Effective dynamics of nucleosome configurations at the yeast PHO5 promoter
Chromatin dynamics are mediated by remodeling enzymes and play crucial roles in gene regulation, as established in a paradigmatic model, the Saccharomyces cerevisiae PHO5 promoter. However, effective nucleosome dynamics, that is, trajectories of promoter nucleosome configurations, remain elusive. He...
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doaj-f240a2671c0441f4a79cba55a39997bb2021-05-05T22:51:53ZengeLife Sciences Publications LtdeLife2050-084X2021-03-011010.7554/eLife.58394Effective dynamics of nucleosome configurations at the yeast PHO5 promoterMichael Roland Wolff0https://orcid.org/0000-0002-4677-4023Andrea Schmid1Philipp Korber2https://orcid.org/0000-0001-7526-6549Ulrich Gerland3https://orcid.org/0000-0002-0859-6422Department of Physics, Technical University of Munich, Garching, GermanyMolecular Biology Division, Biomedical Center, Faculty of Medicine, Ludwig-Maximilians-Universität München, Planegg-Martinsried, GermanyMolecular Biology Division, Biomedical Center, Faculty of Medicine, Ludwig-Maximilians-Universität München, Planegg-Martinsried, GermanyDepartment of Physics, Technical University of Munich, Garching, GermanyChromatin dynamics are mediated by remodeling enzymes and play crucial roles in gene regulation, as established in a paradigmatic model, the Saccharomyces cerevisiae PHO5 promoter. However, effective nucleosome dynamics, that is, trajectories of promoter nucleosome configurations, remain elusive. Here, we infer such dynamics from the integration of published single-molecule data capturing multi-nucleosome configurations for repressed to fully active PHO5 promoter states with other existing histone turnover and new chromatin accessibility data. We devised and systematically investigated a new class of ‘regulated on-off-slide’ models simulating global and local nucleosome (dis)assembly and sliding. Only seven of 68,145 models agreed well with all data. All seven models involve sliding and the known central role of the N-2 nucleosome, but regulate promoter state transitions by modulating just one assembly rather than disassembly process. This is consistent with but challenges common interpretations of previous observations at the PHO5 promoter and suggests chromatin opening by binding competition.https://elifesciences.org/articles/58394PHO5 promoternucleosome dynamicsnucleosome configurationschromatin regulationchromatin remodeling |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Michael Roland Wolff Andrea Schmid Philipp Korber Ulrich Gerland |
spellingShingle |
Michael Roland Wolff Andrea Schmid Philipp Korber Ulrich Gerland Effective dynamics of nucleosome configurations at the yeast PHO5 promoter eLife PHO5 promoter nucleosome dynamics nucleosome configurations chromatin regulation chromatin remodeling |
author_facet |
Michael Roland Wolff Andrea Schmid Philipp Korber Ulrich Gerland |
author_sort |
Michael Roland Wolff |
title |
Effective dynamics of nucleosome configurations at the yeast PHO5 promoter |
title_short |
Effective dynamics of nucleosome configurations at the yeast PHO5 promoter |
title_full |
Effective dynamics of nucleosome configurations at the yeast PHO5 promoter |
title_fullStr |
Effective dynamics of nucleosome configurations at the yeast PHO5 promoter |
title_full_unstemmed |
Effective dynamics of nucleosome configurations at the yeast PHO5 promoter |
title_sort |
effective dynamics of nucleosome configurations at the yeast pho5 promoter |
publisher |
eLife Sciences Publications Ltd |
series |
eLife |
issn |
2050-084X |
publishDate |
2021-03-01 |
description |
Chromatin dynamics are mediated by remodeling enzymes and play crucial roles in gene regulation, as established in a paradigmatic model, the Saccharomyces cerevisiae PHO5 promoter. However, effective nucleosome dynamics, that is, trajectories of promoter nucleosome configurations, remain elusive. Here, we infer such dynamics from the integration of published single-molecule data capturing multi-nucleosome configurations for repressed to fully active PHO5 promoter states with other existing histone turnover and new chromatin accessibility data. We devised and systematically investigated a new class of ‘regulated on-off-slide’ models simulating global and local nucleosome (dis)assembly and sliding. Only seven of 68,145 models agreed well with all data. All seven models involve sliding and the known central role of the N-2 nucleosome, but regulate promoter state transitions by modulating just one assembly rather than disassembly process. This is consistent with but challenges common interpretations of previous observations at the PHO5 promoter and suggests chromatin opening by binding competition. |
topic |
PHO5 promoter nucleosome dynamics nucleosome configurations chromatin regulation chromatin remodeling |
url |
https://elifesciences.org/articles/58394 |
work_keys_str_mv |
AT michaelrolandwolff effectivedynamicsofnucleosomeconfigurationsattheyeastpho5promoter AT andreaschmid effectivedynamicsofnucleosomeconfigurationsattheyeastpho5promoter AT philippkorber effectivedynamicsofnucleosomeconfigurationsattheyeastpho5promoter AT ulrichgerland effectivedynamicsofnucleosomeconfigurationsattheyeastpho5promoter |
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1721457579580719104 |