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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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Detalles Bibliográficos
Autores principales: Zentner, Gabriel E., Tsukiyama, Toshio, Henikoff, Steven
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3585014/
https://www.ncbi.nlm.nih.gov/pubmed/23468649
http://dx.doi.org/10.1371/journal.pgen.1003317
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author Zentner, Gabriel E.
Tsukiyama, Toshio
Henikoff, Steven
author_facet Zentner, Gabriel E.
Tsukiyama, Toshio
Henikoff, Steven
author_sort Zentner, Gabriel E.
collection PubMed
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.
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spelling pubmed-35850142013-03-06 ISWI and CHD Chromatin Remodelers Bind Promoters but Act in Gene Bodies Zentner, Gabriel E. Tsukiyama, Toshio Henikoff, Steven PLoS Genet Research Article 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. Public Library of Science 2013-02-28 /pmc/articles/PMC3585014/ /pubmed/23468649 http://dx.doi.org/10.1371/journal.pgen.1003317 Text en © 2013 Zentner et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Zentner, Gabriel E.
Tsukiyama, Toshio
Henikoff, Steven
ISWI and CHD Chromatin Remodelers Bind Promoters but Act in Gene Bodies
title 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_short 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
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3585014/
https://www.ncbi.nlm.nih.gov/pubmed/23468649
http://dx.doi.org/10.1371/journal.pgen.1003317
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