Siddappa Sundaresha, Sharma Neha, Salaria Neha, Thakur Kajal, Pathania Shruti, Singh Baljeet, Sharma Himani, Sood Salej, Bhardwaj Vinay, Thakur Ajay K, Mangal Vikas, Kumar Vinod, Muruthachallam Ravi, Singh Kashmir, Tuli Rakesh
ICAR-Central Potato Research Institute, Shimla, H.P. 171001 India.
Indian Institute of Science Education and Research, Thiruvananthapuram, 695016 India.
3 Biotech. 2023 May;13(5):129. doi: 10.1007/s13205-023-03543-w. Epub 2023 Apr 12.
The gene editing using the CRISPR/Cas9 system has become an important biotechnological tool for studying gene function and improving crops. In this study, we have used CRISPR/Cas9 system for editing the phytoene desaturase gene () in popular Indian potato cultivar Kufri Chipsona-I. A construct (pHSE401) carrying two target gRNAs with glycine tRNA processing system under the control of Arabidopsis U6 promoter and the Cas9 protein was constructed and transformed in potato plants using -mediated genetic transformations. The regeneration efficiency of 45% was observed in regenerated plants, out of which 81% of the putative transformants shoot lines exhibited mutant or bleached phenotype (albinism). The deletion mutations were detected within the gene in the genotyped plants and a mutation efficiency of 72% for gRNA1 and gRNA2 has been detected using Sanger sequencing. Hence, we set up a CRISPR/Cas9-mediated genome editing protocol which is efficient and generates mutations (deletions) within gene in potato. The bleached phenotype is easily detectable after only few weeks after mediated transformation. This is the first report as a proof of concept for CRISPR/Cas9-based editing of gene in Indian potato cv. Kufri Chipsona-I. This study demonstrates that CRISPR/Cas9 can be used to edit genes at high frequency within the genome of the potato for various traits. Therefore, this study will aid in creating important mutants for modifying molecular mechanisms controlling traits of agronomic importance.
利用CRISPR/Cas9系统进行基因编辑已成为研究基因功能和改良作物的重要生物技术工具。在本研究中,我们使用CRISPR/Cas9系统对印度流行马铃薯品种库夫里薯片一号(Kufri Chipsona-I)中的八氢番茄红素去饱和酶基因()进行编辑。构建了一个携带两个靶向gRNA的载体(pHSE401),该载体带有在拟南芥U6启动子控制下的甘氨酸tRNA加工系统和Cas9蛋白,并通过介导的遗传转化将其导入马铃薯植株。在再生植株中观察到45%的再生效率,其中81%的推定转化体芽系表现出突变或白化表型(白化病)。在基因分型植株的基因内检测到缺失突变,使用桑格测序法检测到gRNA1和gRNA2的突变效率为72%。因此,我们建立了一种CRISPR/Cas9介导的基因组编辑方案,该方案高效且能在马铃薯基因内产生突变(缺失)。介导转化后仅几周就能轻松检测到白化表型。这是关于在印度马铃薯品种库夫里薯片一号中基于CRISPR/Cas9对基因进行编辑的概念验证的首次报道。本研究表明,CRISPR/Cas9可用于在马铃薯基因组内高频编辑各种性状的基因。因此,本研究将有助于创建重要突变体,以修饰控制具有农艺重要性性状的分子机制。