CRISPR-assisted detection of RNA-protein interactions in living cells

被引:89
|
作者
Yi, Wenkai [1 ,2 ]
Li, Jingyu [2 ,3 ]
Zhu, Xiaoxuan [2 ,3 ]
Wang, Xi [1 ,4 ]
Fan, Ligang [1 ,2 ]
Sun, Wenju [1 ]
Liao, Linbu [1 ]
Zhang, Jilin [5 ]
Li, Xiaoyu [1 ,2 ]
Ye, Jing [6 ]
Chen, Fulin [1 ]
Taipale, Jussi [5 ,7 ]
Chan, Kui Ming [2 ,3 ]
Zhang, Liang [2 ,3 ]
Yan, Jian [1 ,2 ]
机构
[1] Northwest Univ, Sch Med, Xian, Peoples R China
[2] City Univ Hong Kong, Dept Biomed Sci, Hong Kong, Peoples R China
[3] City Univ Hong Kong, Shenzhen Res Inst, Biotech & Hlth Ctr, Key Lab Biochip Technol, Shenzhen, Peoples R China
[4] German Canc Res Ctr, Div Theoret Syst Biol, Heidelberg, Germany
[5] Karolinska Inst, Dept Med Biochem & Biophys, Stockholm, Sweden
[6] Fourth Mil Med Univ, Dept Pathol, Xian, Peoples R China
[7] Univ Cambridge, Dept Biochem, Cambridge, England
基金
中国国家自然科学基金;
关键词
NONCODING RNA; GENES; HISAT;
D O I
10.1038/s41592-020-0866-0
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
CARPID uses CRISPR technology to navigate biotin ligase to specific lncRNAs, which allows proximal labeling and thus the querying of RNA-protein interactions in living cells. We have developed CRISPR-assisted RNA-protein interaction detection method (CARPID), which leverages CRISPR-CasRx-based RNA targeting and proximity labeling to identify binding proteins of specific long non-coding RNAs (lncRNAs) in the native cellular context. We applied CARPID to the nuclear lncRNA XIST, and it captured a list of known interacting proteins and multiple previously uncharacterized binding proteins. We generalized CARPID to explore binders of the lncRNAs DANCR and MALAT1, revealing the method's wide applicability in identifying RNA-binding proteins.
引用
收藏
页码:685 / +
页数:17
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