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dc.rights.licenseopenen_US
hal.structure.identifierMicrobiologie Fondamentale et Pathogénicité [MFP]
dc.contributor.authorLAGADEC, Floriane
dc.contributor.authorSINGH, Parmit K
hal.structure.identifierMicrobiologie Fondamentale et Pathogénicité [MFP]
dc.contributor.authorCALMELS, Christina
hal.structure.identifierMicrobiologie Fondamentale et Pathogénicité [MFP]
dc.contributor.authorLAPAILLERIE, Delphine
dc.contributor.authorLINDEMANN, Dirk
hal.structure.identifierMicrobiologie Fondamentale et Pathogénicité [MFP]
dc.contributor.authorPARISSI, Vincent
dc.contributor.authorCHEREPANOV, Peter
dc.contributor.authorENGELMAN, Alan N
hal.structure.identifierMicrobiologie Fondamentale et Pathogénicité [MFP]
dc.contributor.authorLESBATS, Paul
dc.date.accessioned2025-06-02T07:50:16Z
dc.date.available2025-06-02T07:50:16Z
dc.date.issued2025-05-22
dc.identifier.issn1362-4962en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/206804
dc.description.abstractEnSelection of a suitable chromatin environment during retroviral integration is a tightly regulated process. Most retroviruses, including spumaretroviruses, require mitosis for nuclear entry. However, whether intrinsic chromatin dynamics during mitosis modulates retroviral genome invasion is unknown. Previous work uncovered critical interactions of prototype foamy virus (PFV) Gag with nucleosomes via a highly conserved arginine anchor residue. Yet, the regulation of Gag-chromatin interaction and its functional consequences for spumaretrovirus biology remain obscure. Here, we investigated the kinetics of chromatin binding by Gag during mitosis and proviral integration in synchronized cells. We showed that alteration of Gag affinity for nucleosome binding induced untimely chromatin tethering during mitosis, decreased infectivity, and redistributed viral integration sites to markers associated with late replication timing of chromosomes. Mutant Gag proteins were, moreover, defective in their ability to displace the histone H4 tail from the nucleosome acidic patch of highly condensed chromatin. These data indicate that the chromatin landscape during Gag-nucleosome interactions is important for PFV integration site selection and that spumaretroviruses evolved high-affinity chromatin binding to overcome early mitosis chromatin condensation.
dc.language.isoENen_US
dc.rightsAttribution 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/us/*
dc.subject.enMitosis
dc.subject.enSpumavirus
dc.subject.enVirus Integration
dc.subject.enChromatin
dc.subject.enHumans
dc.subject.enNucleosomes
dc.subject.enGene Products
dc.subject.engag
dc.subject.enHistones
dc.subject.enAnimals
dc.subject.enProtein Binding
dc.title.enTimed chromatin invasion during mitosis governs prototype foamy virus integration site selection and infectivity.
dc.title.alternativeNucleic Acids Resen_US
dc.typeArticle de revueen_US
dc.identifier.doi10.1093/nar/gkaf449en_US
dc.subject.halSciences du Vivant [q-bio]/Microbiologie et Parasitologieen_US
dc.identifier.pubmed40448500en_US
bordeaux.journalNucleic Acids Researchen_US
bordeaux.volume53en_US
bordeaux.hal.laboratoriesMFP (Laboratoire Microbiologie Fondamentale et Pathogénicité) - UMR 5234en_US
bordeaux.issue10en_US
bordeaux.institutionCNRSen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
bordeaux.import.sourcepubmed
hal.identifierhal-05092464
hal.version1
hal.date.transferred2025-06-02T07:50:21Z
hal.popularnonen_US
hal.audienceInternationaleen_US
hal.exporttrue
workflow.import.sourcepubmed
dc.rights.ccPas de Licence CCen_US
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Nucleic%20Acids%20Research&rft.date=2025-05-22&rft.volume=53&rft.issue=10&rft.eissn=1362-4962&rft.issn=1362-4962&rft.au=LAGADEC,%20Floriane&SINGH,%20Parmit%20K&CALMELS,%20Christina&LAPAILLERIE,%20Delphine&LINDEMANN,%20Dirk&rft.genre=article


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