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dc.contributor.authorMakarova, Kira S.
dc.contributor.authorvan der Oost, John
dc.contributor.authorKoonin, Eugene V.
dc.contributor.authorZetsche, Bernd
dc.contributor.authorGootenberg, Jonathan S
dc.contributor.authorAbudayyeh, Omar Osama
dc.contributor.authorSlaymaker, Ian
dc.contributor.authorEssletzbichler, Patrick
dc.contributor.authorVolz, Sara E.
dc.contributor.authorJoung, Julia
dc.contributor.authorRegev, Aviv
dc.contributor.authorZhang, Feng
dc.date.accessioned2016-12-07T21:38:01Z
dc.date.available2016-12-07T21:38:01Z
dc.date.issued2015-09
dc.date.submitted2015-09
dc.identifier.issn00928674
dc.identifier.urihttp://hdl.handle.net/1721.1/105747
dc.description.abstractThe microbial adaptive immune system CRISPR mediates defense against foreign genetic elements through two classes of RNA-guided nuclease effectors. Class 1 effectors utilize multiprotein complexes, whereas Class 2 effectors rely on single-component effector proteins such as the well-characterized Cas9. Here we report characterization of Cpf1, a putative Class 2 CRISPR effector. We demonstrate that Cpf1 mediates robust DNA interference with features distinct from Cas9. Cpf1 is a single RNA-guided endonuclease lacking tracrRNA, and it utilizes a T-rich protospacer adjacent motif. Moreover, Cpf1 cleaves DNA via a staggered DNA double stranded break. Out of 16 Cpf1-family proteins, we identified two candidate enzymes, from Acidominococcus and Lachnospiraceae, with efficient genome editing activity in human cells. Identifying this mechanism of interference broadens our understanding of CRISPR-Cas systems and advances their genome editing applications.en_US
dc.description.sponsorshipUnited States. Dept. of Energy (Computational Science Graduate Fellowship)en_US
dc.description.sponsorshipNational Institute of Mental Health (U.S.) (Grant 1DP1-MH100706)en_US
dc.description.sponsorshipPoitras Foundationen_US
dc.description.sponsorshipVallee Foundationen_US
dc.description.sponsorshipSimons Foundationen_US
dc.description.sponsorshipPaul G. Allen Family Foundationen_US
dc.description.sponsorshipNew York Stem Cell Foundationen_US
dc.description.sponsorshipRobert Metcalfeen_US
dc.description.sponsorshipDavid R. Chengen_US
dc.language.isoen_US
dc.publisherElsevieren_US
dc.relation.isversionofhttp://dx.doi.org/10.1016/j.cell.2015.09.038en_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.titleCpf1 Is a Single RNA-Guided Endonuclease of a Class 2 CRISPR-Cas Systemen_US
dc.typeArticleen_US
dc.identifier.citationZetsche, Bernd et al. “Cpf1 Is a Single RNA-Guided Endonuclease of a Class 2 CRISPR-Cas System.” Cell 163.3 (2015): 759–771.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 Brain and Cognitive Sciencesen_US
dc.contributor.departmentMcGovern Institute for Brain Research at MITen_US
dc.contributor.mitauthorZetsche, Bernd
dc.contributor.mitauthorGootenberg, Jonathan S
dc.contributor.mitauthorAbudayyeh, Omar Osama
dc.contributor.mitauthorSlaymaker, Ian
dc.contributor.mitauthorEssletzbichler, Patrick
dc.contributor.mitauthorVolz, Sara E.
dc.contributor.mitauthorJoung, Julia
dc.contributor.mitauthorRegev, Aviv
dc.contributor.mitauthorZhang, Feng
dc.relation.journalCellen_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.orderedauthorsZetsche, Bernd; Gootenberg, Jonathan S.; Abudayyeh, Omar O.; Slaymaker, Ian M.; Makarova, Kira S.; Essletzbichler, Patrick; Volz, Sara E.; Joung, Julia; van der Oost, John; Regev, Aviv; Koonin, Eugene V.; Zhang, Fengen_US
dspace.embargo.termsNen_US
dc.identifier.orcidhttps://orcid.org/0000-0002-7979-3220
dc.identifier.orcidhttps://orcid.org/0000-0001-8794-2137
dc.identifier.orcidhttps://orcid.org/0000-0001-6656-5002
dc.identifier.orcidhttps://orcid.org/0000-0001-8567-2049
dc.identifier.orcidhttps://orcid.org/0000-0003-2782-2509
mit.licensePUBLISHER_CCen_US


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