ISWI and CHD chromatin remodelers bind promoters but act in gene bodies.

ATP-dependent nucleosome remodelers influence genetic processes by altering nucleosome occupancy, positioning, and composition. In vitro, Saccharomyces cerevisiae ISWI and CHD remodelers require ∼30-85 bp of extranucleosomal DNA to reposition nucleosomes, but linker DNA in S. cerevisiae averages <...

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Main Authors: Gabriel E Zentner, Toshio Tsukiyama, Steven Henikoff
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS Genetics
Online Access:http://europepmc.org/articles/PMC3585014?pdf=render
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spelling doaj-14dd11e84ffb4db0bb6005d0815fa5242020-11-24T22:05:32ZengPublic Library of Science (PLoS)PLoS Genetics1553-73901553-74042013-01-0192e100331710.1371/journal.pgen.1003317ISWI and CHD chromatin remodelers bind promoters but act in gene bodies.Gabriel E ZentnerToshio TsukiyamaSteven HenikoffATP-dependent nucleosome remodelers influence genetic processes by altering nucleosome occupancy, positioning, and composition. In vitro, Saccharomyces cerevisiae ISWI and CHD remodelers require ∼30-85 bp of extranucleosomal DNA to reposition nucleosomes, but linker DNA in S. cerevisiae averages <20 bp. To address this discrepancy between in vitro and in vivo observations, we have mapped the genomic distributions of the yeast Isw1, Isw2, and Chd1 remodelers at base-pair resolution on native chromatin. Although these remodelers act in gene bodies, we find that they are also highly enriched at nucleosome-depleted regions (NDRs), where they bind to extended regions of DNA adjacent to particular transcription factors. Surprisingly, catalytically inactive remodelers show similar binding patterns. We find that remodeler occupancy at NDRs and gene bodies is associated with nucleosome turnover and transcriptional elongation rate, suggesting that remodelers act on regions of transient nucleosome unwrapping or depletion within gene bodies subsequent to transcriptional elongation.http://europepmc.org/articles/PMC3585014?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Gabriel E Zentner
Toshio Tsukiyama
Steven Henikoff
spellingShingle Gabriel E Zentner
Toshio Tsukiyama
Steven Henikoff
ISWI and CHD chromatin remodelers bind promoters but act in gene bodies.
PLoS Genetics
author_facet Gabriel E Zentner
Toshio Tsukiyama
Steven Henikoff
author_sort Gabriel E Zentner
title ISWI and CHD chromatin remodelers bind promoters but act in gene bodies.
title_short ISWI and CHD chromatin remodelers bind promoters but act in gene bodies.
title_full ISWI and CHD chromatin remodelers bind promoters but act in gene bodies.
title_fullStr ISWI and CHD chromatin remodelers bind promoters but act in gene bodies.
title_full_unstemmed ISWI and CHD chromatin remodelers bind promoters but act in gene bodies.
title_sort iswi and chd chromatin remodelers bind promoters but act in gene bodies.
publisher Public Library of Science (PLoS)
series PLoS Genetics
issn 1553-7390
1553-7404
publishDate 2013-01-01
description ATP-dependent nucleosome remodelers influence genetic processes by altering nucleosome occupancy, positioning, and composition. In vitro, Saccharomyces cerevisiae ISWI and CHD remodelers require ∼30-85 bp of extranucleosomal DNA to reposition nucleosomes, but linker DNA in S. cerevisiae averages <20 bp. To address this discrepancy between in vitro and in vivo observations, we have mapped the genomic distributions of the yeast Isw1, Isw2, and Chd1 remodelers at base-pair resolution on native chromatin. Although these remodelers act in gene bodies, we find that they are also highly enriched at nucleosome-depleted regions (NDRs), where they bind to extended regions of DNA adjacent to particular transcription factors. Surprisingly, catalytically inactive remodelers show similar binding patterns. We find that remodeler occupancy at NDRs and gene bodies is associated with nucleosome turnover and transcriptional elongation rate, suggesting that remodelers act on regions of transient nucleosome unwrapping or depletion within gene bodies subsequent to transcriptional elongation.
url http://europepmc.org/articles/PMC3585014?pdf=render
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