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dc.rights.licenseopenen_US
dc.contributor.authorFLORINI, Francesca
dc.contributor.authorNAGULESWARAN, Arunasalam
dc.contributor.authorGHARIB, Walid
hal.structure.identifierMicrobiologie Fondamentale et Pathogénicité [MFP]
dc.contributor.authorBRINGAUD, Frédéric
dc.contributor.authorRODITI, Isabel
dc.date.accessioned2023-06-14T10:39:47Z
dc.date.available2023-06-14T10:39:47Z
dc.date.issued2019
dc.identifier.issn0305-1048en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/182683
dc.description.abstractEnThe path from DNA to RNA to protein in eukaryotes is guided by a series of factors linking transcription, mRNA export and translation. Many of these are conserved from yeast to humans. Trypanosomatids, which diverged early in the eukaryotic lineage, exhibit unusual features such as polycistronic transcription and trans-splicing of all messenger RNAs. They possess basal transcription factors, but lack recognisable orthologues of many factors required for transcription elongation and mRNA export. We show that retrotransposon hotspot (RHS) proteins fulfil some of these functions and that their depletion globally impairs nascent RNA synthesis by RNA polymerase II. Three sub-families are part of a coordinated process in which RHS6 is most closely associated with chromatin, RHS4 is part of the Pol II complex and RHS2 connects transcription with the translation machinery. In summary, our results show that the components of eukaryotic transcription are far from being universal, and reveal unsuspected plasticity in the course of evolution.
dc.language.isoENen_US
dc.rightsAttribution-NonCommercial 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by-nc/3.0/us/*
dc.title.enUnexpected diversity in eukaryotic transcription revealed by the retrotransposon hotspot family of Trypanosoma brucei
dc.typeArticle de revueen_US
dc.identifier.doi10.1093/nar/gky1255en_US
dc.subject.halSciences du Vivant [q-bio]/Microbiologie et Parasitologie/Parasitologieen_US
dc.subject.halSciences du Vivant [q-bio]/Biochimie, Biologie Moléculaire/Génomique, Transcriptomique et Protéomique [q-bio.GN]en_US
bordeaux.journalNucleic Acids Researchen_US
bordeaux.page1725-1739en_US
bordeaux.volume47en_US
bordeaux.hal.laboratoriesMFP (Laboratoire Microbiologie Fondamentale et Pathogénicité) - UMR 5234en_US
bordeaux.issue4en_US
bordeaux.institutionCNRSen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
bordeaux.import.sourcehal
hal.identifierhal-02347962
hal.version1
hal.exportfalse
workflow.import.sourcehal
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=2019&rft.volume=47&rft.issue=4&rft.spage=1725-1739&rft.epage=1725-1739&rft.eissn=0305-1048&rft.issn=0305-1048&rft.au=FLORINI,%20Francesca&NAGULESWARAN,%20Arunasalam&GHARIB,%20Walid&BRINGAUD,%20Fr%C3%A9d%C3%A9ric&RODITI,%20Isabel&rft.genre=article


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