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dc.contributor.authorYamada, Mari
dc.contributor.authorWatanabe, Yuto
dc.contributor.authorHirano, Hisato
dc.contributor.authorRan, F. Ann
dc.contributor.authorNakane, Takanori
dc.contributor.authorIshitani, Ryuichiro
dc.contributor.authorNishimasu, Hiroshi
dc.contributor.authorNureki, Osamu
dc.contributor.authorGootenberg, Jonathan S
dc.contributor.authorZhang, Feng
dc.date.accessioned2018-04-25T17:38:12Z
dc.date.available2018-04-25T17:38:12Z
dc.date.issued2017-03
dc.date.submitted2017-01
dc.identifier.issn1097-2765
dc.identifier.issn1097-4164
dc.identifier.urihttp://hdl.handle.net/1721.1/114953
dc.description.abstractThe RNA-guided endonuclease Cas9 generates a double-strand break at DNA target sites complementary to the guide RNA and has been harnessed for the development of a variety of new technologies, such as genome editing. Here, we report the crystal structures of Campylobacter jejuni Cas9 (CjCas9), one of the smallest Cas9 orthologs, in complex with an sgRNA and its target DNA. The structures provided insights into a minimal Cas9 scaffold and revealed the remarkable mechanistic diversity of the CRISPR-Cas9 systems. The CjCas9 guide RNA contains a triple-helix structure, which is distinct from known RNA triple helices, thereby expanding the natural repertoire of RNA triple helices. Furthermore, unlike the other Cas9 orthologs, CjCas9 contacts the nucleotide sequences in both the target and non-target DNA strands and recognizes the 5′-NNNVRYM-3′ as the protospacer-adjacent motif. Collectively, these findings improve our mechanistic understanding of the CRISPR-Cas9 systems and may facilitate Cas9 engineering. Keywords: CRISPR-Cas system; Cas9; protospacer adjacent motif; RNA triplex; crystal structureen_US
dc.description.sponsorshipUnited States. Department of Energy (Grant DE-FG02-97ER25308)en_US
dc.description.sponsorshipNational Institute of Mental Health (U.S.) (Grant 5DP1-MH100706)en_US
dc.description.sponsorshipNational Institute of Mental Health (U.S.) (Grant 1R01-MH110049)en_US
dc.language.isoen_US
dc.publisherElsevieren_US
dc.relation.isversionofhttps://doi.org/10.1016/j.molcel.2017.02.007en_US
dc.rightsCreative Commons Attribution-NonCommercial-NoDerivs Licenseen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/en_US
dc.sourceProf. Zhang via Courtney Crummetten_US
dc.titleCrystal Structure of the Minimal Cas9 from Campylobacter jejuni Reveals the Molecular Diversity in the CRISPR-Cas9 Systemsen_US
dc.typeArticleen_US
dc.identifier.citationYamada, Mari et al. “Crystal Structure of the Minimal Cas9 from Campylobacter Jejuni Reveals the Molecular Diversity in the CRISPR-Cas9 Systems.” Molecular Cell 65, 6 (March 2017): 1109–1121 © 2017 Elsevier Incen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biological Engineeringen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Brain and Cognitive Sciencesen_US
dc.contributor.departmentMcGovern Institute for Brain Research at MITen_US
dc.contributor.approverZhang, Fengen_US
dc.contributor.mitauthorGootenberg, Jonathan S
dc.contributor.mitauthorZhang, Feng
dc.relation.journalMolecular Cellen_US
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsYamada, Mari; Watanabe, Yuto; Gootenberg, Jonathan S.; Hirano, Hisato; Ran, F. Ann; Nakane, Takanori; Ishitani, Ryuichiro; Zhang, Feng; Nishimasu, Hiroshi; Nureki, Osamuen_US
dspace.embargo.termsNen_US
dc.identifier.orcidhttps://orcid.org/0000-0003-2782-2509
mit.licensePUBLISHER_CCen_US


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