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High-Resolution Chromatin Dynamics during a Yeast Stress Response

Covalent histone modifications are highly conserved and play multiple roles in eukaryotic transcription regulation. Here, we mapped 26 histone modifications genome-wide in exponentially growing yeast and during a dramatic transcriptional reprogramming—the response to diamide stress. We extend prior...

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Autores principales: Weiner, Assaf, Hsieh, Tsung-Han S., Appleboim, Alon, Chen, Hsiuyi V., Rahat, Ayelet, Amit, Ido, Rando, Oliver J., Friedman, Nir
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cell Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4405355/
https://www.ncbi.nlm.nih.gov/pubmed/25801168
http://dx.doi.org/10.1016/j.molcel.2015.02.002
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author Weiner, Assaf
Hsieh, Tsung-Han S.
Appleboim, Alon
Chen, Hsiuyi V.
Rahat, Ayelet
Amit, Ido
Rando, Oliver J.
Friedman, Nir
author_facet Weiner, Assaf
Hsieh, Tsung-Han S.
Appleboim, Alon
Chen, Hsiuyi V.
Rahat, Ayelet
Amit, Ido
Rando, Oliver J.
Friedman, Nir
author_sort Weiner, Assaf
collection PubMed
description Covalent histone modifications are highly conserved and play multiple roles in eukaryotic transcription regulation. Here, we mapped 26 histone modifications genome-wide in exponentially growing yeast and during a dramatic transcriptional reprogramming—the response to diamide stress. We extend prior studies showing that steady-state histone modification patterns reflect genomic processes, especially transcription, and display limited combinatorial complexity. Interestingly, during the stress response we document a modest increase in the combinatorial complexity of histone modification space, resulting from roughly 3% of all nucleosomes transiently populating rare histone modification states. Most of these rare histone states result from differences in the kinetics of histone modification that transiently uncouple highly correlated marks, with slow histone methylation changes often lagging behind the more rapid acetylation changes. Explicit analysis of modification dynamics uncovers ordered sequences of events in gene activation and repression. Together, our results provide a comprehensive view of chromatin dynamics during a massive transcriptional upheaval.
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spelling pubmed-44053552015-04-26 High-Resolution Chromatin Dynamics during a Yeast Stress Response Weiner, Assaf Hsieh, Tsung-Han S. Appleboim, Alon Chen, Hsiuyi V. Rahat, Ayelet Amit, Ido Rando, Oliver J. Friedman, Nir Mol Cell Resource Covalent histone modifications are highly conserved and play multiple roles in eukaryotic transcription regulation. Here, we mapped 26 histone modifications genome-wide in exponentially growing yeast and during a dramatic transcriptional reprogramming—the response to diamide stress. We extend prior studies showing that steady-state histone modification patterns reflect genomic processes, especially transcription, and display limited combinatorial complexity. Interestingly, during the stress response we document a modest increase in the combinatorial complexity of histone modification space, resulting from roughly 3% of all nucleosomes transiently populating rare histone modification states. Most of these rare histone states result from differences in the kinetics of histone modification that transiently uncouple highly correlated marks, with slow histone methylation changes often lagging behind the more rapid acetylation changes. Explicit analysis of modification dynamics uncovers ordered sequences of events in gene activation and repression. Together, our results provide a comprehensive view of chromatin dynamics during a massive transcriptional upheaval. Cell Press 2015-04-16 /pmc/articles/PMC4405355/ /pubmed/25801168 http://dx.doi.org/10.1016/j.molcel.2015.02.002 Text en © 2015 The Authors 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 Resource
Weiner, Assaf
Hsieh, Tsung-Han S.
Appleboim, Alon
Chen, Hsiuyi V.
Rahat, Ayelet
Amit, Ido
Rando, Oliver J.
Friedman, Nir
High-Resolution Chromatin Dynamics during a Yeast Stress Response
title High-Resolution Chromatin Dynamics during a Yeast Stress Response
title_full High-Resolution Chromatin Dynamics during a Yeast Stress Response
title_fullStr High-Resolution Chromatin Dynamics during a Yeast Stress Response
title_full_unstemmed High-Resolution Chromatin Dynamics during a Yeast Stress Response
title_short High-Resolution Chromatin Dynamics during a Yeast Stress Response
title_sort high-resolution chromatin dynamics during a yeast stress response
topic Resource
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4405355/
https://www.ncbi.nlm.nih.gov/pubmed/25801168
http://dx.doi.org/10.1016/j.molcel.2015.02.002
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