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dc.rights.licenseopenen_US
hal.structure.identifierMicrobiologie Fondamentale et Pathogénicité [MFP]
dc.contributor.authorLESBATS, Paul
hal.structure.identifierMicrobiologie Fondamentale et Pathogénicité [MFP]
dc.contributor.authorPARISSI, Vincent
dc.date.accessioned2023-11-08T08:26:25Z
dc.date.available2023-11-08T08:26:25Z
dc.date.issued2018-11-19
dc.identifier.issn2311-2638en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/184674
dc.description.abstractEnThe ability of retroviruses to integrate their genomes into host chromatin is a key step for the completion of their replication cycle. Selection of a suitable chromosomal integration site has been described as a hierarchical mechanism involving both cellular and viral proteins but the exact molecular determinants are still unclear. We recently showed that the spumaretrovirus prototype foamy virus (PFV) Gag protein is acting as a chromatin tether by interacting with the nucleosome acidic patch (Lesbats et al. 114(21)). Disruption of the nucleosome binding leads to a dramatic delocalization of both the viral particles and the integration sites accompanied with a reduction of integrated genes expression. These data show for the first time a direct interaction between retroviral structural proteins with the host chromosomes, and highlight their importance in the integration sites selection.
dc.language.isoENen_US
dc.rightsAttribution 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/us/*
dc.subject.enretrovirus
dc.subject.enintegration
dc.subject.ennucleosome
dc.subject.enchromatin-binding
dc.subject.enGag
dc.title.enRetroviral integration site selection: a running ?
dc.title.alternativeMicrob Cellen_US
dc.typeArticle de revueen_US
dc.identifier.doi10.15698/mic2018.12.663en_US
dc.subject.halSciences du Vivant [q-bio]/Microbiologie et Parasitologieen_US
dc.identifier.pubmed30533422en_US
bordeaux.journalMicrobial Cellen_US
bordeaux.page569-571en_US
bordeaux.volume5en_US
bordeaux.hal.laboratoriesMFP (Laboratoire Microbiologie Fondamentale et Pathogénicité) - UMR 5234en_US
bordeaux.issue12en_US
bordeaux.institutionCNRSen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
bordeaux.import.sourcepubmed
hal.identifierhal-04274654
hal.version1
hal.date.transferred2023-11-08T08:26:28Z
hal.popularnonen_US
hal.audienceInternationaleen_US
hal.exporttrue
workflow.import.sourcepubmed
dc.rights.ccPas de Licence CCen_US
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