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      Discovery and functional characterization of diverse Class 2 CRISPR-Cas systems

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          Abstract

          Microbial 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.

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          Author and article information

          Journal
          9802571
          20730
          Mol Cell
          Mol. Cell
          Molecular cell
          1097-2765
          1097-4164
          14 October 2015
          22 October 2015
          5 November 2015
          05 November 2016
          : 60
          : 3
          : 385-397
          Affiliations
          [1 ] Skolkovo Institute of Science and Technology, Skolkovo, 143025, Russia
          [2 ] National Center for Biotechnology Information, NLM, National Institutes of Health, Bethesda, MD 20894, USA
          [3 ] Broad Institute of MIT and Harvard, Cambridge, Massachusetts 02142, USA, McGovern Institute for Brain Research, Department of Brain and Cognitive Science, Department of Biological Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, USA
          [4 ] Waksman Institute for Microbiology, Rutgers, The State University of New Jersey, Piscataway, NJ 08854, USA
          [5 ] Institute of Molecular Genetics, Russian Academy of Sciences, Moscow, 123182, Russia
          Author notes
          [* ] Authors to whom correspondence should be addressed: koonin@ 123456ncbi.nlm.nih.gov ; zhang@ 123456broadinstitute.org
          [#]

          These authors made equal contributions to this work

          Article
          PMC4660269 PMC4660269 4660269 nihpa729607
          10.1016/j.molcel.2015.10.008
          4660269
          26593719
          a68c2e0e-8ae8-49ea-952c-dced6a08cdd4
          History
          Categories
          Article

          Cas9,RNA-seq,computational discovery pipeline,HEPN domain,RuvC-like endonuclease,PAM,tracrRNA,crRNA,Cpf1,CRISPR-Cas adaptive immunity

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