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dc.rights.licenseopenen_US
dc.contributor.authorTANTALE, Katjana
dc.contributor.authorGARCIA-OLIVER, Encar
dc.contributor.authorROBERT, Marie-Cécile
dc.contributor.authorL'HOSTIS, Adèle
dc.contributor.authorYANG, Yueyuxiao
dc.contributor.authorTSANOV, Nikolay
dc.contributor.authorTOPNO, Rachel
dc.contributor.authorGOSTAN, Thierry
dc.contributor.authorKOZULIC-PIRHER, Alja
dc.contributor.authorBASU-SHRIVASTAVA, Meenakshi
dc.contributor.authorMUKHERJEE, Kamalika
dc.contributor.authorSLANINOVA, Vera
dc.contributor.authorANDRAU, Jean-Christophe
dc.contributor.authorMUELLER, Florian
hal.structure.identifierMicrobiologie Fondamentale et Pathogénicité [MFP]
dc.contributor.authorBASYUK, Eugenia
dc.contributor.authorRADULESCU, Ovidiu
dc.contributor.authorBERTRAND, Edouard
dc.date.accessioned2024-10-31T08:20:46Z
dc.date.available2024-10-31T08:20:46Z
dc.date.issued2021-07-23
dc.identifier.issn2041-1723en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/203065
dc.description.abstractEnPromoter-proximal pausing of RNA polymerase II is a key process regulating gene expression. In latent HIV-1 cells, it prevents viral transcription and is essential for latency maintenance, while in acutely infected cells the viral factor Tat releases paused polymerase to induce viral expression. Pausing is fundamental for HIV-1, but how it contributes to bursting and stochastic viral reactivation is unclear. Here, we performed single molecule imaging of HIV-1 transcription. We developed a quantitative analysis method that manages multiple time scales from seconds to days and that rapidly fits many models of promoter dynamics. We found that RNA polymerases enter a long-lived pause at latent HIV-1 promoters (>20 minutes), thereby effectively limiting viral transcription. Surprisingly and in contrast to current models, pausing appears stochastic and not obligatory, with only a small fraction of the polymerases undergoing long-lived pausing in absence of Tat. One consequence of stochastic pausing is that HIV-1 transcription occurs in bursts in latent cells, thereby facilitating latency exit and providing a rationale for the stochasticity of viral rebounds.
dc.language.isoENen_US
dc.rightsAttribution 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/us/*
dc.subject.enAlgorithms
dc.subject.enDNA-Directed RNA Polymerases
dc.subject.enGene Expression Regulation
dc.subject.enViral
dc.subject.enHIV Infections
dc.subject.enHIV-1
dc.subject.enHeLa Cells
dc.subject.enHumans
dc.subject.enModels
dc.subject.enGenetic
dc.subject.enPromoter Regions
dc.subject.enGenetic
dc.subject.enStochastic Processes
dc.subject.enTime Factors
dc.subject.enVirus Activation
dc.subject.enVirus Latency
dc.subject.entat Gene Products
dc.subject.enHuman Immunodeficiency Virus
dc.title.enStochastic pausing at latent HIV-1 promoters generates transcriptional bursting.
dc.title.alternativeNat Communen_US
dc.typeArticle de revueen_US
dc.identifier.doi10.1038/s41467-021-24462-5en_US
dc.subject.halSciences du Vivant [q-bio]/Microbiologie et Parasitologieen_US
dc.identifier.pubmed34301927en_US
bordeaux.journalNature Communicationsen_US
bordeaux.page4503en_US
bordeaux.volume12en_US
bordeaux.hal.laboratoriesMFP (Laboratoire Microbiologie Fondamentale et Pathogénicité) - UMR 5234en_US
bordeaux.issue1en_US
bordeaux.institutionCNRSen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
bordeaux.import.sourcepubmed
hal.popularnonen_US
hal.audienceInternationaleen_US
hal.exportfalse
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=Nature%20Communications&rft.date=2021-07-23&rft.volume=12&rft.issue=1&rft.spage=4503&rft.epage=4503&rft.eissn=2041-1723&rft.issn=2041-1723&rft.au=TANTALE,%20Katjana&GARCIA-OLIVER,%20Encar&ROBERT,%20Marie-C%C3%A9cile&L'HOSTIS,%20Ad%C3%A8le&YANG,%20Yueyuxiao&rft.genre=article


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