Structural roles of guide RNAs in the nuclease activity of Cas9 endonuclease

被引:88
|
作者
Lim, Youngbin [1 ]
Bak, So Young [2 ]
Sung, Keewon [2 ]
Jeong, Euihwan [2 ]
Lee, Seung Hwan [3 ]
Kim, Jin-Soo [2 ,3 ]
Bae, Sangsu [2 ,3 ,4 ]
Kim, Seong Keun [1 ,2 ]
机构
[1] Seoul Natl Univ, Dept Biophys & Chem Biol, Seoul 151747, South Korea
[2] Seoul Natl Univ, Dept Chem, Seoul 151747, South Korea
[3] Inst for Basic Sci Korea, Ctr Genome Engn, Seoul 151747, South Korea
[4] Hanyang Univ, Dept Chem, Seoul 133791, South Korea
来源
NATURE COMMUNICATIONS | 2016年 / 7卷
基金
新加坡国家研究基金会;
关键词
TARGET DNA RECOGNITION; SINGLE-MOLECULE FRET; COMPLEX; CRISPR-CAS9; SPECIFICITY; PROKARYOTES; RESISTANCE; CLEAVAGE; IMMUNITY; REPEATS;
D O I
10.1038/ncomms13350
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The type II CRISPR-associated protein Cas9 recognizes and cleaves target DNA with the help of two guide RNAs (gRNAs; tracrRNA and crRNA). However, the detailed mechanisms and kinetics of these gRNAs in the Cas9 nuclease activity are unclear. Here, we investigate the structural roles of gRNAs in the CRISPR-Cas9 system by single-molecule spectroscopy and reveal a new conformation of inactive Cas9 that is thermodynamically more preferable than active apo-Cas9. We find that tracrRNA prevents Cas9 from changing into the inactive form and leads to the Cas9: gRNA complex. For the Cas9: gRNA complex, we identify sub-conformations of the RNA-DNA heteroduplex during R-loop expansion. Our single-molecule study indicates that the kinetics of the sub-conformations is controlled by the complementarity between crRNA and target DNA. We conclude that both tracrRNA and crRNA regulate the conformations and kinetics of the Cas9 complex, which are crucial in the DNA cleavage activity of the CRISPR-Cas9 system.
引用
收藏
页数:8
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