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The conserved HDAC Rpd3 drives transcriptional quiescence in S. cerevisiae

Quiescence is a ubiquitous cell cycle stage conserved from microbes through humans and is essential to normal cellular function and response to changing environmental conditions. We recently reported a massive repressive event associated with quiescence in Saccharomyces cerevisiae, where Rpd3 establ...

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Detalles Bibliográficos
Autores principales: McKnight, Jeffrey N., Tsukiyama, Toshio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4664762/
https://www.ncbi.nlm.nih.gov/pubmed/26697386
http://dx.doi.org/10.1016/j.gdata.2015.10.008
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author McKnight, Jeffrey N.
Tsukiyama, Toshio
author_facet McKnight, Jeffrey N.
Tsukiyama, Toshio
author_sort McKnight, Jeffrey N.
collection PubMed
description Quiescence is a ubiquitous cell cycle stage conserved from microbes through humans and is essential to normal cellular function and response to changing environmental conditions. We recently reported a massive repressive event associated with quiescence in Saccharomyces cerevisiae, where Rpd3 establishes repressive chromatin structure that drives transcriptional shutoff [6]. Here, we describe in detail the experimental procedures, data collection, and data analysis related to our characterization of transcriptional quiescence in budding yeast (GEO: GSE67151). Our results provide a bona fide molecular event driven by widespread changes in chromatin structure through action of Rpd3 that distinguishes quiescence as a unique cell cycle stage in S. cerevisiae.
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spelling pubmed-46647622015-12-22 The conserved HDAC Rpd3 drives transcriptional quiescence in S. cerevisiae McKnight, Jeffrey N. Tsukiyama, Toshio Genom Data Data in Brief Quiescence is a ubiquitous cell cycle stage conserved from microbes through humans and is essential to normal cellular function and response to changing environmental conditions. We recently reported a massive repressive event associated with quiescence in Saccharomyces cerevisiae, where Rpd3 establishes repressive chromatin structure that drives transcriptional shutoff [6]. Here, we describe in detail the experimental procedures, data collection, and data analysis related to our characterization of transcriptional quiescence in budding yeast (GEO: GSE67151). Our results provide a bona fide molecular event driven by widespread changes in chromatin structure through action of Rpd3 that distinguishes quiescence as a unique cell cycle stage in S. cerevisiae. Elsevier 2015-10-17 /pmc/articles/PMC4664762/ /pubmed/26697386 http://dx.doi.org/10.1016/j.gdata.2015.10.008 Text en © 2015 The Authors. Published by Elsevier Inc. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Data in Brief
McKnight, Jeffrey N.
Tsukiyama, Toshio
The conserved HDAC Rpd3 drives transcriptional quiescence in S. cerevisiae
title The conserved HDAC Rpd3 drives transcriptional quiescence in S. cerevisiae
title_full The conserved HDAC Rpd3 drives transcriptional quiescence in S. cerevisiae
title_fullStr The conserved HDAC Rpd3 drives transcriptional quiescence in S. cerevisiae
title_full_unstemmed The conserved HDAC Rpd3 drives transcriptional quiescence in S. cerevisiae
title_short The conserved HDAC Rpd3 drives transcriptional quiescence in S. cerevisiae
title_sort conserved hdac rpd3 drives transcriptional quiescence in s. cerevisiae
topic Data in Brief
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4664762/
https://www.ncbi.nlm.nih.gov/pubmed/26697386
http://dx.doi.org/10.1016/j.gdata.2015.10.008
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