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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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2015
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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. |
format | Online Article Text |
id | pubmed-4664762 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
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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