| Literature DB >> 26875867 |
Hisato Hirano1, Jonathan S Gootenberg2, Takuro Horii3, Omar O Abudayyeh4, Mika Kimura3, Patrick D Hsu4, Takanori Nakane1, Ryuichiro Ishitani1, Izuho Hatada3, Feng Zhang4, Hiroshi Nishimasu5, Osamu Nureki6.
Abstract
The RNA-guided endonuclease Cas9 cleaves double-stranded 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 Å 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 the more relaxed 5'-YG-3' PAM. Furthermore, we demonstrated 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.Entities:
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Year: 2016 PMID: 26875867 PMCID: PMC4899972 DOI: 10.1016/j.cell.2016.01.039
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582