TALEN is an artificial nuclease being applied for sequence-specific genome editing. For the plant genome editing, a pair of TALEN genes is expressed in the cells, and a binary plasmid for Agrobacterium-mediated transformation should be assembled. We developed a novel procedure using the Gateway-assisted plasmids, named Emerald–Gateway TALEN system. We constructed entry vectors, pPlat plasmids, for construction of a desired TALEN gene using Platinum Gate TALEN kit. We also created destination plasmid, pDual35SGw1301, which allowed two TALEN genes to both DNA strands to recruit using Gateway technology. Resultant TALEN genes were evaluated by the single-strand annealing (SSA) assay in E. coli cells. By this assay, the TALENs recognized the corresponding targets in the divided luciferase gene, and induced a specific recombination to generate an active luciferase gene. Using the TALEN genes constructed, we created a transformant potato cells in which a site-specific mutation occurred at the target site of the GBSS gene. This suggested that our system worked effectively and was applicable as a convenient tool for the plant genome editing.
Targeted genome modifications will become routine in near future in crop plants1. A number of new genome editing technologies have been developed, including zinc finger nucleases (ZFNs), transcription activator like effector nucleases (TALENs), and clustered regulatory interspaced palindromic repeats/Cas9 (CRISPR/Cas9) systems2. These sequence-specific nucleases create double strand breaks (DSBs) at the targeted loci3. They induce subsequent repairs of the genomes in living cells, such as non-homologous end joining (NHEJ) and homologous recombination (HR). These events cause site-directed mutagenesis and/or integrations of desired DNA fragments at the targeted sites4.
TALEN is a sequence-specific nuclease created by fusing transcription activator like effectors (TALEs) to the catalytic domain of the FokI endonuclease5. TALEN shows high genome editing activity with low toxicity in human cells6, and leads to efficient plant genome engineering7. The DNA binding domains of TALENs contain highly homologous 34 amino acid direct repeats (34-aa repeats) determining specificity8. In the DNA binding domain, there are specific binding motifs, two hypervariable amino-acid residues known as repeat-variable di-residues (RVDs), each of which recognizes one base pair in the target DNA9. Among the RVDs, NI, HD, NH/NK and NG strictly recognize adenine, cytosine, guanine, and thymine nucleotides, respectively, whereas some RVDs, such as NN and NS, show degenerated specificity to guanine and adenine nucleotides8. If high specificity for guanine is required, the RVDs NH or NK are preferred, but RVD NN should be chosen if weak overall efficiency of the TALE needs to be increased10. To construct the DNA binding motifs of TALEN for the desired target sequence, the efficient systems, such as Platinum Gate system, have been developed11. Gateway-assisted assemble systems have been applied for the animal genome editing. Using this system, a single plasmid containing two TALEN genes that were driven by the CAG promoter and human EF1α promoter, respectively, were developed for editing of the vertebrate genome12.
In case of plant genome editing, a pair of TALEN genes needs to be introduced and expressed in the cells. However, it requires bothersome works to assemble them in a binary vector for the Agrobacterium-mediated transformation of the plant cells. Here, we propose a Gateway-assisted construction of TALEN genes, which leads to rapid creation of a desired binary plasmid.
Development of Emerald-Gateway TALEN system
We employed the Platinum Gate TALEN kit11 to adapt for the Gateway technology that enabled rapidly assembling the desired TALEN genes in a binary vector. We produced a series of the pPlat vectors, which functioned as Gateway entry vectors containing a cloning site between two Esp3I sites at the region corresponding to the DNA-binding domain in the platinum TALEN (Fig. 1A). For the destination vector, we created a plasmid, pDual35SGw1301, which contained two cloning cassettes composed by the cauliflower mosaic virus (CaMV) 35S promoter followed by the recombination sites for the Gateway technology (Fig. 1B). Pieces in the DNA-binding domain corresponding to the desired target nucleotide sequence were inserted into an appropriate pPlat vector according to the procedure of the Platinum Gate TALEN kit. A pair of the resultant TALEN genes was simultaneously transferred into the destination vectors by the Gateway system. In this system, it is expected that these genes in the resultant plasmid are expressed under 35S promoters (Fig. 2). We named our system using pPlat plasmids and the destination vector as “Emerald-Gateway TALEN system”.
Construction of the TALEN genes
There are eight kinds of pPlat plasmids that contain different C-terminal RVDs at the 34-aa repeat in the divided TALEN gene and each of two resistant markers (Fig. 1A). We designed two sets of target sequences of TALENs, which were located in the potato granule-bound starch synthase (GBSS) gene. We obtained the desired TALENs in a pPlat plasmid using the Platinum Gate system (see Methods). The resultant plasmids for a pair of the TALEN genes were subjected to the Gateway-mediated assembly in pDual35SGw1301. Our system generated four types of destination plasmids, which showed differences in direction of the TALEN genes and attached resistant genes (Fig. 3). The desired plasmid including a heterologous pair of TALEN genes was selected by resistance to Kanamycin, Chloramphenicol, and Ampicillin, and by formation of blue colonies on the X-Gal plates.
Evaluation of the constructed TALENs
We performed single-strand annealing (SSA) assay, which was widely used for determination of double-strand DNA breakage13, coupled with a luciferase (Luc) assay. We evaluated the function of the constructed TALENs by SSA assays using the target sequences in GBSS gene, which were localized in the different points of the gene (see Supplemental Fig. 1). The target sequences were put into the divided Luc gene, and they were introduced into E. coli cells together with the TALEN genes. After the target sequence was digested by the appropriate TALENs, it was expected that the mature Luc gene was reconstructed from the divided Luc gene by the simultaneous recombination, and that the Luc activity arose in the cells.
The significantly high level of Luc activity was detected in E. coli cells harboring the divided Luc gene together with the appropriate TALEN genes (Fig. 4B, combination of TALEN “ab” and a reporter plasmid “ab”, and that of TALEN “cd” and a reporter “cd”), whereas a basal level of Luc activity was shown in the transformant cells containing the divided Luc gene with the sequence that was not the target of the introduced TALENs (Fig. 4B, combination of TALEN “cd” and a reporter “ab”, and that of TALEN “ab” and a reporter “cd”). These results indicate that the TALENs specifically recognized the target sequence, and induced an SSA event. This suggested that these TALENs were efficiently functioned.
Using the TALEN genes constructed, we transformed potato cells to induce a mutation at the target site of the GBSS gene. From the transgenic callus cells, we extracted the genomic DNA, and amplified the fragment corresponding to the GBSS gene in which the target sequence was included. We detected the fragments lacking the HindIII digestion site at the target site of the TALENs. We found three kinds of genome modifications that had occurred independently. We detected 63 nucleotides deletion, one nucleotide insertion, and one nucleotide substitution at the HindIII site (Fig. 4C). This suggests that the site-specific mutation occurred at the target site in the potato cells in planta.
We developed a novel TALEN construction system, named Emerald Gateway TALEN system, which was customized for Gateway system using Platinum Gate TALEN kit. Our system composed of two-step procedures to produce a pair of TALEN genes for the plant genome editing. In the first step, a pair of entry plasmids containing each of the desired TALEN genes was constructed using pPlat plasmids. The resultant TALEN genes were then introduced into a binary vector as a destination plasmid by the second step to generate a desired binary plasmid (Fig. 2).
A TALEN gene includes highly repetitive sequences, and therefore it is difficult to construct a plasmid consisting of the desired structure. Our system needs a destination vector that contains two sets of expression units composed of appropriate promoters and following acceptor sequences of Gateway attR1/2, to which each of desired TALEN genes is inserted. pPlat plasmids are entry vectors that are available for construction of a binary plasmid by Gateway technology (Fig. 2). Once the TALEN genes were constructed using pPlat plasmids, they can be efficiently transferred into a destination vector.
In this study, we prepared the desired binary plasmids in a week, suggesting that our system allows high efficiency and reliability for construction of the binary plasmid that contains the desired TALEN genes without requirement of much purification processes on the intermediate products. A desired pair of TALEN genes was easily obtained by a quadruple selection by resistance to three antibiotics, and by blue-white selection using X-Gal, to obtain. We propose a general protocol for construction of the TALENs by our system (see Supplemental materials). This procedure results in reduction of labors compared with those required in the conventional TALEN gene construction processes, and leads to timesaving experiment on the plant genome editing.
SSA assay using E. coli cells detected the Luc activity that was induced by the mutagenesis at the specific target sequence (Fig. 4). It was known that the 35S promoter worked in E. coli cells14. This result suggests that the resultant TALEN genes effectively functioned for the genome editing events in the cells. In addition, we obtained the transformant potato cells using the constructed TALEN genes (Fig. 4C). These facts show that our system is reliable for the tools to construct the active TALEN genes for the plant genome editing.
In this work, we employed CaMV 35S promoter for expression of TALEN genes in the destination vector. These CaMV 35S promoter regions were located between XbaI and KpnI sites in the destination plasmid (Fig. 2E), and easily replaced by any other promoters. This suggests that an appropriate destination vector can be constructed conveniently depending on the demands.
We used E. coli strain NEB stable (New England Biolab, MA, USA) that is expected to reduce unexpected recombination in repeat sequences for the plasmid construction. Platinum Gate TALEN kit was obtained from Addgene (#1000000043, Cambridge, MA, USA).
Construction of vector plasmids
Entry plasmids, named as a series of pPlatA and pPlatC, were constructed using pDONR207 (Invitrogen, Carlsbad, USA). Depending to the resistant genes for the selection marker, we generated two different types of plasmids. Desired TALEN genes were employed in the entry plasmids using Platinum Gate TALEN kit11. A destination plasmid, pDual35SGw1301, was constructed using pGWB215 and pCAMBIA1301 (CAMBIA, Australia). Detailed methods of the plasmid construction were described in Supplemental Methods.
Construction of TALEN genes
In this work, following sequences contained in the potato GBSS gene (acc. no. NW_006238976) was used as the targets of TALENs: 5′-TGGTTTAAGGGCTGTTaacaagcttgatgggCTCCAATCAAGAACTAA, and 5′-TGTGATCCGCTACTTTAtctgcaggtcaaagtTGGAGACAGCATTGAAA (capital letters indicate the sequence recognized by the corresponding TALENs), respectively. The regions of the 34-aa repeats containing appropriate RVDs for the recognition sites of the TALENs were constructed using the Platinum Gate TALEN kit11 with following modifications. We used pPlat plasmids as the acceptor plasmids. The resultant TALEN genes were assembled into pDual35SGw1301 by Gateway LR clonaseII (Invitrogen). The resultant plasmids were prepared using a Fastgene miniprep kit (Nippon Genetics, Tokyo, Japan) from the E. coli cells that were selected as blue colonies on the plate containing X-Gal with resistance to Kanamycin, Ampicillin and Chloramphenicol.
Construction of plasmids for SSA assays
The SSA vector plasmid, pSSARL-GwBP, was constructed using pBluescriptII SK+ by introduction of CaMV 35S promoter followed by the coding sequences for the Renilla luciferase, self-cleavable 2A peptide16, the divided Luc, and Nos terminator. The regions for 35S promoter and RLuc were amplified by PCR from pCAMBIA1301 and pRL-null (Picagene Dual Seapansy Luminescence kit, Toyo-B-net, Tokyo, Japan), respectively. The fragment of 2A and the divided Luc gene was chemically synthesized. This gene contained the coding region for the first from two-thirds of the Luc gene (from 1 to 1035 nucleotide position) and the region behind the third of the Luc gene (from 605 and later), in which the 430 nucleotides was repeated in the border region. Inside the divided Luc, there was a gateway attP site to which the desired sequence was introduced by BP clonase to generate pSSARL-GwBP. The target fragment (50 nucleotides) of the TALENs for the potato GBSS gene was chemically synthesized, and introduced into pSSARL-GwBP by the reaction of BP clonase, to generate each of the SSA target plasmids, pSSARLab and pSSARLcd. Detailed methods of the plasmid construction were described in Supplemental Methods.
E. coli cells were transformed by introduction of the plasmids each of which contained for the SSA target sequence and the TALEN genes. The transformant cells showing resistance both to Kanamycin and Ampicillin were grown for 16 hours in a medium containing 1% peptone, 0.5% yeast extract, and 0.5% NaCl at 37 °C. The Luc activity was determined by the fluorometric assay method using Picagene Dual Seapangy Luminescence kit (Toyo-B-net, Japan) and Luminometer ARVO light (PerkinElmer, MA). Renilla luciferase activity was measured as the internal control. Luc activities derived from the introduced SSA target plasmid were normalized as the relative values to the Renilla luciferase activity.
Detection of site-specific mutation in the target gene
A fragment corresponding to the region including the target site of the TALEN genes was amplified by PCR using a high-fidelity KOD FX neo DNA polymerase (Toyobo) from the genomic DNA of the transformant potato callus, which was created by the Agrobacterium-mediated transformation method using the appropriate TALEN genes. The amplified fragment was cleaved by HindIII to enrich the population of fragments lacking the HindIII site. The resultant fragments were introduced into pBluescriptII SK + (Toyobo), and cloned in E. coli cells. From the generated E. coli cells, the fragment containing the target site was amplified by PCR. Site-specific mutation at the target site of the TALENs was determined by generation of the fragment that was not digested by HindIII. Detailed methods of the plasmid construction were described in Supplemental Methods.
Accession Codes: Accession numbers of the nucleotide sequences of the plasmids produced in this work are LC122497 (pPlatA63HD), LC122498 (pPlatA63NG), LC122499 (pPlatA63NI), LC122500 (pPlatA63NN), LC122501 (pPlatC63HD), LC122502 (pPlatC63NG), LC122503 (pPlatC63NI), LC122504 (pPlatC63NN), LC122496 (pDual35SGw1301), and LC122270 (pSSARL-GwBP), respectively.
How to cite this article: Kusano, H. et al. A simple Gateway-assisted construction system of TALEN genes for plant genome editing. Sci. Rep. 6, 30234; doi: 10.1038/srep30234 (2016).
We thank to Dr. T. Sakuma, T. Yamamoto, N. Kawano and K. Yoshimatsu for technical advices. This work was supported in part by a grant of Cross-ministerial Strategic Innovation Promotion Program (SIP), and by a Health, Labour and Welfare Grant-in-Aid for Scientific Research.
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Plant Physiology and Biochemistry (2018)