Structure and Engineering of Francisella novicida Cas9

被引:273
作者
Hirano, Hisato [1 ]
Gootenberg, Jonathan S. [2 ,3 ,4 ,5 ,6 ]
Horii, Takuro [7 ]
Abudayyeh, Omar O. [2 ,3 ,4 ,5 ]
Kimura, Mika [7 ]
Hsu, Patrick D. [2 ,3 ,4 ,5 ]
Nakane, Takanori [1 ]
Ishitani, Ryuichiro [1 ]
Hatada, Izuho [7 ]
Zhang, Feng [2 ,3 ,4 ,5 ]
Nishimasu, Hiroshi [1 ,8 ]
Nureki, Osamu [1 ]
机构
[1] Univ Tokyo, Grad Sch Sci, Dept Biol Sci, Bunkyo Ku, 2-11-16 Yayoi, Tokyo 1130032, Japan
[2] Broad Inst MIT & Harvard, Cambridge, MA 02142 USA
[3] MIT, McGovern Inst Brain Res, 77 Massachusetts Ave, Cambridge, MA 02139 USA
[4] MIT, Dept Brain & Cognit Sci, E25-618, Cambridge, MA 02139 USA
[5] MIT, Dept Biol Engn, 77 Massachusetts Ave, Cambridge, MA 02139 USA
[6] Harvard Univ, Sch Med, Dept Syst Biol, Boston, MA 02115 USA
[7] Gunma Univ, Inst Mol & Cellular Regulat, Biosignal Genome Resource Ctr, Lab Genome Sci, 3-39-15 Showa Machi, Maebashi, Gunma 3718512, Japan
[8] JST, PRESTO, Bunkyo Ku, 2-11-16 Yayoi, Tokyo 1130032, Japan
关键词
CRYSTAL-STRUCTURE; GUIDE RNA; DUAL-RNA; DNA; CRISPR-CAS9; COMPLEX; SYSTEM; ENDONUCLEASE; CLEAVAGE; IMMUNITY;
D O I
10.1016/j.cell.2016.01.039
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 RNA-guided endonuclease Cas9 cleaves doublestranded DNA targets complementary to the guide RNA and has been applied to programmable genome editing. Cas9-mediated cleavage requires a protospacer adjacent motif (PAM) juxtaposed with the DNA target sequence, thus constricting the range of targetable sites. Here, we report the 1.7 angstrom resolution crystal structures of Cas9 from Francisella novicida (FnCas9), one of the largest Cas9 orthologs, in complex with a guide RNA and its PAM-containing DNA targets. A structural comparison of FnCas9 with other Cas9 orthologs revealed striking conserved and divergent features among distantly related CRISPR-Cas9 systems. We found that FnCas9 recognizes the 5'-NGG-3' PAM, and used the structural information to create a variant that can recognize themore relaxed 5'-YG-3' PAM. Furthermore, wedemonstrated that the FnCas9-ribonucleoprotein complex can be microinjected into mouse zygotes to edit endogenous sites with the 5'-YG-3' PAM, thus expanding the target space of the CRISPR-Cas9 toolbox.
引用
收藏
页码:950 / 961
页数:12
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