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Structural basis for the promiscuous PAM recognition by Corynebacterium diphtheriae Cas9.


ABSTRACT: The RNA-guided DNA endonuclease Cas9 cleaves double-stranded DNA targets bearing a protospacer adjacent motif (PAM) and complementarity to an RNA guide. Unlike other Cas9 orthologs, Corynebacterium diphtheriae Cas9 (CdCas9) recognizes the promiscuous NNRHHHY PAM. However, the CdCas9-mediated PAM recognition mechanism remains unknown. Here, we report the crystal structure of CdCas9 in complex with the guide RNA and its target DNA at 2.9 Å resolution. The structure reveals that CdCas9 recognizes the NNRHHHY PAM via a combination of van der Waals interactions and base-specific hydrogen bonds. Moreover, we find that CdCas9 exhibits robust DNA cleavage activity with the optimal 22-nucleotide length guide RNAs. Our findings highlight the mechanistic diversity of the PAM recognition by Cas9 orthologs, and provide a basis for the further engineering of the CRISPR-Cas9 genome-editor nucleases.

SUBMITTER: Hirano S 

PROVIDER: S-EPMC6488586 | biostudies-literature | 2019 Apr

REPOSITORIES: biostudies-literature

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Structural basis for the promiscuous PAM recognition by Corynebacterium diphtheriae Cas9.

Hirano Seiichi S   Abudayyeh Omar O OO   Gootenberg Jonathan S JS   Horii Takuro T   Ishitani Ryuichiro R   Hatada Izuho I   Zhang Feng F   Nishimasu Hiroshi H   Nureki Osamu O  

Nature communications 20190429 1


The RNA-guided DNA endonuclease Cas9 cleaves double-stranded DNA targets bearing a protospacer adjacent motif (PAM) and complementarity to an RNA guide. Unlike other Cas9 orthologs, Corynebacterium diphtheriae Cas9 (CdCas9) recognizes the promiscuous NNRHHHY PAM. However, the CdCas9-mediated PAM recognition mechanism remains unknown. Here, we report the crystal structure of CdCas9 in complex with the guide RNA and its target DNA at 2.9 Å resolution. The structure reveals that CdCas9 recognizes t  ...[more]

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