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      Diverse enzymatic activities mediate antiviral immunity in prokaryotes.

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          Abstract

          Bacteria and archaea are frequently attacked by viruses and other mobile genetic elements and rely on dedicated antiviral defense systems, such as restriction endonucleases and CRISPR, to survive. The enormous diversity of viruses suggests that more types of defense systems exist than are currently known. By systematic defense gene prediction and heterologous reconstitution, here we discover 29 widespread antiviral gene cassettes, collectively present in 32% of all sequenced bacterial and archaeal genomes, that mediate protection against specific bacteriophages. These systems incorporate enzymatic activities not previously implicated in antiviral defense, including RNA editing and retron satellite DNA synthesis. In addition, we computationally predict a diverse set of other putative defense genes that remain to be characterized. These results highlight an immense array of molecular functions that microbes use against viruses.

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          Author and article information

          Journal
          Science
          Science (New York, N.Y.)
          American Association for the Advancement of Science (AAAS)
          1095-9203
          0036-8075
          August 28 2020
          : 369
          : 6507
          Affiliations
          [1 ] Howard Hughes Medical Institute, Cambridge, MA 02139, USA.
          [2 ] Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA.
          [3 ] Department of Biological Engineering, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.
          [4 ] National Center for Biotechnology Information, National Library of Medicine, National Institutes of Health, Bethesda, MD 20894, USA.
          [5 ] McGovern Institute for Brain Research, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.
          [6 ] Department of Brain and Cognitive Sciences, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.
          [7 ] Howard Hughes Medical Institute, Cambridge, MA 02139, USA. zhang@broadinstitute.org.
          Article
          369/6507/1077 NIHMS1667515
          10.1126/science.aba0372
          7985843
          32855333
          02c6da03-d068-4f61-ac4f-678cc4848554
          Copyright © 2020 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works.
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