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Polycomb condensates can promote epigenetic marks but are not required for sustained chromatin compaction

Organization of the genome into transcriptionally active euchromatin and silenced heterochromatin is essential for eukaryotic cell function. Phase-separation has been implicated in heterochromatin formation, but it is unclear how phase-separated condensates can contribute to stable repression, parti...

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Autores principales: Eeftens, Jorine M., Kapoor, Manya, Michieletto, Davide, Brangwynne, Clifford P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8497513/
https://www.ncbi.nlm.nih.gov/pubmed/34620850
http://dx.doi.org/10.1038/s41467-021-26147-5
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author Eeftens, Jorine M.
Kapoor, Manya
Michieletto, Davide
Brangwynne, Clifford P.
author_facet Eeftens, Jorine M.
Kapoor, Manya
Michieletto, Davide
Brangwynne, Clifford P.
author_sort Eeftens, Jorine M.
collection PubMed
description Organization of the genome into transcriptionally active euchromatin and silenced heterochromatin is essential for eukaryotic cell function. Phase-separation has been implicated in heterochromatin formation, but it is unclear how phase-separated condensates can contribute to stable repression, particularly for heritable epigenetic changes. Polycomb complex PRC1 is key for heterochromatin formation, but the multitude of Polycomb proteins has hindered our understanding of their collective contribution to chromatin repression. Here, we show that PRC1 forms multicomponent condensates through hetero-oligomerization. They preferentially seed at H3K27me3 marks, and subsequently write H2AK119Ub marks. We show that inducing Polycomb phase-separation can cause chromatin compaction, but polycomb condensates are dispensable for maintenance of the compacted state. Our data and simulations are consistent with a model in which the time integral of Polycomb phase-separation is progressively recorded in repressive histone marks, which subsequently drive compaction. These findings link the equilibrium thermodynamics of phase-separation with the fundamentally non-equilibrium concept of epigenetic memory.
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spelling pubmed-84975132021-10-22 Polycomb condensates can promote epigenetic marks but are not required for sustained chromatin compaction Eeftens, Jorine M. Kapoor, Manya Michieletto, Davide Brangwynne, Clifford P. Nat Commun Article Organization of the genome into transcriptionally active euchromatin and silenced heterochromatin is essential for eukaryotic cell function. Phase-separation has been implicated in heterochromatin formation, but it is unclear how phase-separated condensates can contribute to stable repression, particularly for heritable epigenetic changes. Polycomb complex PRC1 is key for heterochromatin formation, but the multitude of Polycomb proteins has hindered our understanding of their collective contribution to chromatin repression. Here, we show that PRC1 forms multicomponent condensates through hetero-oligomerization. They preferentially seed at H3K27me3 marks, and subsequently write H2AK119Ub marks. We show that inducing Polycomb phase-separation can cause chromatin compaction, but polycomb condensates are dispensable for maintenance of the compacted state. Our data and simulations are consistent with a model in which the time integral of Polycomb phase-separation is progressively recorded in repressive histone marks, which subsequently drive compaction. These findings link the equilibrium thermodynamics of phase-separation with the fundamentally non-equilibrium concept of epigenetic memory. Nature Publishing Group UK 2021-10-07 /pmc/articles/PMC8497513/ /pubmed/34620850 http://dx.doi.org/10.1038/s41467-021-26147-5 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Eeftens, Jorine M.
Kapoor, Manya
Michieletto, Davide
Brangwynne, Clifford P.
Polycomb condensates can promote epigenetic marks but are not required for sustained chromatin compaction
title Polycomb condensates can promote epigenetic marks but are not required for sustained chromatin compaction
title_full Polycomb condensates can promote epigenetic marks but are not required for sustained chromatin compaction
title_fullStr Polycomb condensates can promote epigenetic marks but are not required for sustained chromatin compaction
title_full_unstemmed Polycomb condensates can promote epigenetic marks but are not required for sustained chromatin compaction
title_short Polycomb condensates can promote epigenetic marks but are not required for sustained chromatin compaction
title_sort polycomb condensates can promote epigenetic marks but are not required for sustained chromatin compaction
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8497513/
https://www.ncbi.nlm.nih.gov/pubmed/34620850
http://dx.doi.org/10.1038/s41467-021-26147-5
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