Cpf1 Is a Single RNA-Guided Endonuclease of a Class 2 CRISPR-Cas System

被引:3570
作者
Zetsche, Bernd [1 ,2 ,3 ,4 ,5 ]
Gootenberg, Jonathan S. [1 ,2 ,3 ,4 ,6 ]
Abudayyeh, Omar O. [1 ,2 ,3 ,4 ]
Slaymaker, Ian M. [1 ,2 ,3 ,4 ]
Makarova, Kira S. [7 ]
Essletzbichler, Patrick [1 ,2 ,3 ,4 ]
Volz, Sara E. [1 ,2 ,3 ,4 ]
Joung, Julia [1 ,2 ,3 ,4 ]
van der Oost, John [8 ]
Regev, Aviv [1 ,9 ]
Koonin, Eugene V. [7 ]
Zhang, Feng [1 ,2 ,3 ,4 ]
机构
[1] Broad Inst MIT & Harvard, Cambridge, MA 02142 USA
[2] MIT, McGovern Inst Brain Res, Cambridge, MA 02139 USA
[3] MIT, Dept Brain & Cognit Sci, Cambridge, MA 02139 USA
[4] MIT, Dept Biol Engn, Cambridge, MA 02139 USA
[5] Bonn Med Sch, Inst Pathol, Dept Dev Pathol, D-53127 Bonn, Germany
[6] Harvard Univ, Sch Med, Dept Syst Biol, Boston, MA 02115 USA
[7] NIH, Natl Ctr Biotechnol Informat, Natl Lib Med, Bethesda, MD 20894 USA
[8] Wageningen Univ, Dept Agrotechnol & Food Sci, Microbiol Lab, NL-6703 HB Wageningen, Netherlands
[9] MIT, Howard Hughes Med Inst, Dept Biol, Cambridge, MA 02139 USA
关键词
CRYSTAL-STRUCTURE; STREPTOCOCCUS-THERMOPHILUS; SURVEILLANCE COMPLEX; ADAPTIVE IMMUNITY; ESCHERICHIA-COLI; TARGET DNA; BACTERIA; SPECIFICITY; PROKARYOTES; CLEAVAGE;
D O I
10.1016/j.cell.2015.09.038
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The microbial adaptive immune system CRISPR mediates defense against foreign genetic elements through two classes of RNA-guided nuclease effectors. Class 1 effectors utilize multi-protein complexes, whereas class 2 effectors rely on single-component effector proteins such as the well-characterized Cas9. Here, we report characterization of Cpf1, a putative class 2 CRISPR effector. We demonstrate that Cpf1 mediates robust DNA interference with features distinct from Cas9. Cpf1 is a single RNA-guided endonuclease lacking tracrRNA, and it utilizes a T-rich protospacer-adjacent motif. Moreover, Cpf1 cleaves DNA via a staggered DNA double-stranded break. Out of 16 Cpf1-family proteins, we identified two candidate enzymes from Acid-aminococcus and Lachnospiraceae, with efficient genome-editing activity in human cells. Identifying this mechanism of interference broadens our understanding of CRISPR-Cas systems and advances their genome editing applications.
引用
收藏
页码:759 / 771
页数:13
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