C2c2 is a single-component programmable RNA-guided RNA-targeting CRISPR effector

被引:1671
作者
Abudayyeh, Omar O. [1 ,2 ,3 ,4 ,5 ]
Gootenberg, Jonathan S. [2 ,3 ,4 ,5 ,6 ]
Konermann, Silvana [2 ,3 ,4 ,5 ]
Joung, Julia [2 ,3 ,4 ,5 ]
Slaymaker, Ian M. [2 ,3 ,4 ,5 ]
Cox, David B. T. [1 ,2 ,3 ,4 ,5 ,7 ]
Shmakov, Sergey [8 ,9 ]
Makarova, Kira S. [9 ]
Semenova, Ekaterina [10 ]
Minakhin, Leonid [10 ]
Severinov, Konstantin [10 ,11 ]
Regev, Aviv [2 ,7 ]
Lander, Eric S. [2 ,6 ,7 ]
Koonin, Eugene V. [9 ]
Zhang, Feng [1 ,2 ,3 ,4 ,5 ]
机构
[1] MIT, Dept Hlth Sci & Technol, Cambridge, MA 02139 USA
[2] Broad Inst & Harvard, Cambridge, MA 02142 USA
[3] MIT, McGovern Inst Brain Res, Cambridge, MA 02139 USA
[4] MIT, Dept Brain & Cognit Sci, Cambridge, MA 02139 USA
[5] MIT, Dept Biomol Engn, Cambridge, MA 02139 USA
[6] Harvard Med Sch, Dept Syst Biol, Boston, MA 02115 USA
[7] MIT, Dept Biol, 77 Massachusetts Ave, Cambridge, MA 02139 USA
[8] Skolkovo Inst Sci & Technol, Skolkovo 143025, Russia
[9] Natl Lib Med, Natl Ctr Biotechnol Informat, NIH, Bethesda, MD 20894 USA
[10] State Univ New Jersey, Rutgers, Waksman Inst Microbiol, Piscataway, NJ 08854 USA
[11] Russian Acad Sci, Inst Mol Genet, Moscow 123182, Russia
基金
俄罗斯科学基金会;
关键词
ADAPTIVE BACTERIAL IMMUNITY; ESCHERICHIA-COLI; STREPTOCOCCUS-THERMOPHILUS; CRYSTAL-STRUCTURE; CAS IMMUNITY; THERMUS-THERMOPHILUS; SURVEILLANCE COMPLEX; PYROCOCCUS-FURIOSUS; SPACER ACQUISITION; BINDING PROTEINS;
D O I
10.1126/science.aaf5573
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 clustered regularly interspaced short palindromic repeat (CRISPR)-CRISPR-associated genes (Cas) adaptive immune system defends microbes against foreign genetic elements via DNA or RNA-DNA interference. We characterize the class 2 type VI CRISPR-Cas effector C2c2 and demonstrate its RNA-guided ribonuclease function. C2c2 from the bacterium Leptotrichia shahii provides interference against RNA phage. In vitro biochemical analysis shows that C2c2 is guided by a single CRISPR RNA and can be programmed to cleave single-stranded RNA targets carrying complementary protospacers. In bacteria, C2c2 can be programmed to knock down specific mRNAs. Cleavage is mediated by catalytic residues in the two conserved Higher Eukaryotes and Prokaryotes Nucleotide-binding (HEPN) domains, mutations of which generate catalytically inactive RNA-binding proteins. These results broaden our understanding of CRISPR-Cas systems and suggest that C2c2 can be used to develop new RNA-targeting tools.
引用
收藏
页数:9
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