- Open Access
Egg cell-specific promoter-controlled CRISPR/Cas9 efficiently generates homozygous mutants for multiple target genes in Arabidopsis in a single generation
- Zhi-Ping Wang†1,
- Hui-Li Xing†1,
- Li Dong1,
- Hai-Yan Zhang1,
- Chun-Yan Han1,
- Xue-Chen Wang1 and
- Qi-Jun Chen1Email author
© Wang et al. 2015
- Received: 22 April 2015
- Accepted: 2 July 2015
- Published: 21 July 2015
Arabidopsis mutants produced by constitutive overexpression of the CRISPR/Cas9 genome editing system are usually mosaics in the T1 generation. In this study, we used egg cell-specific promoters to drive the expression of Cas9 and obtained non-mosaic T1 mutants for multiple target genes with high efficiency. Comparisons of 12 combinations of eight promoters and two terminators found that the efficiency of the egg cell-specific promoter-controlled CRISPR/Cas9 system depended on the presence of a suitable terminator, and the composite promoter generated by fusing two egg cell-specific promoters resulted in much higher efficiency of mutation in the T1 generation compared with the single promoters.
- Transgenic Line
- Triple Mutant
- Multiple Target Gene
- Fusion Promoter
- Mutation Efficiency
The large collections of Arabidopsis sequence-indexed T-DNA insertion mutants (over 325,000 lines) have played a critical role in direct investigations of gene function . However, two major obstacles limit the application of these collections for genome-wide phenomic screening. First, most lines are hemizygous for the insertion, and thus have required an extra genotyping step to identify homozygous plants for phenotyping. Second, no T-DNA insertion mutants are available for 12 % of genes, and 8 % of genes are only represented by a single allele . Additionally, dissecting the roles of gene family members with redundant functions and analyzing epistatic relationships in genetic pathways frequently require plants bearing mutations in multiple genes. One hindrance to producing multi-gene mutants using T-DNA insertion mutagenesis is that this method requires time-consuming and labor-intensive genetic crossing of single-mutant plants. Advances in the use of sequence-specific nucleases, including homing meganucleases, zinc finger nucleases (ZFNs), transcription activator–like effector nucleases (TALENs), and, most recently, the RNA-guided DNA endonuclease Cas9 from the bacterial adaptive immune system CRISPR (clustered regularly interspaced short palindromic repeats) have paved the way for the development of rapid, cost-effective ways to create new mutant populations and multi-gene mutants in plants [3–7].
The CRISPR/Cas9 system uses an engineered single guide RNA (sgRNA) to provide sequence specificity, and depends on the endonuclease activity of the sgRNA/Cas9 complex to produce double-strand breaks at genomic sites specified by sgRNAs [7–10]; these double-strand breaks cause the activation of the DNA repair system in host cells, usually via the non-homologous end-joining pathway . Since the repair pathway is error-prone, small deletions or insertions will be introduced during the repair process, thus producing mutations . This highly efficient, easy-to-use system can potentially be used to make highly multiplexed genome modifications, and is supplanting the use of ZFNs and TALENs to become the standard genome-editing technology [3, 4, 6, 7]. In vertebrates, coinjection of in vitro transcribed Cas9 mRNA and sgRNA into single-cell embryos can produce multi-gene, biallelic mutant animals with high efficiency; the multiple mutations can also be efficiently transmitted to the next generation [11–16]. In plants, however, the presence of the cell wall makes methods using RNA injection impractical. Creating transgenic lines expressing the CRISPR/Cas9 system provides an alternative method [17–44].
Agrobacterium-mediated techniques used to create transgenic plant lines include in planta transformation and embryogenic callus-based transformation. The most typical example of in planta transformation is Agrobacterium-mediated transformation of Arabidopsis, whose egg cell is the target of the T-DNA [45–48]. Embryogenic cell-derived transgenic lines expressing the CRISPR/Cas9 system can be homozygous for edited target genes in the first generation, indicating that the target genes were edited in the transformed embryogenic cells before the first cell division . Similar results were reported in tomato  and maize . These results are encouraging for the development of crop genome editing, since crop transformation usually uses embryogenic callus cells, which can be considered to be analogous to animal embryos at the one-cell stage. In Arabidopsis, which is highly amenable to in planta transformation, the CRISPR/Cas9 system should theoretically be able to function in one-cell stage embryos. However, transgenic lines expressing CRISPR/Cas9 have mainly been mosaic in the first generation (T1), indicating that CRISPR/Cas9-induced mutations in Arabidopsis occurred after the first embryonic cell division [20, 22, 25, 26, 29, 35]. Perhaps the failure of CRISPR/Cas9 to function in one-cell stage embryos was due to the weak activity of the constitutive Cauliflower Mosaic Virus 35S promoter (CaMV 35S) in egg cells and one-cell stage embryos.
In this study, we used the promoter of the egg cell-specific EC1.2 gene [49, 50] to drive the expression of Cas9 in Arabidopsis, demonstrating that the specific expression of CRISPR/Cas9 in egg cells and one-cell stage embryos could efficiently lead to the creation of homozygous or biallelic mutants for multiple target genes in Arabidopsis in the T1 generation. Identification of completely mutated, non-mosaic lines will usually require medium-depth sequencing of target loci in a few candidate lines screened from 25–50 T1 transgenic plants via restriction enzyme digestion analysis, T7E1 assay, or Surveyor assay. However, the present strategy could shorten the time required to produce such mutants to a single generation, thus providing a quicker, more cost-effective means of creating new mutant populations and multi-gene mutants in Arabidopsis. Based on comparisons of different combinations of promoters and terminators, we also present a route to optimize the egg cell-specific promoter-controlled (EPC) CRISPR/Cas9 system.
Targeted mutations of multiple Arabidopsis genes in the T1 generation
Two reports have demonstrated that DD45/EC1.2 (At2g21740) is an egg cell-specific gene [49, 50]. In situ hybridization of tissue sections revealed that EC1.2 transcripts are specifically present in the egg cell, whereas GUS activity and GFP signals were observed in EC1.2p:GUS and EC1.2p:GFP transgenic zygotes and early embryos; the carryover of the signal into later stages of embryogenesis likely resulted from higher stability of the reporter mRNA and/or protein [49, 50]. We reasoned that Cas9 driven by the EC1.2 promoter would be specifically transcribed in the egg cell; Cas9 mRNA would reside in one-cell stage embryos due to mRNA stability and continue to translate Cas9 protein. Also, newly translated Cas9, together with residual Cas9 that remained due to Cas9 protein stability, would function in one-cell stage embryos, thus allowing creation of Arabidopsis T1 homozygous or biallelic mutants, rather than mosaic plants.
Mutation analysis of three T1 likely triple mutants and their T2 progeny
+T (×13)/−G (×11)
Phenotypic segregation analysis of T2 transgenic lines
20/20 (100 %)
11/34 (32.4 %)
33/156 (21.2 %)
20/20 (100 %)
27/49 (55.1 %)
42/98 (42.9 %)
15/47 (31.9 %)
18/45 (40.0 %)
25/77 (32.5 %)
13/64 (20.3 %)
57/94 (60.6 %)
53/90 (58.9 %)
To examine the specificity of the mutagenesis, we searched the Arabidopsis genome for potential off-targets with fewer than four mismatches with the targets of the sgRNAs. This identified three potential off-targets of the sgRNA targeting ETC2 . We sequenced these regions in the two triple mutants and found no mutations, demonstrating the high specificity of the EPC CRISPR/Cas9 system.
To confirm the repeatability of the results from EC1.2p:zCas9-rbcS_E9t transgenic lines, we performed two additional, independent Arabidopsis transformation experiments with the construct pHEE2A-TRI. In the second transformation, we obtained 41 T1 lines, among which three were likely triple mutants (Additional file 1: Figure S1). In the third transformation, we obtained 43 T1 lines, including four that were likely triple mutants (Additional file 1: Figure S2). Therefore, approximately 8.3 % (9/108) of the T1 plants were likely homozygous triple mutants.
We also demonstrated the usefulness of the EPC CRISPR/Cas9 system by performing targeted mutation of two Arabidopsis genes, CHLI1 and CHLI2, in T1 plants. Simultaneous disruption of CHLI1 and CHLI2 leads to an albino phenotype. We obtained 99 T1 lines, including 18 putative chli1 chli2 double mutants (albino plants, see Additional file 1: Figure S3). We sequenced the regions surrounding the target sites, and found that 10 lines were double mutants and five were mosaic plants (Additional file 2: Table S1). These results indicate that the EPC CRISPR/Cas9 was functional, not only in one-cell stage embryos, but also in some early embryos, likely due to Cas9 mRNA and/or protein stability, and/or reduced egg cell-specificity. Among the 18 albino lines, three grew poorly, and we were unable to obtain sequence data from these lines (Additional file 1: Figure S3, Additional file 2: Table S1). These three albinos were most likely double mutants rather than mosaics, based on their poor growth. Thus, the ratio of homozygous T1 double mutants to T1 plants was approximately 13 % (13/99). Together, these results demonstrate that our EPC CRISPR/Cas9 system could be used to efficiently produce confirmed T1 homozygous or biallelic mutants in less than 3 months (Additional file 3: Figure S4). In practical applications, users might have no visible phenotypes that they could use to screen for T1 homozygous mutants. However, this obstacle can be easily overcome by screening 25–50 T1 lines by restriction enzyme digestion analysis, T7E1 assay, or Surveyor assay (Additional file 3: Figure S5). After these primary screens, users will be able to quickly obtain a few candidate lines for sequence analysis (including direct sequencing of PCR fragments, sequencing individual clones of PCR fragments, and deep sequencing of PCR fragments) (Additional file 3: Figure S5).
To confirm that the T1 mutations are germline transmissible, we sowed 20 T2 seeds per T1 line derived from the two T1 triple mutant lines (#1 and #3) on MS plates. We observed no phenotypic segregation of these T2 plants (Table 2). Moreover, sequencing analysis of four T2 plants per T1 line showed no novel mutation types (Table 1). These results strongly suggested that germline transmission of T1 mutations occurred. To further confirm the germline transmission of the T1 mutations, we screened for non-transgenic T2 lines and analyzed their mutations. Since we harvested <30 T2 seeds per T1 line from the two triple mutant T1 lines (#1 and #3) due to their poor growth, no additional T2 seeds were available for screening of non-transgenic lines. We then turned to screening for non-transgenic T2 plants derived from the T1 triple mutant (#C1) produced in the third transformation (Additional file 1: Figure S2). We sowed 36 T2 seeds on MS plates, and transplanted the seedlings to soil. All 36 T2 plants were phenotypically triple mutants. We screened all 36 T2 plants for non-transgenic plants and obtained only one such plant, much fewer than the nine or so plants we expected, which may reflect insertions of two or more copies of T-DNAs into the genome of the T1 plant. We analyzed the mutations of the T1 mutant (#C1) and the non-transgenic T2 mutant (#C1-17) by sequencing (Table 1), which demonstrated that the T2 mutations are derived from the originally confirmed, rather than newly produced, T1 mutations through germline transmission (Table 1).
Analysis of mutations in the phenotypically wild-type T1 plants and their T2 progeny
Mutation analysis of likely triple mutants segregated from two representative T1 lines with normal phenotypes
+G (×3)//+A (×9)//−G (×7)//+C (×2)
−8 (×8)/−G + T (×2)
+T (×9)/+5 (×11)
+A (×7)/−5 (×3)
+G (×4)/−14 + 4 (×6)
−41 (×9)/−24 (×11)
−14 + A (×13)/+A (×7)
+G (×8)/−G (×2)
−G (×7)/−8 (×3)
+T (×3)/−G (×7)
0 (×13)//+G (×2)//+A (×1)//+T (×2)
+A (×2)//−5 (×1)//−41 (×2)//−52 + 9 (×3)//−24 (×2)
0 (×4)//+G (×5)//−G (×8)//−22 + 16 (×5)
−52 + 9/−52 + 9
−22 + 16(×6)/−3(×5)
0 (×7)//+T (×1)//+A (×1)
−G (×10)//+G (×5)//−26 (×4)
0 (×15)//+A (×2)//+T (×1)//−14 + 4 (×1)//−11 (×2)
eetxcx or eettcx
−52 + 9/−52 + 9
+T (×5)//+G (×3)//−G (×2)//−22 + 16 (×3)
+A (×5)/+A (×5)
eetxcc or eettcc
−52 + 9/−52 + 9
−22 + 16/−22 + 16
−52 + 9/−52 + 9
−22 + 16 (×5)/+G (×3)
−41 (×5)//−24 (×3)//−30 + 17 (×2)//+A (×2)
−G (×8)//+G (×2)//−22 + 16 (×1)
+A (×1)/+T (×8)
extxcc or eettcc
−4 (×16)/+G (×4)
−G (×9)/+C (×2)
+C (×10)/−49 (×10)
−52 + 9/−52 + 9
+A (×5)//−G (×2)//−22 + 16 (×1)
eetxcc or eettcc
Functional comparisons of 12 combinations of eight promoters and two terminators
In our previous work, we demonstrated that constitutive overexpression of zCas9 driven by the double 35S promoter in T1 2x35Sp:zCas9-Nost transgenic lines (using construct p2gR-TRI-A, renamed pHSN2A-TRI in this paper) efficiently produced mutations for TRY, CPC, and ETC2, but all the mutants were mosaics . Since EC1p/rbcS-E9t combinations (pHEE2A-TRI and pHEE2B-TRI) performed much better than EC1p/Nost combinations (pHEN2A-TRI, pHEN2B-TRI, and pHEN2C-TRI), we reasoned that the 2x35Sp/rbcS-E9t combination (pHSE2A-TRI) would perform much better than the 2x35Sp/Nost combination (pHSN2A-TRI). We constructed pHSE2A-TRI (Fig. 3a), and obtained 109 T1 2x35Sp:zCas9-rbcS_E9t transgenic lines. None of the T1 lines are likely triple mutants (Fig. 3a), demonstrating again that almost all mutants produced from the T1 2x35S:Cas9 transgenic lines are mosaics. The ratios of mutants from T1 2x35Sp:zCas9-rbcS_E9t lines with strong (30.3 %) or observable (68.8 %) phenotypes to total number of T1 lines are much lower than those from T1 2x35Sp:zCas9-Nost lines (78.8 % and 97.0 %, respectively). These results demonstrated that 2x35Sp/rbcS-E9t combination did not perform much better than 2x35Sp/Nost combination, suggesting that in vegetative cells, the nos terminator seemed to work better than the rbcS-E9 terminator. Considering statistical errors (for example, due to insufficient sample population for 2x35Sp:zCas9-Nost transgenic lines), another possibility is that zCas9 mRNA stability is not as important for strong constitutive promoters as it is for egg cell-specific promoters.
To determine whether the 35S enhancer could increase the expression driven by the egg cell-specific promoters, we constructed three fusion promoters by fusing the 35S enhancer with the egg cell-specific promoters and then generated transgenic lines for the analysis of these fusion promoters’ activities (Fig. 3b). The ratio (26/67, 38.8 %) of 35Sen-EC1.1p:zCas9 plants with observable mutations to the total number of T1 transgenic lines was much higher than that (32/224, 14.3 %) of EC1.1p:zCas9-rbcS_E9t plants with observable mutations (Fig. 3b). In comparison with the ratio for T1 EC1.2p:zCas9-rbcS_E9t transgenic lines, the ratios of plants with observable mutations to total numbers of T1 35Sen-EC1.2p(900-bp):zCas9 or 35Sen-EC1.2p(565-bp):zCas9 transgenic lines greatly increased – 11.1 % (12/108), 25.2 % (29/115), and 29.0 % (20/69) for the three transgenic lines, respectively – whereas the ratios of likely triple mutants decreased (8.3 %, 3.5 %, and 1.4 % for the three transgenic lines, respectively) (Fig. 3b). These results demonstrated that the CaMV 35S enhancer increased the expression of EC1.1 or EC1.2 promoters but not in an egg cell-specific way. Thus, the CaMV 35S enhancer is not suitable for improving the EPC CRISPR/Cas9 system, which is consistent with our notion that the CaMV 35S promoter has weak activity in egg cells and one-cell stage embryos.
To determine whether the enhancer from the EC1.2 promoter or EASE  could improve the performance of the EPC CRISPR/Cas9 system, we constructed another two fusion promoters by fusing the enhancer from the EC1.2 promoter (EC1.2en), or EC1.2en plus double EASE enhancers (EC1.2en-2xEASE), with the EC1.1 promoter (Fig. 3b). The ratio (17.0 %) of EC1.2en-EC1.1p:zCas9-rbcS_E9t plant-derived likely triple mutants to total number of T1 transgenic lines greatly increased (Fig. 3b, Additional file 4: Figure S8) in comparison with those for the EC1.2p/EC1.1p:zCas9-rbcS_E9t plant-derived mutants (8.3 % and 1.8 %, respectively, Fig. 3a). The ratio (28.3 %) of EC1.2en-EC1.1p:zCas9-rbcS_E9t plants with observable mutations to total number of T1 transgenic lines also greatly increased (Fig. 3b, Additional file 4: Figure S8) in comparison with those for the EC1.2p/EC1.1p:zCas9-rbcS_E9t plants with observable mutations (11.1 % and 14.3 %, respectively, Fig. 3a). These results demonstrated that the EC1.2en-EC1.1p fusion promoter performed much better than the single EC1.2 or EC1.1 promoters, and the enhancer from the EC1.2 promoter significantly improved egg cell-specificity and expression strength of EC1.1 promoter. Unexpectedly, when we added double EASE enhancers into the EC1.2en-EC1.1p fusion promoter, the resultant fusion promoter caused lower mutation efficiency: only 8.3 % (10/120) EC1.2en-2xEASE-EC1.1p:zCas9-rbcS_E9t plants harbor the observable mutations (Fig. 3b, Additional file 4: Figure S9). These results suggested that EC1 and EASE have different mechanisms for egg cell-specific expression, and the two mechanisms seem to be antagonistic.
For most plants, including crops, genetic transformation is usually performed with embryogenic callus cells induced during tissue culture. Recent studies have demonstrated that embryogenic cell-derived transgenic lines expressing the CRISPR/Cas9 system could be homozygous mutant for edited target genes in the first generation [26–28, 33]. For Arabidopsis, the only plant species currently compatible with efficient, in planta transformation, most modifications detected in first-generation CRISPR/Cas9 transgenic lines were only somatic mutations [20, 25, 26, 29, 30, 34, 35]. Therefore it was proposed that screening of heritable mutations should be performed in the T2 or subsequent generations . However, we reasoned that the excess of mosaic plants and lack of homozygous mutants was probably due to the low expression level of Cas9 driven by constitutive promoters (usually the 35S promoter) in egg cells and one-cell stage embryos. Due to the stability of Cas9 mRNA and Cas9 protein, CRISPR/Cas9 specifically expressed in egg cells should function in one-cell embryos, allowing the creation of homozygous or bi-allelic T1 mutants. Consistent with this notion, in the current study, we used an egg cell-specific promoter to express Cas9 and succeeded in creating T1 homozygous (or bi-allelic) mutants harboring two or three target genes that were modified simultaneously. More importantly, since approximately 8.3 % and 13.1 % of T1 plants are non-mosaic triple and double mutants for the representative three and two target genes, respectively, we demonstrated that mutation efficiencies of the system would be sufficient for producing customized Arabidopsis mutants. Although some mosaics still formed in T1 and T2 plants due to Cas9 mRNA and/or protein stability (Table 3, Additional file 2: Tables S1 and S2), these mosaics were derived from early embryos (probably two- or four-celled embryos) and were thus stable in terms of the types and patterns of mutations (Additional file 2: Table S2). Therefore, some mosaic plants harboring more than two mutant alleles but lacking wild-type alleles are equivalent to homozygous (or bi-allelic) mutants in phenotypes or gene-specific traits. By contrast, the mutation types and patterns of the mosaic plants resulting from 35Sp:Cas9 transformation were usually unstable and variable throughout development and in different tissues or organs. So, even if some mosaics would be unavoidable to be produced from EC1.2p:Cas9, these mosaics could produce much higher ratios of homozygous (or bi-allelic) mutant progeny harboring much more highly predictable mutation types than mosaics from 35S:Cas9 could do. Therefore, the mosaics, if unavoidable, from EC1.2p:Cas9 or EC1.2en-EC1.1p:Cas9 are more useful for screening for homozygous mutant progeny, especially non-transgenic homozygous mutants in T2 generation, than those from 35S:Cas9 are (Additional file 3: Figure S4).
Ma et al.  recently reported that using 2x35Sp:Cas9p they obtained about 8.5 % non-mosaic T1 mutations (10 out of 118 sequenced target sites). Since these sequenced target sites involved six target sites in four genes (three targets in the same gene and three targets in three other genes) of about 100 T1 lines, this means that they obtained approximately 9.0 % (9/100) non-mosaic T1 mutants. They obtained one T1 mutant, out of 14 T1 lines, with non-mosaic, simultaneous mutations of two target sites of the same gene. However, they failed to obtain the mutants (0/14) with simultaneous mutations of three target sites. These results suggest that 2x35Sp:Cas9 transgenic lines have much lower mutation efficiencies for the generation of T1 homozygous or biallelic mutants for multiple target genes than EC1.2p:Cas9 transgenic lines, which is consistent with our results.
In this study, to evaluate mutation efficiencies and determine the size of the T1 population needed for screening for homozygous mutants, we used screenable phenotypes for the identification of the triple or double mutants. In practical applications, the genes-of-interest might have no convenient, visible phenotype. One potential, low-cost strategy for identifying mutants is to select, as far as possible, targets with cleavage sites located within restriction enzyme sites. In this case, users can conduct primary screening by restriction enzyme digestion analysis (Additional file 3: Figure S5), as the occurrence of a mutation should disrupt the restriction enzyme site . Alternatively, users could conduct primary screening by T7E1 or Surveyor assay [8, 22]. Then, users can perform sequencing analysis, based on three strategies, of primarily screened lines that likely are bi-allelic mutants (Additional file 3: Figure S5). One strategy is direct sequencing purified PCR fragments spanning target sites using primers within PCR fragments. For homozygous (or bi-allelic) mutations with a one base pair insertion or deletion, this strategy would work well. Sequencing of individual clones of PCR fragments and deep sequencing of PCR fragments can also be used to identify non-mosaic, mutant plants. However, the high frequencies of mutations induced by this method will also allow users to identify non-mosaic mutants by using the simplest and most effective (but also expensive) method, deep sequencing of PCR fragments spanning target sites from 25–50 T1 transgenic lines.
Some targets may have much lower mutation efficiencies than others, so we suggest selecting three sets of targets, with two sets as backups to avoid being delayed by possibly recalcitrant targets (Additional file 3: Figure S5). Construction of a binary vector harboring two sgRNAs is very simple and only a single additional PCR fragment is required for the cloning system . Therefore, even for targeted mutation of a single gene, we suggest always constructing a binary vector that harbors two sgRNAs targeting two sites in the same gene. Thus, with two backup vectors, this method provides sextuple assurance of getting targeted mutations of a single gene.
A critical finding in this study is that one of the key factors determining our success with the EPC CRISPR/Cas9 system was the presence of a suitable terminator. T1 and T2 plants with observable mutations (including likely triple/double mutants and mosaics) were infrequent when these plants were derived from EC1.2p:zCas9-Nost transgenic lines, which used the nos terminator. By contrast, an average of 24.8 % T2 plants derived from EC1.2p:zCas9-rbcS_E9t, which used the rbcS-E9 terminator, were likely triple mutants (Table 2). Indeed, while the use of the same promoter with different terminators has been shown to sometimes result in significantly different levels of protein accumulation , the large difference in mutation efficiencies observed between the two terminators in the current study was unexpected. Comparison of mutation frequencies of additional constructs (pHEE2B-TRI and pHEN2B-TRI, or pHEE2A-TRI and pHEN2C-TRI) provided additional proof that the rbcS E9 terminator performed much better than the nos terminator (Fig. 3). These results suggest that the presence of the proper terminator is a key factor in stabilizing Cas9 mRNA in egg cells, and different terminators have significantly different effects on Cas9 mRNA stability.
CRISPR/Cas9-based multiplex genome editing requires multiple sgRNAs and maintaining appropriate concentrations of each variant of sgRNA-Cas9 complex in a cell for target search according to the target recognition mechanism . Since methods have been developed to assemble multiple sgRNAs [26, 37, 54, 56, 57], highly efficient expression of multiple sgRNAs in a cell has not been a problem. However, co-existence of multiple sgRNAs in a cell would dilute the concentration of each variant of the sgRNA-Cas9 complex harboring a specific target sequence. Thus, although the total concentration of all sgRNA-Cas9 complexes may remain stable, the functional concentration of each variant of the sgRNA-Cas9 complex would decrease in inverse proportion to the numbers of sgRNA variants or target sites. Thus, it is important to express Cas9 more efficiently to increase the concentration of each variant of the sgRNA-Cas9 complex and thus enhance the efficiency of multiplex genome editing. Consistent with this notion, our results demonstrated that mutation efficiencies for multiple targets could be greatly increased by using not only appropriate promoters to drive the expression of Cas9 but also appropriate terminators to stabilize Cas9 mRNA. These observations should facilitate development or improvement of genome editing methods for the generation of non-mosaic mutants for multiple target genes in other organisms, especially through specific expression of CRISPR/Cas9 in germline cells, gametes, or one-cell stage embryos . Although currently Arabidopsis is the only species amenable to in planta transformation method with high efficiency, along with the development of in planta transformation for other plants, it is possible that the egg cell-specific promoter-controlled CRISPR/Cas9 system or similar strategies will be very useful for more plant species.
Localized egg-cell expression of a ZFN was previously employed for targeted editing of the Arabidopsis genome . In this case, the EASE:QQR-ZFN expression cassette was used; EASE is an enhancer sequence that specifically regulates gene expression in the egg apparatus of Arabidopsis, and QQR-ZFN is a well-characterized ZFN that functions in planta [53, 59]. However, the reported mutation frequencies were not high enough for practical application. No mutations were detected in T1 EASE:QQR-ZFN plants, and the mutation frequency of T2 plants was only 0.078 % (7/9000) in a GUS staining assay and only 0.27 % (1/366) in a PCR-based assay. Even if the actual mutation rate were underestimated, the mutation frequency of T2 plants was not much higher than 0.5 % for the single target gene. By contrast, in our EC1.2p:Cas9-based system, approximately 8.3 % of the T1 plants and an average of 24.8 % of the T2 plants were likely triple mutants (Table 3). These results might reflect the differences between CRISPR/Cas9 and ZFN, between EC1.2p and EASE, and/or between the terminators used in the two cassettes.
Although the mutation efficiencies that can be obtained using the EC1.2 promoter-controlled CRISPR/Cas9 system are high enough to allow researchers to customize their own Arabidopsis mutants, higher target gene editing efficiencies can be anticipated. As an example, the fusion promoter from two egg cell-specific genes EC1.2 and EC1.1 resulted in much higher efficiency of mutation compared with the single promoters. By fusing more enhancers from the EC1 genes (including EC1.1–EC1.5) to the EC1.1 or EC1.2 promoter , stronger and more specific expression of Cas9 in egg cells and one-cell stage embryos could be anticipated. In addition, by using more effective terminators than rbcS E9 terminator, the EPC CRISPR/Cas9 system could be further improved. The optimized combinations of fusion promoters and terminators will greatly enhance the mutation efficiencies. It has been shown that, after transfection by Agrobacterium, the ratio (7 %) of ovules demonstrating transient expression to total number of ovules examined was much higher than ratio (0.44 %) of ovules developing into stable transgenic seeds to total number of ovules/seeds examined . Thus, this enhanced system would allow us to create non-transgenic, gain-of-function T1 mutants via homologous recombination mediated by the EPC CRISPR/Cas9 system, which is currently a formidable challenge . Finally, with the development of high-throughput sequencing, deep sequencing of large batches of PCR products will become affordable and the time required to identify targeted gene modifications will be further shortened.
Probing gene function and examining gene interactions requires the generation of single, double, and multiple mutants in different combinations. However, in plants, generation of these mutants requires screening of banks of existing mutants, followed by laborious and time-consuming crossing and screening for multiple mutants. New genome-editing methods, such as the CRISPR/Cas9 system, can be used to generate targeted gene modifications in Arabidopsis; however, almost all first-generation CRISPR/Cas9 transgenic Arabidopsis plants have been mosaic for the targeted genes. This study demonstrates that specifically expressing Cas9 in egg cells and one-cell stage embryos enables the creation of homozygous or biallelic T1 mutants for multiple target genes with high efficiency: 2 of 24 (8.3 %) of the T1 plants were homozygous or biallelic cpc try etc2 triple mutants. Moreover, 12 of the 24 T1 plants gave rise to homozygous triple mutants in the T2 generation. The segregation ratio of likely triple mutants to total T2 plants was over 20 % for all 12 T1 lines and averaged 24.8 % for all 24 T1 lines. We also generated chli1 chli2 homozygous or biallelic double mutants with a ratio of 13.1 % (13/99) in T1 generation. Comparisons of 12 combinations of eight promoters and two terminators found that the efficiency of the egg cell-specific promoter-controlled (EPC) CRISPR/Cas9 system depended on the presence of a suitable terminator, and the fusion promoter from two egg cell-specific genes EC1.2 and EC1.1 resulted in much higher efficiency of mutation in the T1 generation compared with the single promoters. This system provides a rapid, cost-effective way to create new mutant populations and multi-gene mutants in Arabidopsis. This study also presented a route to optimize the EPC CRISPR/Cas9 system.
Detailed descriptions of the vector construction are provided in Additional file 5: Methods S1. All primers used in this study are listed in Additional file 2: Table S3. The vector sequences are provided in Additional file 6.
Generation of transgenic Arabidopsis plants and analysis of mutations
We transformed the pHEE2A/B/D1/D2/D3/E/F-TRI, pHEN2C-TRI, pHSE2A-TRI, and pHEE2A-CHLI constructs into Agrobacterium strain GV3101, and transformed pHEN2A/B-TRI into GV3101/pSoup . We transformed Arabidopsis Col-0 wild-type plants via the floral dip method . We screened the collected seeds from the T0 plants on MS plates containing 25 mg/L hygromycin, and transplanted the resistant seedlings (T1) to soil. We extracted genomic DNA from T1 transgenic plants grown in soil. To analyze mutations of TRY, CPC, and ETC2, we amplified fragments surrounding the target sites of TRY, CPC, or ETC2 by PCR using gene-specific primers TRY-IDF0/R0, CPC-IDF0/R0, or ETC2-IDF0/R0, respectively . We submitted purified PCR products for direct sequencing with primers TRY/CPC/ETC2-seqF  located within the PCR fragments. To analyze possible mutations of potential off-target sites of TRY, CPC, and AT5G50230 of the sgRNA targeting ETC2, we amplified fragments surrounding the off-target sites by PCR using gene-specific primers TRY-off-IDF/R, CPC-off-IDF2/R, or 5G50230-off-IDF/R, respectively. We submitted purified PCR products for direct sequencing (as opposed to sequencing of individual clones of PCR products) with primers TRY/CPC/5G50230-off-seqF located within the PCR fragments. To analyze mutations of CHLI1 and CHLI2, we amplified fragments surrounding the target sites of CHLI1 or CHLI2 by PCR using gene-specific primers CHLI1-IDF/R or CHLI2-IDF/R, respectively. We submitted purified PCR products for direct sequencing with primers CHLI1/2-seqF located within the PCR fragments. We then cloned poorly sequenced PCR products, and submitted individual positive clones for sequencing using the T7 primer. To screen the segregated non-transgenic T2 plants, we first screened nine primer combinations, with three forward primers including zCas9-IDF3-2/-IDF5/-IDF6 (located at zCas9) and three reverse primers including rbcS_E9t-IDR/-IDR2 (located at rbcS-E9 terminator) and lacp-IDF (located at the lac promoter of the vector backbone), for more specific primers (Additional file 2: Table S3). We obtained three more specific primer pairs, including zCas9-IDF3-2/rbcS_E9t-IDR2, zCas9-IDF5/lacp-IDF, and zCas9-IDF6/lacp-IDF, with wild-type genomic DNA serving as a negative control and genomic DNA from T1 transgenic plants serving as a positive control (Additional file 2: Table S3). We then performed counterselection PCR with the three primer pairs for screening of non-transgenic T2 plants.
We would like to thank the scientists of Plant Editors Cooperative for editing our manuscript. This work was supported by grants from the National Science Foundation of China (31070329), the National Basic Research Program of China (2012CB114200), and the National Transgenic Research Project (2011ZX08009).
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