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dc.contributor.authorShmakov, S.
dc.contributor.authorMakarova, K. S.
dc.contributor.authorSemenova, E.
dc.contributor.authorMinakhin, L.
dc.contributor.authorSeverinov, K.
dc.contributor.authorKoonin, E. V.
dc.contributor.authorRegev, Aviv
dc.contributor.authorGootenberg, Jonathan S
dc.contributor.authorKonermann, Silvana M
dc.contributor.authorJoung, Julia
dc.contributor.authorSlaymaker, Ian
dc.contributor.authorCox, David Benjamin Turitz
dc.contributor.authorLander, Eric Steven
dc.contributor.authorZhang, Feng
dc.contributor.authorAbudayyeh, Omar O.
dc.date.accessioned2016-12-09T20:58:39Z
dc.date.available2016-12-09T20:58:39Z
dc.date.issued2016-08
dc.date.submitted2016-03
dc.identifier.issn0036-8075
dc.identifier.issn1095-9203
dc.identifier.urihttp://hdl.handle.net/1721.1/105791
dc.description.abstractThe clustered regularly interspaced short palindromic repeat (CRISPR)–CRISPR-associated genes (Cas) adaptive immune system defends microbes against foreign genetic elements via DNA or RNA-DNA interference. We characterize the class 2 type VI CRISPR-Cas effector C2c2 and demonstrate its RNA-guided ribonuclease function. C2c2 from the bacterium Leptotrichia shahii provides interference against RNA phage. In vitro biochemical analysis shows that C2c2 is guided by a single CRISPR RNA and can be programmed to cleave single-stranded RNA targets carrying complementary protospacers. In bacteria, C2c2 can be programmed to knock down specific mRNAs. Cleavage is mediated by catalytic residues in the two conserved Higher Eukaryotes and Prokaryotes Nucleotide-binding (HEPN) domains, mutations of which generate catalytically inactive RNA-binding proteins. These results broaden our understanding of CRISPR-Cas systems and suggest that C2c2 can be used to develop new RNA-targeting tools.en_US
dc.description.sponsorshipUnited States. Dept. of Energy (Computational Science Graduate Fellowship)en_US
dc.description.sponsorshipMassachusetts Institute of Technology. Simons Center for the Social Brainen_US
dc.description.sponsorshipNational Institute of General Medical Sciences (U.S.) (Award T32GM007753)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (National Institute of Mental Health (U.S.) Grants 5DP1-MH100706 and 1R01-MH110049)en_US
dc.description.sponsorshipNational Science Foundation (U.S.)en_US
dc.description.sponsorshipNew York Stem Cell Foundationen_US
dc.description.sponsorshipSimons Foundationen_US
dc.description.sponsorshipPaul G. Allen Family Foundationen_US
dc.description.sponsorshipVallee Foundationen_US
dc.description.sponsorshipPoitras Foundationen_US
dc.description.sponsorshipRobert Metcalfeen_US
dc.description.sponsorshipDavid R. Chengen_US
dc.language.isoen_US
dc.publisherAmerican Association for the Advancement of Science (AAAS)en_US
dc.relation.isversionofhttp://dx.doi.org/10.1126/science.aaf5573en_US
dc.rightsArticle is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.en_US
dc.sourcePMCen_US
dc.titleC2c2 is a single-component programmable RNA-guided RNA-targeting CRISPR effectoren_US
dc.typeArticleen_US
dc.identifier.citationAbudayyeh, O. O. et al. “C2c2 Is a Single-Component Programmable RNA-Guided RNA-Targeting CRISPR Effector.” Science 353.6299 (2016): aaf5573-aaf5573.en_US
dc.contributor.departmentHarvard University--MIT Division of Health Sciences and Technologyen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biological Engineeringen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biologyen_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.mitauthorRegev, Aviv
dc.contributor.mitauthorAbudayyeh, Omar Osama
dc.contributor.mitauthorGootenberg, Jonathan S
dc.contributor.mitauthorKonermann, Silvana M
dc.contributor.mitauthorJoung, Julia
dc.contributor.mitauthorSlaymaker, Ian
dc.contributor.mitauthorCox, David Benjamin Turitz
dc.contributor.mitauthorLander, Eric Steven
dc.contributor.mitauthorZhang, Feng
dc.relation.journalScienceen_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.orderedauthorsAbudayyeh, O. O.; Gootenberg, J. S.; Konermann, S.; Joung, J.; Slaymaker, I. M.; Cox, D. B. T.; Shmakov, S.; Makarova, K. S.; Semenova, E.; Minakhin, L.; Severinov, K.; Regev, A.; Lander, E. S.; Koonin, E. V.; Zhang, F.en_US
dspace.embargo.termsNen_US
dc.identifier.orcidhttps://orcid.org/0000-0001-8567-2049
dc.identifier.orcidhttps://orcid.org/0000-0002-7979-3220
dc.identifier.orcidhttps://orcid.org/0000-0001-7915-1685
dc.identifier.orcidhttps://orcid.org/0000-0001-6656-5002
dc.identifier.orcidhttps://orcid.org/0000-0001-8794-2137
dc.identifier.orcidhttps://orcid.org/0000-0001-7626-4254
dc.identifier.orcidhttps://orcid.org/0000-0003-2782-2509
mit.licensePUBLISHER_POLICYen_US


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