Mediator-Regulated Transcription through the +1 Nucleosome

Many genes are regulated at the level of a Pol II that is recruited to a nucleosome-free region upstream of the +1 nucleosome. How the Mediator coactivator complex, which functions at multiple steps, affects transcription through the promoter proximal region, including this nucleosome, remains large...

Full description

Saved in:
Bibliographic Details
Published inMolecular cell Vol. 48; no. 6; pp. 837 - 848
Main Authors Nock, Adam, Ascano, Janice M., Barrero, Maria J., Malik, Sohail
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 28.12.2012
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Many genes are regulated at the level of a Pol II that is recruited to a nucleosome-free region upstream of the +1 nucleosome. How the Mediator coactivator complex, which functions at multiple steps, affects transcription through the promoter proximal region, including this nucleosome, remains largely unaddressed. We have established a fully defined in vitro assay system to delineate mechanisms for Pol II transit across the +1 nucleosome. Our results reveal cooperative functions of multiple cofactors, particularly of Mediator and elongation factor SII, in transcribing into this nucleosome. This is achieved, in part, through an unusual activity of SII that alters the intrinsic catalytic properties of promoter-proximal Pol II and, in concert with the Mediator, leads to enhancement in transcription of nucleosomal DNA. Our data provide additional mechanistic bases for Mediator function after recruitment of Pol II and, potentially, for regulation of genes controlled via nucleosome-mediated promoter-proximal pausing. ► Development of an in vitro system to analyze transcription through a +1 nucleosome ► There is functional interplay between Mediator and chromatin cofactors ► SII induces reiterative oligomeric RNA synthesis by promoter-bound Pol II ► Mediator translates this activity of SII into processive transcription
Bibliography:http://dx.doi.org/10.1016/j.molcel.2012.10.009
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:1097-2765
1097-4164
DOI:10.1016/j.molcel.2012.10.009