A Highly Sensitive GFP Activation Assay for Detection of DNA Cleavage in Cells

被引:5
作者
Hu, Ziying [1 ,2 ]
Zhang, Chengdong [1 ]
Wang, Daqi [1 ]
Gao, Siqi [1 ]
Ong, Sang-Ging [3 ,4 ]
Wang, Yongming [1 ,5 ]
Zheng, Wei V. [6 ]
机构
[1] Fudan Univ, Zhongshan Hosp, Sch Life Sci, State Key Lab Genet Engn, Shanghai, Peoples R China
[2] Tongji Univ, Sch Med, Shanghai Matern & Infant Hosp 1, Ctr Assisted Reprod, Shanghai, Peoples R China
[3] Univ Illinois, Dept Pharmacol, Coll Med, Chicago, IL USA
[4] Univ Illinois, Dept Med, Div Cardiol, Coll Med, Chicago, IL USA
[5] Shanghai Engn Res Ctr Ind Microorgan, Shanghai, Peoples R China
[6] Peking Univ, Intervent & Cell Therapy Ctr, Shenzhen Hosp, Shenzhen, Peoples R China
来源
FRONTIERS IN CELL AND DEVELOPMENTAL BIOLOGY | 2021年 / 9卷
基金
中国国家自然科学基金;
关键词
CRISPR; genome editing; DNA cleavage; off-target; PAM; PLURIPOTENT STEM-CELLS; OFF-TARGET CLEAVAGE; CRISPR CAS9; GENOME; SEQ; SPECIFICITY; INTEGRATION; NUCLEASES; VECTOR;
D O I
10.3389/fcell.2021.771248
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
CRISPR/Cas9 nucleases hold great potential for gene therapy, but they frequently induce unwanted off-target cleavage. We previously developed a GFP activation assay for detection of DNA cleavage in cells. Here, we demonstrate two novel applications of this assay. First, we use this assay to confirm off-target cleavage that cannot be detected by targeted deep sequencing in cells before. Second, we use this approach to detect multiple alternative PAMs recognized by SpCas9. These noncanonical PAMs are associated with low cleavage activity, but targets associated with these PAMs must be considered as potential off-target sites. Taken together, the GFP activation assay is a powerful platform for DNA cleavage detection in cells.
引用
收藏
页数:9
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