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Linker histone H1 and H3K56 acetylation are antagonistic regulators of nucleosome dynamics

H1 linker histones are highly abundant proteins that compact nucleosomes and chromatin to regulate DNA accessibility and transcription. However, the mechanisms that target H1 regulation to specific regions of eukaryotic genomes are unknown. Here we report fluorescence measurements of human H1 regula...

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Autores principales: Bernier, Morgan, Luo, Yi, Nwokelo, Kingsley C., Goodwin, Michelle, Dreher, Sarah J., Zhang, Pei, Parthun, Mark R., Fondufe-Mittendorf, Yvonne, Ottesen, Jennifer J., Poirier, Michael G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4682114/
https://www.ncbi.nlm.nih.gov/pubmed/26648124
http://dx.doi.org/10.1038/ncomms10152
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author Bernier, Morgan
Luo, Yi
Nwokelo, Kingsley C.
Goodwin, Michelle
Dreher, Sarah J.
Zhang, Pei
Parthun, Mark R.
Fondufe-Mittendorf, Yvonne
Ottesen, Jennifer J.
Poirier, Michael G.
author_facet Bernier, Morgan
Luo, Yi
Nwokelo, Kingsley C.
Goodwin, Michelle
Dreher, Sarah J.
Zhang, Pei
Parthun, Mark R.
Fondufe-Mittendorf, Yvonne
Ottesen, Jennifer J.
Poirier, Michael G.
author_sort Bernier, Morgan
collection PubMed
description H1 linker histones are highly abundant proteins that compact nucleosomes and chromatin to regulate DNA accessibility and transcription. However, the mechanisms that target H1 regulation to specific regions of eukaryotic genomes are unknown. Here we report fluorescence measurements of human H1 regulation of nucleosome dynamics and transcription factor (TF) binding within nucleosomes. H1 does not block TF binding, instead it suppresses nucleosome unwrapping to reduce DNA accessibility within H1-bound nucleosomes. We then investigated H1 regulation by H3K56 and H3K122 acetylation, two transcriptional activating histone post translational modifications (PTMs). Only H3K56 acetylation, which increases nucleosome unwrapping, abolishes H1.0 reduction of TF binding. These findings show that nucleosomes remain dynamic, while H1 is bound and H1 dissociation is not required for TF binding within the nucleosome. Furthermore, our H3K56 acetylation measurements suggest that a single-histone PTM can define regions of the genome that are not regulated by H1.
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spelling pubmed-46821142015-12-29 Linker histone H1 and H3K56 acetylation are antagonistic regulators of nucleosome dynamics Bernier, Morgan Luo, Yi Nwokelo, Kingsley C. Goodwin, Michelle Dreher, Sarah J. Zhang, Pei Parthun, Mark R. Fondufe-Mittendorf, Yvonne Ottesen, Jennifer J. Poirier, Michael G. Nat Commun Article H1 linker histones are highly abundant proteins that compact nucleosomes and chromatin to regulate DNA accessibility and transcription. However, the mechanisms that target H1 regulation to specific regions of eukaryotic genomes are unknown. Here we report fluorescence measurements of human H1 regulation of nucleosome dynamics and transcription factor (TF) binding within nucleosomes. H1 does not block TF binding, instead it suppresses nucleosome unwrapping to reduce DNA accessibility within H1-bound nucleosomes. We then investigated H1 regulation by H3K56 and H3K122 acetylation, two transcriptional activating histone post translational modifications (PTMs). Only H3K56 acetylation, which increases nucleosome unwrapping, abolishes H1.0 reduction of TF binding. These findings show that nucleosomes remain dynamic, while H1 is bound and H1 dissociation is not required for TF binding within the nucleosome. Furthermore, our H3K56 acetylation measurements suggest that a single-histone PTM can define regions of the genome that are not regulated by H1. Nature Publishing Group 2015-12-09 /pmc/articles/PMC4682114/ /pubmed/26648124 http://dx.doi.org/10.1038/ncomms10152 Text en Copyright © 2015, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Bernier, Morgan
Luo, Yi
Nwokelo, Kingsley C.
Goodwin, Michelle
Dreher, Sarah J.
Zhang, Pei
Parthun, Mark R.
Fondufe-Mittendorf, Yvonne
Ottesen, Jennifer J.
Poirier, Michael G.
Linker histone H1 and H3K56 acetylation are antagonistic regulators of nucleosome dynamics
title Linker histone H1 and H3K56 acetylation are antagonistic regulators of nucleosome dynamics
title_full Linker histone H1 and H3K56 acetylation are antagonistic regulators of nucleosome dynamics
title_fullStr Linker histone H1 and H3K56 acetylation are antagonistic regulators of nucleosome dynamics
title_full_unstemmed Linker histone H1 and H3K56 acetylation are antagonistic regulators of nucleosome dynamics
title_short Linker histone H1 and H3K56 acetylation are antagonistic regulators of nucleosome dynamics
title_sort linker histone h1 and h3k56 acetylation are antagonistic regulators of nucleosome dynamics
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4682114/
https://www.ncbi.nlm.nih.gov/pubmed/26648124
http://dx.doi.org/10.1038/ncomms10152
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