Diverse enzymatic activities mediate antiviral immunity in prokaryotes

Author:

Gao Linyi123ORCID,Altae-Tran Han123ORCID,Böhning Francisca12ORCID,Makarova Kira S.4ORCID,Segel Michael12356,Schmid-Burgk Jonathan L.12356ORCID,Koob Jeremy12ORCID,Wolf Yuri I.4ORCID,Koonin Eugene V.4ORCID,Zhang Feng12356ORCID

Affiliation:

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.

Abstract

Prokaryotic enzymes for viral defense The arms race between prokaryotes and viruses provides a strong evolutionary force to create diverse enzymatic activities that mediate antiviral immune responses. These immune components often cluster together in the host genomes, leading to expanded defense systems. Taking advantage of the evolutionary modularity of defense systems, Gao et al. bioinformatically predicted defense genes in most available bacterial and archaeal genomes. In addition, they reconstituted the newly identified systems in Escherichia coli and verified their defense functions against specific bacteriophages. In particular, they characterized defense functions for several predicted nucleoside triphosphatases. Science , this issue p. 1077

Funder

National Institutes of Health

Howard Hughes Medical Institute

U.S. Department of Health and Human Services

G Harold and Leila Y. Mathers Foundation

New York Stem Cell Foundation

Edward Mallinckrodt, Jr. Foundation

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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