Sequence-directed action of RSC remodeler and pioneer factors positions +1 nucleosome to facilitate transcription
Slawomir KubikiD, Eoghan O’DuibhiriD, Wim J. de JongeiD, Stefano MattarocciiD, Benjamin AlbertiD, Jean-Luc FalconeiD, Maria Jessica BruzzoneiD, Frank C. P. HolstegeiD, David ShoreiD
Abstract
Accessible chromatin is important for RNA polymerase II recruitment and transcription initiation at eukaryotic promoters. We investigated the mechanistic links between promoter DNA sequence, nucleosome positioning and transcription. Our results indicate that precise positioning of the transcription start site-associated +1 nucleosome in yeast is critical for efficient TBP binding, and is driven by two key factors, the essential chromatin remodeler RSC and a small set of ubiquitous pioneer transcription factors. We find no evidence for recruitment of RSC by pioneer factors, but show instead that the strength and directionality of RSC action on nucleosomes depends upon the arrangement of two specific DNA motifs that promote its binding and nucleosome displacement activity at promoters. Thus, despite their widespread co-localization, RSC and pioneer factors predominantly act independently to generate accessible chromatin. Our results provide insight into how promoter DNA sequence instructs trans-acting factors to control nucleosome architecture and stimulate transcription initiation.
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