st tests. *P < 0.0001 (g) Effects of various concentrations of ABA on stomatal closure inost2_crispr-1 and wild-type. Epidermal peels were treated with or without ABA for 1 h after stomatal preopening under light for 2 h, and the stomatal aperture was measured under a microscope. Values are means and SD (n = 30). Asterisks indicate statistically significant differences between the wild-type and mutant plants, determined by Student’st tests. *P < 0.0001. L1, L2 are T2 individuals harboring mutations in OST2 locus. (h) Transpirational water loss inost2_crispr-1 and wild-type at the indicated time points. Water loss is expressed as a percentage of the initial fresh weight. Values are means and SD of five samples of two shoots of eachost2_crispr-1 and wild-type.
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References

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