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

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  • Jorine M. Eeftens

    (Princeton University)

  • Manya Kapoor

    (Princeton University)

  • Davide Michieletto

    (University of Edinburgh
    University of Edinburgh)

  • Clifford P. Brangwynne

    (Princeton University
    The Howard Hughes Medical Institute)

Abstract

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.

Suggested Citation

  • Jorine M. Eeftens & Manya Kapoor & Davide Michieletto & Clifford P. Brangwynne, 2021. "Polycomb condensates can promote epigenetic marks but are not required for sustained chromatin compaction," Nature Communications, Nature, vol. 12(1), pages 1-12, December.
  • Handle: RePEc:nat:natcom:v:12:y:2021:i:1:d:10.1038_s41467-021-26147-5
    DOI: 10.1038/s41467-021-26147-5
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    Cited by:

    1. Wenqi Sun & Qianhua Dong & Xueqing Li & Jinxin Gao & Xianwen Ye & Chunyi Hu & Fei Li & Yong Chen, 2024. "The SUN-family protein Sad1 mediates heterochromatin spatial organization through interaction with histone H2A-H2B," Nature Communications, Nature, vol. 15(1), pages 1-13, December.
    2. Marios G. Koliopoulos & Reyhan Muhammad & Theodoros I. Roumeliotis & Fabienne Beuron & Jyoti S. Choudhary & Claudio Alfieri, 2022. "Structure of a nucleosome-bound MuvB transcription factor complex reveals DNA remodelling," Nature Communications, Nature, vol. 13(1), pages 1-14, December.
    3. Amanda Ames & Melissa Seman & Ajay Larkin & Gulzhan Raiymbek & Ziyuan Chen & Alex Levashkevich & Bokyung Kim & Julie Suzanne Biteen & Kaushik Ragunathan, 2024. "Epigenetic memory is governed by an effector recruitment specificity toggle in Heterochromatin Protein 1," Nature Communications, Nature, vol. 15(1), pages 1-17, December.

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