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dc.contributor.authorKoonin, Eugene V.
dc.contributor.authorZhang, Feng
dc.date.accessioned2017-12-12T16:46:11Z
dc.date.available2017-12-12T16:46:11Z
dc.date.issued2016-12
dc.identifier.issn0265-9247
dc.identifier.issn1521-1878
dc.identifier.urihttp://hdl.handle.net/1721.1/112717
dc.description.abstractHost-pathogen arms race is a universal, central aspect of the evolution of life. Most organisms evolved several distinct yet interacting strategies of anti-pathogen defense including resistance to parasite invasion, innate and adaptive immunity, and programmed cell death (PCD). The PCD is the means of last resort, a suicidal response to infection that is activated when resistance and immunity fail. An infected cell faces a decision between active defense and altruistic suicide or dormancy induction, depending on whether immunity is “deemed” capable of preventing parasite reproduction and consequent infection of other cells. In bacteria and archaea, immunity genes typically colocalize with PCD modules, such as toxins-antitoxins, suggestive of immunity-PCD coupling, likely mediated by shared proteins that sense damage and “predict” the outcome of infections. In type VI CRISPR-Cas systems, the same enzyme that inactivates the target RNA might execute cell suicide, in a case of ultimate integration of immunity and PCD.en_US
dc.publisherWiley Blackwellen_US
dc.relation.isversionofhttp://dx.doi.org/10.1002/bies.201600186en_US
dc.rightsCreative Commons Attribution-NonCommercial-NoDerivs Licenseen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/en_US
dc.sourceWileyen_US
dc.titleCoupling immunity and programmed cell suicide in prokaryotes: Life-or-death choicesen_US
dc.typeArticleen_US
dc.identifier.citationKoonin, Eugene V., and Zhang, Feng . “Coupling Immunity and Programmed Cell Suicide in Prokaryotes: Life-or-Death Choices.” BioEssays 39, 1 (November 2016): e201600186 © 2016 The Authorsen_US
dc.contributor.departmentHarvard University--MIT Division of Health Sciences and Technologyen_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.mitauthorZhang, Feng
dc.relation.journalBioEssaysen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2017-12-12T16:31:12Z
dspace.orderedauthorsKoonin, Eugene V.; Zhang, Fengen_US
dspace.embargo.termsNen_US
dc.identifier.orcidhttps://orcid.org/0000-0003-2782-2509
mit.licensePUBLISHER_CCen_US
mit.metadata.statusComplete


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