Wang Xianhang, Tu Mingxing, Wang Ya, Yin Wuchen, Zhang Yu, Wu Hongsong, Gu Yincong, Li Zhi, Xi Zhumei, Wang Xiping
State Key Laboratory of Crop Stress Biology in Arid Areas, College of Horticulture, Northwest A&F University, 712100, Yangling, Shaanxi, China.
College of Enology, Northwest A&F University, 712100, Yangling, Shaanxi, China.
Hortic Res. 2021 May 1;8(1):114. doi: 10.1038/s41438-021-00549-4.
The CRISPR (clustered regularly interspaced short palindromic repeats)-associated protein 9 (Cas9) system is a powerful tool for targeted genome editing, with applications that include plant biotechnology and functional genomics research. However, the specificity of Cas9 targeting is poorly investigated in many plant species, including fruit trees. To assess the off-target mutation rate in grapevine (Vitis vinifera), we performed whole-genome sequencing (WGS) of seven Cas9-edited grapevine plants in which one of two genes was targeted by CRISPR/Cas9 and three wild-type (WT) plants. In total, we identified between 202,008 and 272,397 single nucleotide polymorphisms (SNPs) and between 26,391 and 55,414 insertions/deletions (indels) in the seven Cas9-edited grapevine plants compared with the three WT plants. Subsequently, 3272 potential off-target sites were selected for further analysis. Only one off-target indel mutation was identified from the WGS data and validated by Sanger sequencing. In addition, we found 243 newly generated off-target sites caused by genetic variants between the Thompson Seedless cultivar and the grape reference genome (PN40024) but no true off-target mutations. In conclusion, we observed high specificity of CRISPR/Cas9 for genome editing of grapevine.
成簇规律间隔短回文重复序列(CRISPR)相关蛋白9(Cas9)系统是一种用于靶向基因组编辑的强大工具,其应用包括植物生物技术和功能基因组学研究。然而,包括果树在内的许多植物物种中,Cas9靶向的特异性研究较少。为了评估葡萄(Vitis vinifera)中的脱靶突变率,我们对7株经Cas9编辑的葡萄植株和3株野生型(WT)植株进行了全基因组测序(WGS),其中7株经Cas9编辑的葡萄植株中有一株的两个基因之一被CRISPR/Cas9靶向。与3株野生型植株相比,我们在7株经Cas9编辑的葡萄植株中总共鉴定出202,008至272,397个单核苷酸多态性(SNP)以及26,391至55,414个插入/缺失(indel)。随后,选择了3272个潜在脱靶位点进行进一步分析。从WGS数据中仅鉴定出1个脱靶indel突变,并通过桑格测序进行了验证。此外,我们发现由汤普森无核品种与葡萄参考基因组(PN40024)之间的遗传变异导致的243个新产生的脱靶位点,但没有真正的脱靶突变。总之,我们观察到CRISPR/Cas9对葡萄基因组编辑具有高度特异性。