CRISPR/Cas9介导下高效敲除SQSTM1/p62基因的Hela细胞模型的建立

目的 :探讨针对p62双sgRNA向导CRISPR/Cas9基因编辑效率。方法 :采用CRISPR/Cas9基因编辑技术成功敲除p62基因,通过细胞有限稀释法和嘌呤霉素筛选,免疫印迹法验证双sgRNA和单sgRNA向导的基因编辑成功率;流式细胞仪验证p62缺失对Hela细胞凋亡的影响。结果 :免疫印迹分析得出双sgRNA导向的p62敲除效率高于单sgRNA导向的敲除,靶序列测序比对分析确认p62编码基因发生大片段缺失突变。H_2O_2处理稳定敲除的Hela细胞系显示,p62基因敲除能明显抑制Hela细胞H_2O_2诱导的早期细胞凋亡。结论 :成功建立了p62敲除的Hela细胞系,双sgRNA向导的CRISPR/Cas9基因编辑体系可能是一种更有效的编辑工具。

Establishment of SQSTM1/p62 gene knockout Hela cells by CRISPR/Cas9

Objective:To explore the editing efficiency of the dual sgRNA guided CRISPR/Cas9 gene targeting p62 protein.Methods:Hela cells with p62 knockout were screened with limited dilution and puromycin treatment after CRISPR/Cas9 gene editing,the success rate of gene editing guided by dual sgRNA and single sgRNA was verified using Western blotting,and the rate of apoptosis was analyzed by flow cytometry.Results:Western blotting analysis indicated that the effect of knockout via dual sgRNA-targeted p62 was elevated than that of single sgRNA,and targetsequence comparison revealed that the large fragment was deleted in p62 knockout cells.After H2O2 treatment,the p62 knockout cells inhibited early apoptosis in Hela cells.Conclusion:The p62 knockout Hela cell line is successfully established,and the CRISPR/Cas9 gene editing system guided by dual sgRNA may be a more effective editing tool.