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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
          0404511
          7473
          Science
          Science
          Science (New York, N.Y.)
          0036-8075
          1095-9203
          3 February 2021
          28 August 2020
          23 March 2021
          : 369
          : 6507
          : 1077-1084
          Affiliations
          [1 ]Howard Hughes Medical Institute, Cambridge, MA 02139, USA
          [2 ]Broad Institute of MIT and Harvard, Cambridge, Massachusetts 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
          [6 ]Department of Brain and Cognitive Sciences, Massachusetts Institute of Technology, Cambridge, MA 02139, USA
          Author notes
          [* ]Correspondence should be addressed to zhang@ 123456broadinstitute.org (F.Z.).

          Author contributions: L.G. and F.Z. conceived of the project. L.G. and H.A.-T. performed defense island analysis. L.G. cloned defense systems and performed transcriptome sequencing. L.G. performed plaque assays with assistance from F.B., M.S., and J.K. L.G. and F.B. performed bacterial density and phage fragmentation assays. H.A.-T. performed phylogenetic distribution and prophage analysis. L.G., H.A.-T., F.B., K.S.M., J.L.S.-B., Y.I.W., E.V.K., and F.Z. analyzed data. F.Z. supervised the research and experimental design. L.G., H.A.-T., E.V.K., and F.Z. wrote and revised the manuscript with input from all authors.

          Article
          PMC7985843 PMC7985843 7985843 nihpa1667515
          10.1126/science.aba0372
          7985843
          32855333
          02c6da03-d068-4f61-ac4f-678cc4848554
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