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Histone H2A variants confer specific properties to nucleosomes and impact on chromatin accessibility
In eukaryotes, variants of core histone H2A are selectively incorporated in distinct functional domains of chromatin and are distinguished by conserved sequences of their C-terminal tail, the L1 loop and the docking domain, suggesting that each variant confers specific properties to the nucleosome....
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6125630/ https://www.ncbi.nlm.nih.gov/pubmed/29945241 http://dx.doi.org/10.1093/nar/gky540 |
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author | Osakabe, Akihisa Lorković, Zdravko J Kobayashi, Wataru Tachiwana, Hiroaki Yelagandula, Ramesh Kurumizaka, Hitoshi Berger, Frédéric |
author_facet | Osakabe, Akihisa Lorković, Zdravko J Kobayashi, Wataru Tachiwana, Hiroaki Yelagandula, Ramesh Kurumizaka, Hitoshi Berger, Frédéric |
author_sort | Osakabe, Akihisa |
collection | PubMed |
description | In eukaryotes, variants of core histone H2A are selectively incorporated in distinct functional domains of chromatin and are distinguished by conserved sequences of their C-terminal tail, the L1 loop and the docking domain, suggesting that each variant confers specific properties to the nucleosome. Chromatin of flowering plants contains four types of H2A variants, which biochemical properties have not been characterized. We report that in contrast with animals, in Arabidopsis thaliana H2A variants define only four major types of homotypic nucleosomes containing exclusively H2A, H2A.Z, H2A.X or H2A.W. In vitro assays show that the L1 loop and the docking domain confer distinct stability of the nucleosome. In vivo and in vitro assays suggest that the L1 loop and the docking domain cooperate with the C-terminal tail to regulate chromatin accessibility. Based on these findings we conclude that the type of H2A variant in the nucleosome impacts on its interaction with DNA and propose that H2A variants regulate the dynamics of chromatin accessibility. In plants, the predominance of homotypic nucleosomes with specific physical properties and their specific localization to distinct domains suggest that H2A variants play a dominant role in chromatin dynamics and function. |
format | Online Article Text |
id | pubmed-6125630 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-61256302018-09-11 Histone H2A variants confer specific properties to nucleosomes and impact on chromatin accessibility Osakabe, Akihisa Lorković, Zdravko J Kobayashi, Wataru Tachiwana, Hiroaki Yelagandula, Ramesh Kurumizaka, Hitoshi Berger, Frédéric Nucleic Acids Res Gene regulation, Chromatin and Epigenetics In eukaryotes, variants of core histone H2A are selectively incorporated in distinct functional domains of chromatin and are distinguished by conserved sequences of their C-terminal tail, the L1 loop and the docking domain, suggesting that each variant confers specific properties to the nucleosome. Chromatin of flowering plants contains four types of H2A variants, which biochemical properties have not been characterized. We report that in contrast with animals, in Arabidopsis thaliana H2A variants define only four major types of homotypic nucleosomes containing exclusively H2A, H2A.Z, H2A.X or H2A.W. In vitro assays show that the L1 loop and the docking domain confer distinct stability of the nucleosome. In vivo and in vitro assays suggest that the L1 loop and the docking domain cooperate with the C-terminal tail to regulate chromatin accessibility. Based on these findings we conclude that the type of H2A variant in the nucleosome impacts on its interaction with DNA and propose that H2A variants regulate the dynamics of chromatin accessibility. In plants, the predominance of homotypic nucleosomes with specific physical properties and their specific localization to distinct domains suggest that H2A variants play a dominant role in chromatin dynamics and function. Oxford University Press 2018-09-06 2018-06-26 /pmc/articles/PMC6125630/ /pubmed/29945241 http://dx.doi.org/10.1093/nar/gky540 Text en © The Author(s) 2018. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Gene regulation, Chromatin and Epigenetics Osakabe, Akihisa Lorković, Zdravko J Kobayashi, Wataru Tachiwana, Hiroaki Yelagandula, Ramesh Kurumizaka, Hitoshi Berger, Frédéric Histone H2A variants confer specific properties to nucleosomes and impact on chromatin accessibility |
title | Histone H2A variants confer specific properties to nucleosomes and impact on chromatin accessibility |
title_full | Histone H2A variants confer specific properties to nucleosomes and impact on chromatin accessibility |
title_fullStr | Histone H2A variants confer specific properties to nucleosomes and impact on chromatin accessibility |
title_full_unstemmed | Histone H2A variants confer specific properties to nucleosomes and impact on chromatin accessibility |
title_short | Histone H2A variants confer specific properties to nucleosomes and impact on chromatin accessibility |
title_sort | histone h2a variants confer specific properties to nucleosomes and impact on chromatin accessibility |
topic | Gene regulation, Chromatin and Epigenetics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6125630/ https://www.ncbi.nlm.nih.gov/pubmed/29945241 http://dx.doi.org/10.1093/nar/gky540 |
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