A simple and reliable method for creating PCR-detectable mutants in Arabidopsis with the polycistronic tRNA–gRNA CRISPR/Cas9 system
To develop an easy and robust method for creating genetically stable and easily detectable Arabidopsis mutants, we adopted the polycistronic tRNA–gRNA CRISPR/Cas9 (PTG/Cas9) system, a multiplex gene-editing tool in rice, with PTOX as the reporter gene. The PTG/Cas9 system has a great potential in generating large deletions detectable by PCR, which greatly simplifies the laborious work of mutant screening. We constructed a PTOX–PTG/Cas9 system with five gRNAs and introduced it into Arabidopsis. At T1 generation, 24.4% of transgenic plants were chimeric with PCR-detectable deletions in PTOX locus, but no homozygous mutant was found, indicating that gene editing occurred predominantly in somatic cells. After a self-cross propagation, 60% of T1 chimeric plants were able to produce homozygous, heterozygous, or bi-allelic ptox offsprings. Inheritable homozygous ptox mutants without Cas9 gene can be obtained earliest at T2 generation. We further targeted five other genes using the same procedure and achieved homozygous Cas9-free mutants with large deletions for all genes within three generations. We established a standard and reliable protocol to generate stable inherited deletion mutants in 2–3 generations along with simple PCR screening methods. We conclude that the rice PTG/Cas9 system is an efficient, easy, and rapid tool to edit genes in Arabidopsis. We propose that it could be applied to other genes in Arabidopsis, and it might have the potential to edit genes in other plant species as well.
KeywordsArabidopsis Gene editing Polycistronic tRNA–gRNA CRISPR/Cas9 system PTOX (plastid terminal oxidase) Cas9-free deletion mutant
Clustered regularly interspaced short palindromic repeat
CRISPR-associated nuclease 9
Protospacer adjacent motif
Plastid terminal oxidase
U3 snoRNA promoters
Collections of T-DNA insertional mutants have made vital contributions to determining functions of Arabidopsis genes. However, there are still 12% of Arabidopsis genes lacking T-DNA insertion and 8% genes with a single insertion in publically available T-DNA insertional mutant libraries (O’Malley and Ecker 2010; Kleinboelting et al. 2015, 2017). Moreover, T-DNA favors inserting into the regions of transcriptional initiation and polyadenylation, which usually results in a partial suppression of gene’s functions (Li et al. 2006). Therefore, there still is a large need to create gene knockout mutants in Arabidopsis; and gene-editing technologies provide powerful tools to fulfil this imperative requirement (Liu et al. 2013). Today, the RNA-guided nuclease complex, the clustered regularly interspaced short palindromic repeat (CRISPR)/CRISPR-associated nuclease 9 (Cas9), is the most powerful and widely used tool to edit genes in diverse organisms due to its high efficiency and great specificity (Jinek et al. 2012; Doudna and Charpentier 2014).
The CRISPR/Cas9 system is derived from the type II CRISPR adaptive immune system in Streptococcus pyogenes, which detects and degrades invasive DNAs from bacteriophages and plasmids (Jinek et al. 2012; Fineran and Charpentier 2012; Gasiunas et al. 2012). It consists of two components, an endonuclease Cas9 and a synthetic guide RNA (gRNA) harboring a 20-nt spacer and a 76-nt Cas9-binding scaffold. After being expressed in plants, Cas9 is introduced to the genomic site that is base-paired with the gRNA spacer, binds to its downstream protospacer adjacent motif (PAM) with a consensus sequence of NGG, and creates a double-strand break (DSB) at a site ~ 3 bp upstream of PAM (Jinek et al. 2012; Doudna and Charpentier 2014). Then, DSB is repaired through either an error-free homologous recombination mechanism or an error-prone non-homologous end-joining pathway. The latter process often leads to insertions, deletions, or substitutions at the target sites (Mali et al. 2013; Cong et al. 2013).
A number of CRISPR/Cas9 systems have been developed and successfully applied to edit genes in Arabidopsis (Ma et al. 2016; Ding et al. 2016; Liu et al. 2017). The early versions usually encode a single gRNA driven by a Pol III promoter and a Cas9 gene driven by the 35S promoter (Shan et al. 2013; Li et al. 2013; Nekrasov et al. 2013; Feng et al. 2013). However, the CRISPR/Cas9 system-directed gene-editing efficiency is much lower in Arabidopsis compared to other plant species, probably because the Arabidopsis gene transformation method does not require a tissue regeneration process, which is usually applied to most plant species. In addition, the generated mutations are often somatic and rarely transmitted to the next generation. Single gRNA CRISPR-Cas9 systems normally generate SNP or short indel mutations at target sites, which can be detected by time-consuming and laborious methods, like DNA sequencing or PCR–RFLP if the mutation destroys a restriction enzyme site. A number of advanced methods were developed to detect SNP or small indel events, including Indel Detection by Amplicon Analysis (IDAA, Yang et al. 2015), qPCR/dPCR (Mock et al. 2016; Falabella et al. 2017), amplicon next-generation sequencing (NGS, Sentmanat et al. 2018), inference of CRISPR edits (ICE, Hsiau et al. 2018), and tracking indels by decomposition (TIDE, Brinkman et al. 2018); however, they are quite expensive and require special equipment or sequencing.
In recent years, many efforts were made to increase the editing capacity and efficiency in Arabidopsis. One way is to promote the expression of Cas9 in stem cells using egg cell-specific promoters like the Yao or EC1.2 promoter instead of the constitutively expressing promoters like the 35S or ubiquitin promoter, leading to an increase of the inheritable mutation rate (Yan et al. 2015; Wang et al. 2015). The other way is to raise the number of genomic target sites by expressing multiple gRNAs simultaneously in plants. Multiplex gene-editing systems could be constructed by assembling several independent gRNA expression cassettes in one vector (Ma et al. 2015; Zhang et al. 2016), or by compacting multiple gRNAs into a single expression cassette and recruiting endogenous post-transcriptional RNA processing systems to generate multiple gRNAs (Gao and Zhao 2014; Nissim et al. 2014; Xie et al. 2015). Multiplex gene-editing systems are not only able to increase the editing efficiency, but also can simplify the mutation identification, because they are capable of generating large PCR-detectable deletions between two target sites. Therefore, using multiplex gene-editing systems followed by a PCR examination on large deletion events, we are able to develop an efficient method to robustly generate target mutants and boost the application of CRISPR/Cas9 systems in Arabidopsis.
The polycistronic tRNA–gRNA (PTG)/Cas9 system originally developed for rice is a powerful multiplex gene-editing system with a frequency of up to ~ 100% (Xie et al. 2015). It clusters multiple tRNA–gRNA architectures into one expression cassette, designated as PTG gene, each gRNA carrying a different spacer sequence. Through plant endogenous tRNA-processing system, tRNA fragments are excised out from the primary transcripts of the PTG gene, releasing all the gRNAs to guide gene editing (Xie et al. 2015). This system has been successfully used in maize (Qi et al. 2016) and kiwifruit (Wang et al. 2018) after some modifications like switching the rice tRNA or promoters to corresponding elements from the host plant species. Compared to other multiplex gene-editing systems, the PTG/Cas9 system is relatively easier in vector construction and transformation, especially when the number of gRNAs increases (Ma et al. 2015; Zhang et al. 2016).
The rice PTG/Cas9 system could also work in Arabidopsis, since all components essential for this system are conserved in plants (Xie et al. 2015). In this work, we applied this rice PTG/Cas9 in Arabidopsis for several genes, and it was indeed able to create large PCR-detectable deletions at desired loci. Based on this property, we were able to identify and isolate stably heritable Arabidopsis Cas9-free mutants in two or three generations through simple PCR screening. In addition, we summarized a reliable and standard protocol to generate and identify Arabidopsis deletion mutants using the rice PTG/Cas9 editing system and the PCR screening method.
Materials and methods
All the primers used in this experiment are listed in Table S1.
Plant materials and growth conditions
Arabidopsis thaliana wild-type Columbia-0 (Col-0), mutant im (At4g22260), and PTG/Cas9 transgenic plants in Col-0 background were planted in soil or half-strength MS (1/2MS) medium supplemented with 1% (w/v) sucrose. Seedlings were germinated and grown under low light condition (23 °C, 30 μmol m−2 s−1, 16-h light/8-h dark daylight cycle) for 10 days, and then transferred to the normal light condition (23 °C, 100 μmol m−2 s−1, 16-h light/8-h dark daylight cycle).
Constructing gene-specific PTG/Cas9 system
Fragment 1 with composition of (5′) FokI adaptor::tRNA::5′ half of gRNA1 spacer::BsaI (3′) was amplified using primers 5′L-F and gRNA1-R. The intermediate fragments were amplified with primers gRNA(n − 1)-F and gRNAn-R, generating a structure of (5′) BsaI::3′ half of gRNA(n − 1) spacer::gRNA scaffold::tRNA::5′ half of gRNAn spacer::BsaI (3′). The last fragment, fragment 6, was amplified with primers gRNA5-F and 3′L-R, resulting in the composition of (5′) BsaI::3′ half of gRNA5 spacer::gRNA scaffold::FokI adaptor (3′). The PCR reaction in this step was performed in a 50-μl mix containing 0.1-ng pGTR plasmid, 1 × Primer STAR Max DNA polymerase (TAKARA, Japan), and 2 μM of each forward and reverse primer. The PCR program was as follows: 98 °C for 2.5 min, 35 cycles of 98 °C for 10 s, 50 °C for 15 s, and 72 °C for 30 s, and a final extension of 72 °C for 10 min. The PCR products were separated by electrophoresis on 1.2% agarose gel in TAE buffer (40-mM Tris–Acetate, 1-mM EDTA, pH 8.0) and purified from gel with Universal DNA Purification Kit (TIANGEN, China).
Primary assembly of these six fragments was conducted by simultaneous digestion and ligation. The reaction was performed in a 20-µl mixture including 50 ng of each fragment, 1 × T7 ligase buffer, 0.1-mg/ml BSA, 1500-U T7 ligase (NEB, USA), and 5-U BsaI (NEB, USA), with program: 40 cycles of 37 °C for 5 min and 20 °C for 10 min, followed by a final incubation at 20 °C for 60 min. The ligation mixture after a 105- fold dilution was subjected to nested-PCR with primers 5′S-F and 3′S-R, to specifically amplify the assembled PTOX-PTG fragment. 1-μl diluted ligation mix was used as template, and the PCR reaction was performed with the condition described above, except that the annealing temperature was increased to 60 °C.
Finally, the full-length PTOX-PTG fragment was purified from agarose gel, digested by FokI (NEB, USA), and then inserted into the BsaI site of pRGEB32 with T4 ligase (TAKARA, Japan) following the standard manufactory protocols. The generated pRGEB32-PTOX construct was confirmed through Sanger sequencing with primers Crispr_F and Crispr_R.
For genes At1g18170, At1g70270, At1g73655, At1g23965, and At1g74070, the binary vectors carrying desired PTG/Cas9 systems were constructed similarly, while the number and primers of gRNAs were different for different genes.
Empty vector pRGEB32 and pRGEB32 carrying desired PTG/Cas9 were transformed to Agrobacterium tumefaciens strain GV3101, respectively, through the freeze–thaw method. Then, each of them was transformed into Col-0 through Agrobacterium-mediated transformation with the floral dipping method (Clough and Bent 1998). T1 generation seedlings were screened on 1/2 MS medium supplemented with 1% (w/v) sucrose and 20 µg/ml hygromycin. Positive transgenic plants were transferred to soil after 2 weeks.
Mutant screening via PCR analysis
Genomic DNA samples were extracted from Arabidopsis leaves according to the Edward’s Method (Edwards et al. 1991). PCR analysis was applied for examining the targeted gene structure with gene-specific primers. The presence of T-DNA was examined by PCR with the primer pair of Hyg_F/Hyg_R specific for Hygr or Cas9_F/Cas9_R specific for Cas9. The PCR condition was: 30-ng genomic DNA, 1x exTaq Buffer, 1U exTaq (TAKARA, Japan), 2.5 mM of each dNTP, and 0.5 μM of each primer in 15-μl mixture. The PCR reaction followed the program: 94 °C 2.5 min (94 °C 15 s, 58 °C 15 s, and 72 °C 2.5 min) × 35 cycles, 72 °C 10 min. The PCR products were separated on 1% agarose gel in TAE buffer and stained with ethidium bromide. Selected bands were eluted from the gel, and then sequenced directly or cloned into pMD18T vector (TAKARA, Japan) for sequencing. The sequencing chromatograms were viewed with 4Peaks program (v1.7.2).
To quantify the somatic deletion rate of target genes, the stained gels were imaged using a Gel Documentation and Image Analysis System ChampGel 6000 (Beijing Sagecreation, China). Band intensity was quantified in Adobe Photoshop by multiplying the band area with the mean intensity after background subtraction. The somatic deletion rate of each sample was calculated as the intensity percentage of entire shorter bands in all lanes.
Total protein was extracted from rosette leaves and boiled for 10 min in sampling buffer containing 125-mM Tris–HCl (pH 6.8), 4% (w/v) SDS, 2% (v/v) 2-mercaptoethanol, 0.001% (w/v) bromphenol blue, and 20% (v/v) glycerol. The protein samples were separated on a 12% SDS-PAGE gel. Immunoblot analysis against PTOX was done as described previously using a rabbit polyclonal antibody (Fu et al. 2012). Chemiluminescent signals were generated using the ECL Plus reagent (Tanon, China) and visualized using the Tanon-5200 Chemiluminescent Imaging System (Tanon, China).
Six U3 snoRNA promoter sequences were analyzed by multiple sequence alignment software ClustalW (Thompson et al. 1994). Five sequences from A. thaliana (At), Oryza sativa (Os), Triticum aestivum (Ta), and Zea mays (Zm) were obtained from the NCBI website (www.ncbi.nlm.nih.gov), including AtU3b_p (accession No. X52629), AtU3d_p (accession No. X58068), OsU3_p (accession No. X79685), TaU3_p (accession No. X63065), and ZmU3_p (accession No. Z29641). The U3 snoRNA promoter sequence of Gossypium barbadense L. (GbU3_p) was reported by Lei et al. in 2016 (Lei et al. 2016).
Constructing a PTOX-PTG/Cas9 system to edit the PTOX gene in Arabidopsis
In the rice PTG/Cas9 system, expressions of the PTG gene and Cas9 are under the control of a rice U3 snoRNA promoter (OsU3p) and an ubiquitin promoter (OsUBIp), respectively (Xie et al. 2015). We analyzed the conservation of U3 snoRNA promoters (U3p) from several dicotyl and monocotyl land plants using the ClustalW program. It revealed that two key elements, the upstream sequence element (USE, RTCCCACATCG) at position − 60 and the TATA box at position − 25, are highly conserved (Fig. S1), suggesting that OsU3p would function well in Arabidopsis. In addition, the ubiquitin promoter (UBIp) is also conserved in plants (Monia et al. 1990; Ozkaynak et al. 1987). The conservation of U3p and UBIp hinted that the PTG/Cas9 system could be applied directly for gene editing in Arabidopsis. Therefore, we tested whether the original version of the rice PTG/Cas9 system in Arabidopsis works without replacing OsU3p and OsUBIp with their Arabidopsis counterparts, AtU3p and AtUBIp.
In this study, we constructed a PTOX-PTG structure containing five gRNAs evenly targeting the PTOX gene. In detail, gRNA1 and gRNA4 were designed according to the DNA negative strand, and the other three (gRNA2, gRNA3, and gRNA5) were based on the positive strand (Fig. 1a). The PTOX-PTG architecture was amplified in six fragments by PCR with vector pGTR as a template and pre-assembled following the Golden Gate (GG) assembly method described by Xie et al. 2015 (Fig. 1b). Then, the resulting architecture was cloned into the binary vector pRGEB32 at a site downstream of OsU3p, generating vector pRGEB32-PTOX for transforming Arabidopsis (Fig. 1b).
Gene editing of Arabidopsis PTOX in T1 generation
The pRGEB32-PTOX was introduced into Arabidopsis Col-0 through the Agrobacterium-mediated flower-dipping transformation method. We obtained 123 T1 transgenic plants by screening for hygromycin resistance and further PCR confirmation. The majority of transgenic plants looked like wild-type plants, but notably, six plants produced variegated spots in restricted areas (Fig. 2a; Fig. S2a), implying that gene editing of PTOX gene had occurred.
To evaluate the editing efficiency of PTOX–PTG/Cas9 system, we performed a primary analysis on PTOX gene sequence in T1 plant leaf tissue by a simple PCR method with PTOX specific primers (Fig. 1a). Out of these plants, 93 only had a single wild-type sized band (~ 2.5-kb), and 30 (24.4%) produced a few additional shorter bands (Fig. 2b; Fig. S2b). We randomly sequenced three shorter bands from different T1 lines, revealing that they were PTOX variants with different deletions caused by the activity of PTOX-PTG/Cas9 system (Fig. 2b, c). It is noticeable that deletions residing in three examined bands all started from the target site of gRNA1, but ended at the target sites of different gRNAs, i.e., band 1 in gRNA3, band 2 in gRNA4, and band 3 in gRNA5, generating 1069-bp, 1593-bp, and 2093-bp deletions, respectively (Fig. 2c). The distances from the deletion breakpoints to the corresponding PAM sites were within 10 bp except that the 3′-end breakpoint of deletion in band 1 was 50-bp upstream of its corresponding PAM site (Fig. 2c). It suggests that different gRNAs could guide Cas9 to cut their target sites simultaneously, creating two or more DSBs in one DNA molecule and, consequently, resulting in fragmental deletions.
Different PTOX deletion patterns were observed across T1 plants and each ptox variant had a lower intensity compared to the wild-type sized band, indicating that they resulted from somatic gene-editing events and were only presented in a small portion of cells (Fig. 2b; Fig. S2b). We calculated the somatic deletion rate according to the intensity of the short bands, and found that it ranged from 0 to 87.9% (Fig. 2b; Fig. S2b; Table S2). However, the actual somatic editing rate should be higher, because there should be some SNP or small indel mutations, which could not be resolved by gel electrophoresis, as observed in this and previous studies (Xie et al. 2015).
Taken together, the results showed that the rice PTG/Cas9 system was able to edit the PTOX gene in Arabidopsis as we expected, probably due to the conservation of U3p and UBIp promoters in higher plants. In our case, 24.4% of T1 transgenic plants harbored PCR-detectable deletions in the PTOX gene. However, these were all chimeric plants resulting from somatic gene-editing events, and no homozygous ptox mutant was obtained in this generation. Our results agree with previous reports that gene editing by CRISPR/Cas9 mainly occurred at the somatic level in Arabidopsis (Ma et al. 2015; Feng et al. 2014).
Screening homozygous PTOX null mutants in T2 generation
The ultimate goal to apply the PTG/Cas9 system in Arabidopsis is to create homozygous null mutants for further functional research. Although we did not get any homozygous ptox mutant at the T1 generation, 30 T1 plants harboring somatic editing events raised the possibility of achieving the inheritable mutants in their T2 offspring, especially the ones derived from lines with a high ratio of somatic editing events.
We further performed PCR analysis on the PTOX gene of 69 im-like T2 plants from 11 families, including 46 plants from line #46, and 23 plants from 10 other lines (Fig. S3a, b). As a result, 55 plants produced a single ~ 2.5-kb band; seven plants generated a smaller sized single band (Fig. S3a, b). It indicated that these 62 plants were putative homozygotes. In addition, a couple of plants (88-1 and 29-4) produced double bands (Fig. S3a, b), suggesting that they carried two different ptox alleles and were bi-allelic heterozygous mutants. Notably, a small portion of T2 im-like plants (5 plants) still displayed multiple-band patterns, suggesting that somatic editing of the PTOX gene by the PTOX-PTG/Cas9 system could occur in this generation, as well (Fig. S3a, b).
We selected five putative homozygous mutants for further analyses, including three carrying a wild-type sized band (1-1, 29-3, and 78-1), and two with shorter PTOX form (46-21 and 46-22) (Fig. 3a, c). Immunoblot analysis revealed no PTOX protein in these plants, illustrating that they were PTOX null mutants (Fig. 3b). The PCR product amplified by PTOX primers from each putative mutant was sequenced, and results showed that all five plants harbored mutated ptox genes (Fig. 3d), explaining their im-like variegated phenotypes. In these mutants, the sequencing chromatograms of ptox amplicons from plants 1-1, 46-21, 46-24, and 78-1 displayed a high quality and clean signals without any double peak in the whole-gene region, demonstrating that these plants are homozygous mutants. The mutated sites in all four ptox alleles occurred adjacent to the target sites of the designed gRNAs (Fig. 3d). The ptox allele in plant 1-1 (ptox1-1) carried an additional C at the target site of gRNA3. Allele ptox78-1 carried a 1-bp and a 4-bp deletion at the target sites of gRNA3 and gRNA5, respectively. Alleles ptox46-21 and ptox46-24 both harbored a ~ 1-kb deletion between target sites of gRNA3 and gRNA5, and a single-nucleotide insertion at the target site of gRNA2 or gRNA1.
On the contrary, the chromatogram of plant 29-3 had overlapping signals in the region between the target sites of gRNA4 and gRNA5, suggesting that the sample is heterogeneous (Fig. S4a). Therefore, we subcloned the amplicon into the vector pMD-18T, and randomly sequenced ten colonies. The result showed that the PCR product from plant 29-3 consisted of two PTOX isoforms with sequences different around the target sites of gRNA4 and gRNA5 (Fig. 3d, Fig. S4), revealing that plant 29-3 was a bi-allelic mutant exhibiting an im-like phenotype. These two alleles, ptox29-3a and ptox29-3b, both contained a single-nucleotide deletion 4 bp upstream of the gRNA2 PAM site, and ptox29-3b carried two additional indels at the target sites of gRNA4 and gRNA5, which matched the region displaying overlapping sequencing signals (Fig. 3d, Fig. S4).
Altogether, we successfully obtained PTOX homozygous mutants in T2 generation. The five gRNAs seemed to work randomly and unbiasedly in guiding Cas9 to edit the targets. The mutations in T2 homozygous mutants likely originated from somatic gene-editing events occurring in T1 generation. Therefore, T1 plants with a higher somatic editing rate have a higher chance to produce homozygous mutants in their offspring, like in the case of plant #46.
Identifying PTG/Cas9-free homozygous PTOX null mutants
The presence of CRISPR/Cas9 in gene-edited plant will increase the off-target risk, making further complementation test difficult and functional analysis complicated (Gao et al. 2016). It is necessary to remove the PTG/Cas9 system as soon as the mutations are produced. Due to the random integration, the T-DNA carrying PTG/Cas9 is most often not tightly linked with the target gene; therefore, we can easily separate the PTG/Cas9 system from the desired mutant lines simply through natural chromosomal recombination and sequential gene segregation during self-cross.
As to the lines failing to obtain Cas9-free plants in T2 generation, we continued to screen the presence of T-DNA in T3 generation. For instance, we further characterized two putative homozygous mutants carrying obviously shorter ptox alleles (46-4 and 46-5; Fig. 4a) on 1/2 MS medium with hygromycin in T3 generation. Both plants produced 100% of variegated offspring, indicating that they were homozygous. Moreover, plant 46-4 produced ~ 25% hygromycin sensitive and Cas9-free offsprings (Table S3). Since hygromycin only suppresses plant growth but does not kill plants, these sensitive Cas9-free homozygous mutants can be transplanted onto 1/2 MS plate without hygromycin for recovery as they continue to grow in soil.
Gene editing of other Arabidopsis genes with the PTG/Cas9 system
Following the same procedure applied to the PTOX gene, we made a specific PTG/Cas9 construct for each gene and generated corresponding transgenic plants. We started screening T1 transgenic plants for large DNA fragment deletions by PCR. For each gene, we found 15–20 individuals showing multiple bands out of 100 T1 plants. T2 offspring from 2 to 3 T1 plants with somatic deletion rate greater than 20% were analyzed further for the target gene structure and the presence of T-DNA insertion by PCR. We examined about 100 T2 plants in total for each gene. For At1g23965, we found two different Cas9-free homozygous mutant lines. For At1g74070 and At1g70270, we obtained one homozygous and one heterozygous Cas9-free mutant lines. For At1g73655 and At1g18170, we only observed two types of heterozygous mutants. Therefore, we continued the examination on the T3 progeny from these heterozygous T2 mutants to follow the inheritance of the mutation and the presence of T-DNA. Finally, we obtained two different homozygous T-DNA-free mutants for At1g73655 and At1g18170 in T3 generation. All the mutant alleles were sequenced, revealing that the deletions happened between two targets (one of the mutant alleles for each gene is displayed in Fig. 5). Taken together, the rice PTG/Cas9 system was demonstrated to be an efficient gene-editing tool for Arabidopsis.
The PTG/Cas9 system contains a repetitive tRNA-gRNA structure, mimicking the original bacterial CRISPR structure. After being expressed in plant cells, the primary transcript of polycistronic tRNA–gRNA will be processed by endogenous tRNA-processing RNases, producing multiple different gRNAs, which guide Cas9 to edit multiple target sites independently and greatly increase the editing efficiency (Xie et al. 2015). When two or more gRNA-Cas9 complexes cut different sites of a targeted gene simultaneously, it will likely generate DNA fragmental deletions that are suitable for regular PCR examination based on amplicon length polymorphisms of the target genes. Taking advantage of this property, we intentionally developed this PCR-based method to identify desired null mutants created by the PTG/Cas9 system.
Efficiency of the rice PTG/Cas9 system in creating Arabidopsis mutants with large deletion
In this study, we evaluated the rice PTG/Cas9 editing efficiency in creating large deletions in Arabidopsis by a conventional PCR method. In Arabidopsis, we observed that PTOX-PTG/Cas9 resulted in about 25% of T1 transgenic plants generating different extents of PCR-detectable deletions in target regions (Fig. 2b; Fig. S2b; Table S2). In T2 generation, about 20% of the mutants (14 out of 69) carried PCR-detectable deletions (Fig. S3). In rice, only 0–11.76% of T1 transgenic plants showed chromosomal fragment deletion between two targets within a gene (Xie et al. 2015). A comparable ratio was observed in T1 transgenic rice carrying another multiplex editing system (Ma et al. 2015). A probable reason for the high deletion rate in this work is that we designed five gRNAs to target PTOX, whereas the other experiments only applied 2–3 gRNAs for one gene. We reasoned that different gRNAs would guide Cas9 to cut their targets independently, and the deletion between two sites would be generated only when two gRNA-Cas9 complexes land on and cut the same gene at the same time. Increasing the gRNA number for one gene could raise this chance and consequently promote the deletion rate.
The PCR-based examination of large deletions is an easy, quick, and cheap method for screening mutants. However, a downside of this approach is that it would miss all the SNPs or small indels if these mutations do not provoke obvious abnormal phenotypes. According to our observation in T2 generation, most of the mutants (55 out of 69) only carried PCR-undetectable small-scale mutations (Fig. 3; Fig. 4; Fig. S3), just like in the case of rice (Xie et al. 2015). Therefore, this method cannot evaluate the actual overall editing efficiency and editing events. For the purpose, we can conduct the direct Sanger sequencing or PCR–RFLP analysis. Nevertheless, several advanced approaches have proven to be more sensitive, for example, the IDAA method (Yang et al. 2015), the combined qPCR/dPCR analysis of the target genes (Mock et al. 2016; Falabella et al. 2017), and NGS analysis of the target gene amplicons (Sentmanat et al. 2018). In addition, a few algorithms have been developed to robustly verify and quantify the CRISPR/Cas9 edits using Sanger sequencing data, such as ICE (Hsiau et al. 2018) and TIDE (Brinkman et al. 2018). For those who wish to evaluate overall gene-editing events or to identify as many mutants as possible in a limited number of transformants, these methods could be better choices.
High somatic editing rate in T1 plants is crucial for achieving homozygous Arabidopsis mutants
Similar to previous reports (Ma et al. 2015; Feng et al. 2014), most editing events in T1 plants with PTOX-PTG/Cas9 happened in somatic cells. We did not observe homozygous or heterozygous ptox mutant in T1 generation based on PTOX band patterns and their phenotypic segregation patterns in T2 progenies (Fig. 2b; Fig. S2b; Table S2). Therefore, the probability of generating heterozygous or homozygous mutant in T2 generation highly relies on whether T1 somatic editing events occurred in stem cells that would further develop to form gametes. In our work, we used PCR-based examination to roughly estimate and compare the editing efficiency among different transformants carrying the PTG/Cas9 system, because the large deletion rate should be positively correlated with the overall editing efficiency. Our results show that when the somatic deletion ratio is higher than 20%, the plants consistently produce variegated im-like offspring (Table S2). Most of the im-like plants are homozygous plants, and about 20% of them carry alleles with large deletion (Fig. 4; Fig. S3). In contrast, among the T1 lines with a lower somatic deletion ratio (0% < ratio < 20%), only 5 out of 15 lines produced putative homozygous mutants (Table S2). Moreover, out of 93 T1 lines without obvious somatic deletions, only one line produced im-like mutants. Therefore, a high somatic editing rate in T1 plants is crucial for achieving homozygous Arabidopsis mutants successfully and rapidly, i.e., in the first generation or second generation.
A protocol to apply PTG/Cas9 in Arabidopsis
Possible optimizing strategies for applying the PTG/Cas9 system in Arabidopsis
In our work, we directly applied the rice PTG/Cas9 system to edit genes in Arabidopsis without any modification on the major scaffold. It turned out that the rice PTG/Cas9 system could edit genes well in Arabidopsis, probably due to the functional conservation of U3p, tRNA and UBIp between rice and Arabidopsis. However, the processes involved in PTG/Cas9 directed gene editing always have subtle differences amongst plant species, especially the expression and post-transcriptional processing of Cas9 and tRNA–gRNA, which is a prerequisite for the successful application of the PTG/Cas9 system. Rice promoters and tRNAs may not be able to drive the PTG/Cas9 system work with optimal efficiency in Arabidopsis. Therefore, substitution of the rice promoters and tRNAs with those from Arabidopsis would be a good strategy to further optimize this system. Successful application of the PTG/Cas9 system in maize (Qi et al. 2016) and kiwifruit (Wang et al. 2018) are two examples. In these two works, the rice-specific elements in the PTG/Cas9 system, including OsU3p, OstRNA, and OsUBIp, were replaced by corresponding elements from maize and kiwifruit, respectively. The resulting modified systems in both species exhibited a higher editing efficiency compared to the original method in rice.
In addition, increasing the editing efficiency in stem cells would improve the stable transmission of the DNA change, and, therefore, increase the possibility of getting heterozygous or homozygous mutants in fewer generations. It has been shown that the editing efficiency in T1 generation is increased when Cas9 is driven by a promoter of egg cell-specific or meristem-specific genes like EC1.2 (Wang et al. 2015) and Yao (Yan et al. 2015; Li et al. 2018). Heterozygous and homozygous mutants were identified as early as in T1 generation with Cas9 driven by the Yao promoter (Li et al. 2018).
The PTG/Cas9 system was first designed for rice genome editing, and has been used for editing genes in maize and kiwifruit after modification. In this study, we demonstrated that this system also works in Arabidopsis, further indicating that this system has a great potential to edit genes in other plant species. Moreover, by taking advantage of the multiplex PTG/Cas9 system for creating large deletions, we developed a rapid and reliable strategy to identify the aimed Arabidopsis null mutants in three generations with a simple PCR method. Compared to the methods involving mainly screening short indels or SNPs, it reduces DNA sequencing steps, overcomes the limitation of the PCR–RFLP method in selecting suitable gRNA target sites, and minimizes the effort of detecting mutants. This method could also facilitate the mutant screening and identification in other species with any multiplex gene-editing system.
Author contribution statement
MX, AF, YW, and LH designed research; LH, MZ, JH, YH (Yingying Hu), YH (Yanshuang Huo), HH, YH (Yaqi Hao), and WZ performed research; LH, MX, YW, and AF analyzed data; LH, MX, and AF wrote the paper with contributions and approval from all authors.
We thank Dr. Kabin Xie (Huazhong Agriculture University) for providing pGTR and pRGEB32 vectors. We also like to thank Professor Jean-David Rochaix (University of Geneva) for revising the manuscript. This project was supported by National Natural Science Foundation of China (NSFC), No. 31471261 and No. 31270284 to AF and No. 31371226 to MX, Shaanxi Province Education Department Key Laboratory Research Project (No. 13JS108) to MX, and Shaanxi Province Education Department Special Scientific Research Project (No. 16JK1792) to WZ.
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