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dc.contributor.authorCao, Bo
dc.contributor.authorCheng, Qiuxiang
dc.contributor.authorGu, Chen
dc.contributor.authorYao, Fen
dc.contributor.authorDeMott, Michael S.
dc.contributor.authorZheng, Xiaoqing
dc.contributor.authorDeng, Zixin
dc.contributor.authorDedon, Peter C.
dc.contributor.authorYou, Delin
dc.date.accessioned2015-10-15T13:41:39Z
dc.date.available2015-10-15T13:41:39Z
dc.date.issued2014-07
dc.identifier.issn0950382X
dc.identifier.issn1365-2958
dc.identifier.urihttp://hdl.handle.net/1721.1/99340
dc.description.abstractProkaryotes protect their genomes from foreign DNA with a diversity of defence mechanisms, including a widespread restriction–modification (R–M) system involving phosphorothioate (PT) modification of the DNA backbone. Unlike classical R–M systems, highly partial PT modification of consensus motifs in bacterial genomes suggests an unusual mechanism of PT-dependent restriction. In Salmonella enterica, PT modification is mediated by four genes dptB–E, while restriction involves additional three genes dptF–H. Here, we performed a series of studies to characterize the PT-dependent restriction, and found that it presented several features distinct with traditional R–M systems. The presence of restriction genes in a PT-deficient mutant was not lethal, but instead resulted in several pathological phenotypes. Subsequent transcriptional profiling revealed the expression of > 600 genes was affected by restriction enzymes in cells lacking PT, including induction of bacteriophage, SOS response and DNA repair-related genes. These transcriptional responses are consistent with the observation that restriction enzymes caused extensive DNA cleavage in the absence of PT modifications in vivo. However, overexpression of restriction genes was lethal to the host in spite of the presence PT modifications. These results point to an unusual mechanism of PT-dependent DNA cleavage by restriction enzymes in the face of partial PT modification.en_US
dc.description.sponsorshipNational Natural Science Foundation (China) (Grant 31170085)en_US
dc.description.sponsorshipNational Natural Science Foundation (China) (Grant 31070058)en_US
dc.description.sponsorshipMinistry of Science and Technology of the People's Republic of China (973 and 863 Programs)en_US
dc.description.sponsorshipChina Scholarship Councilen_US
dc.description.sponsorshipNational Science Foundation (U.S.) (Grant CHE-1019990)en_US
dc.description.sponsorshipShanghai Municipal Council of Science and Technology. Shanghai Pujiang Program (Grant 12PJD021)en_US
dc.language.isoen_US
dc.publisherWiley Blackwellen_US
dc.relation.isversionofhttp://dx.doi.org/10.1111/mmi.12692en_US
dc.rightsCreative Commons Attribution-Noncommercial-Share Alikeen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/en_US
dc.sourcePMCen_US
dc.titlePathological phenotypes and in vivo DNA cleavage by unrestrained activity of a phosphorothioate-based restriction system in Salmonellaen_US
dc.typeArticleen_US
dc.identifier.citationCao, Bo, Qiuxiang Cheng, Chen Gu, Fen Yao, Michael S. DeMott, Xiaoqing Zheng, Zixin Deng, Peter C. Dedon, and Delin You. “ Pathological Phenotypes and in Vivo DNA Cleavage by Unrestrained Activity of a Phosphorothioate-Based Restriction System in S Almonella .” Molecular Microbiology 93, no. 4 (July 23, 2014): 776–785.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Center for Environmental Health Sciencesen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biological Engineeringen_US
dc.contributor.mitauthorCao, Boen_US
dc.contributor.mitauthorGu, Chenen_US
dc.contributor.mitauthorDeMott, Michael S.en_US
dc.contributor.mitauthorDedon, Peter C.en_US
dc.relation.journalMolecular Microbiologyen_US
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsCao, Bo; Cheng, Qiuxiang; Gu, Chen; Yao, Fen; DeMott, Michael S.; Zheng, Xiaoqing; Deng, Zixin; Dedon, Peter C.; You, Delinen_US
dc.identifier.orcidhttps://orcid.org/0000-0003-1615-1578
dc.identifier.orcidhttps://orcid.org/0000-0003-0011-3067
dc.identifier.orcidhttps://orcid.org/0000-0001-9920-2080
mit.licenseOPEN_ACCESS_POLICYen_US
mit.metadata.statusComplete


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