Fiche publication
Date publication
septembre 2017
Journal
Molecular cell
Auteurs
Membres identifiés du Cancéropôle Est :
Dr DEVYS Didier
,
Dr TORA Laszlo
Tous les auteurs :
Baptista T, Grünberg S, Minoungou N, Koster MJE, Timmers HTM, Hahn S, Devys D, Tora L
Lien Pubmed
Résumé
Prior studies suggested that SAGA and TFIID are alternative factors that promote RNA polymerase II transcription, with about 10% of genes in S. cerevisiae dependent on SAGA. We reassessed the role of SAGA by mapping its genome-wide location and role in global transcription in budding yeast. We find that SAGA maps to the UAS elements of most genes, overlapping with Mediator binding and irrespective of previous designations of SAGA- or TFIID-dominated genes. Disruption of SAGA through mutation or rapid subunit depletion reduces transcription from nearly all genes, measured by newly synthesized RNA. We also find that the acetyltransferase Gcn5 synergizes with Spt3 to promote global transcription and that Spt3 functions to stimulate TBP recruitment at all tested genes. Our data demonstrate that SAGA acts as a general cofactor required for essentially all RNA polymerase II transcription and is not consistent with the previous classification of SAGA- and TFIID-dominated genes.
Mots clés
RNA polymerase II, SAGA complex, TATA box, TFIID complex, coactivator, transcription initiation
Référence
Mol. Cell. 2017 Sep;:
