索引
生物
清脆的
桑格测序
Cas9
遗传学
体细胞无性系变异
基因组
计算生物学
亚基因组mRNA
深度测序
单核苷酸多态性
全基因组测序
基因
DNA测序
基因型
组织培养
体外
作者
Jianying Li,Hakim Manghwar,Lin Sun,Pengcheng Wang,Guanying Wang,Hanyan Sheng,Jie Zhang,Hao Liu,Lei Qin,Hangping Rui,Bo Li,Keith Lindsey,Henry Daniell,Shuangxia Jin,Xianlong Zhang
摘要
Summary The CRISPR /Cas9 system has been extensively applied for crop improvement. However, our understanding of Cas9 specificity is very limited in Cas9‐edited plants. To identify on‐ and off‐target mutation in an edited crop, we described whole genome sequencing ( WGS ) of 14 Cas9‐edited cotton plants targeted to three genes, and three negative (Ne) control and three wild‐type ( WT ) plants. In total, 4188–6404 unique single‐nucleotide polymorphisms ( SNP s) and 312–745 insertions/deletions (indels) were detected in 14 Cas9‐edited plants compared to WT , negative and cotton reference genome sequences. Since the majority of these variations lack a protospacer‐adjacent motif ( PAM ), we demonstrated that the most variations following Cas9‐edited are due either to somaclonal variation or/and pre‐existing/inherent variation from maternal plants, but not off‐target effects. Of a total of 4413 potential off‐target sites (allowing ≤5 mismatches within the 20‐bp sg RNA and 3‐bp PAM sequences), the WGS data revealed that only four are bona fide off‐target indel mutations, validated by Sanger sequencing. Moreover, inherent genetic variation of WT can generate novel off‐target sites and destroy PAM s, which suggested great care should be taken to design sg RNA for the minimizing of off‐target effect. These findings suggested that CRISPR /Cas9 system is highly specific for cotton plants.
科研通智能强力驱动
Strongly Powered by AbleSci AI