Adr1 and Cat8 mediate coactivator recruitment and chromatin remodeling at glucose-regulated genes.

Adr1 and Cat8 co-regulate numerous glucose-repressed genes in S. cerevisiae, presenting a unique opportunity to explore their individual roles in coactivator recruitment, chromatin remodeling, and transcription.We determined the individual contributions of Cat8 and Adr1 on the expression of a cohort...

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Main Authors: Rhiannon K Biddick, G Lynn Law, Elton T Young
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2008-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC2175534?pdf=render
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spelling doaj-0a453ce283924b56b4af8a48293cd26b2020-11-25T01:24:00ZengPublic Library of Science (PLoS)PLoS ONE1932-62032008-01-0131e143610.1371/journal.pone.0001436Adr1 and Cat8 mediate coactivator recruitment and chromatin remodeling at glucose-regulated genes.Rhiannon K BiddickG Lynn LawElton T YoungAdr1 and Cat8 co-regulate numerous glucose-repressed genes in S. cerevisiae, presenting a unique opportunity to explore their individual roles in coactivator recruitment, chromatin remodeling, and transcription.We determined the individual contributions of Cat8 and Adr1 on the expression of a cohort of glucose-repressed genes and found three broad categories: genes that need both activators for full derepression, genes that rely mostly on Cat8 and genes that require only Adr1. Through combined expression and recruitment data, along with analysis of chromatin remodeling at two of these genes, ADH2 and FBP1, we clarified how these activators achieve this wide range of co-regulation. We find that Adr1 and Cat8 are not intrinsically different in their abilities to recruit coactivators but rather, promoter context appears to dictate which activator is responsible for recruitment to specific genes. These promoter-specific contributions are also apparent in the chromatin remodeling that accompanies derepression: ADH2 requires both Adr1 and Cat8, whereas, at FBP1, significant remodeling occurs with Cat8 alone. Although over-expression of Adr1 can compensate for loss of Cat8 at many genes in terms of both activation and chromatin remodeling, this over-expression cannot complement all of the cat8Delta phenotypes.Thus, at many of the glucose-repressed genes, Cat8 and Adr1 appear to have interchangeable roles and promoter architecture may dictate the roles of these activators.http://europepmc.org/articles/PMC2175534?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Rhiannon K Biddick
G Lynn Law
Elton T Young
spellingShingle Rhiannon K Biddick
G Lynn Law
Elton T Young
Adr1 and Cat8 mediate coactivator recruitment and chromatin remodeling at glucose-regulated genes.
PLoS ONE
author_facet Rhiannon K Biddick
G Lynn Law
Elton T Young
author_sort Rhiannon K Biddick
title Adr1 and Cat8 mediate coactivator recruitment and chromatin remodeling at glucose-regulated genes.
title_short Adr1 and Cat8 mediate coactivator recruitment and chromatin remodeling at glucose-regulated genes.
title_full Adr1 and Cat8 mediate coactivator recruitment and chromatin remodeling at glucose-regulated genes.
title_fullStr Adr1 and Cat8 mediate coactivator recruitment and chromatin remodeling at glucose-regulated genes.
title_full_unstemmed Adr1 and Cat8 mediate coactivator recruitment and chromatin remodeling at glucose-regulated genes.
title_sort adr1 and cat8 mediate coactivator recruitment and chromatin remodeling at glucose-regulated genes.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2008-01-01
description Adr1 and Cat8 co-regulate numerous glucose-repressed genes in S. cerevisiae, presenting a unique opportunity to explore their individual roles in coactivator recruitment, chromatin remodeling, and transcription.We determined the individual contributions of Cat8 and Adr1 on the expression of a cohort of glucose-repressed genes and found three broad categories: genes that need both activators for full derepression, genes that rely mostly on Cat8 and genes that require only Adr1. Through combined expression and recruitment data, along with analysis of chromatin remodeling at two of these genes, ADH2 and FBP1, we clarified how these activators achieve this wide range of co-regulation. We find that Adr1 and Cat8 are not intrinsically different in their abilities to recruit coactivators but rather, promoter context appears to dictate which activator is responsible for recruitment to specific genes. These promoter-specific contributions are also apparent in the chromatin remodeling that accompanies derepression: ADH2 requires both Adr1 and Cat8, whereas, at FBP1, significant remodeling occurs with Cat8 alone. Although over-expression of Adr1 can compensate for loss of Cat8 at many genes in terms of both activation and chromatin remodeling, this over-expression cannot complement all of the cat8Delta phenotypes.Thus, at many of the glucose-repressed genes, Cat8 and Adr1 appear to have interchangeable roles and promoter architecture may dictate the roles of these activators.
url http://europepmc.org/articles/PMC2175534?pdf=render
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