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dc.contributor.authorShmakov, Sergey
dc.contributor.authorMakarova, Kira S.
dc.contributor.authorWolf, Yuri I.
dc.contributor.authorSemenova, Ekaterina
dc.contributor.authorMinakhin, Leonid
dc.contributor.authorSeverinov, Konstantin
dc.contributor.authorKoonin, Eugene V.
dc.contributor.authorAbudayyeh, Omar Osama
dc.contributor.authorGootenberg, Jonathan S
dc.contributor.authorJoung, Julia
dc.contributor.authorKonermann, Silvana M
dc.contributor.authorZhang, Feng
dc.date.accessioned2017-12-13T14:25:36Z
dc.date.available2017-12-13T14:25:36Z
dc.date.issued2015-10
dc.date.submitted2015-09
dc.identifier.issn1097-2765
dc.identifier.issn1097-4164
dc.identifier.urihttp://hdl.handle.net/1721.1/112723
dc.description.abstractMicrobial CRISPR-Cas systems are divided into Class 1, with multisubunit effector complexes, and Class 2, with single protein effectors. Currently, only two Class 2 effectors, Cas9 and Cpf1, are known. We describe here three distinct Class 2 CRISPR-Cas systems. The effectors of two of the identified systems, C2c1 and C2c3, contain RuvC-like endonuclease domains distantly related to Cpf1. The third system, C2c2, contains an effector with two predicted HEPN RNase domains. Whereas production of mature CRISPR RNA (crRNA) by C2c1 depends on tracrRNA, C2c2 crRNA maturation is tracrRNA independent. We found that C2c1 systems can mediate DNA interference in a 5'-PAM-dependent fashion analogous to Cpf1. However, unlike Cpf1, which is a single-RNA-guided nuclease, C2c1 depends on both crRNA and tracrRNA for DNA cleavage. Finally, comparative analysis indicates that Class 2 CRISPR-Cas systems evolved on multiple occasions through recombination of Class 1 adaptation modules with effector proteins acquired from distinct mobile elements.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.description.sponsorshipNational Institute of Diabetes and Digestive and Kidney Diseases (U.S.) (Grant 5R01DK097768-03)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant GM10407)en_US
dc.publisherElsevieren_US
dc.relation.isversionofhttp://dx.doi.org/10.1016/J.MOLCEL.2015.10.008en_US
dc.rightsCreative Commons Attribution-NonCommercial-NoDerivs Licenseen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/en_US
dc.sourcePMCen_US
dc.titleDiscovery and Functional Characterization of Diverse Class 2 CRISPR-Cas Systemsen_US
dc.typeArticleen_US
dc.identifier.citationShmakov, Sergey et al. “Discovery and Functional Characterization of Diverse Class 2 CRISPR-Cas Systems.” Molecular Cell 60, 3 (November 2015): 385–397 © 2015 Elsevieren_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biological Engineeringen_US
dc.contributor.departmentMcGovern Institute for Brain Research at MITen_US
dc.contributor.mitauthorAbudayyeh, Omar Osama
dc.contributor.mitauthorGootenberg, Jonathan S
dc.contributor.mitauthorJoung, Julia
dc.contributor.mitauthorKonermann, Silvana M
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
dc.date.updated2017-12-13T13:48:06Z
dspace.orderedauthorsShmakov, Sergey; Abudayyeh, Omar O.; Makarova, Kira S.; Wolf, Yuri I.; Gootenberg, Jonathan S.; Semenova, Ekaterina; Minakhin, Leonid; Joung, Julia; Konermann, Silvana; Severinov, Konstantin; Zhang, Feng; Koonin, Eugene V.en_US
dspace.embargo.termsNen_US
dc.identifier.orcidhttps://orcid.org/0000-0002-7979-3220
dc.identifier.orcidhttps://orcid.org/0000-0001-6656-5002
dc.identifier.orcidhttps://orcid.org/0000-0001-7915-1685
dc.identifier.orcidhttps://orcid.org/0000-0003-2782-2509
mit.licensePUBLISHER_CCen_US
mit.metadata.statusComplete


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