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Chromatin topology is coupled to Polycomb group protein subnuclear organization

Author

Listed:
  • Ajazul H. Wani

    (Massachusetts General Hospital
    Harvard Medical School
    Present address: Department of Biotechnology, University of Kashmir, Srinagar, Jammu and Kashmir , India)

  • Alistair N. Boettiger

    (Howard Hughes Medical Institute, Harvard University Cambridge
    Harvard University
    Harvard University)

  • Patrick Schorderet

    (Massachusetts General Hospital
    Harvard Medical School)

  • Ayla Ergun

    (Massachusetts General Hospital)

  • Christine Münger

    (Institut de recherches cliniques de Montréal
    Present address: IniXium Inc., Laval, Quebec, Canada H7V 5B7)

  • Ruslan I. Sadreyev

    (Massachusetts General Hospital
    Massachusetts General Hospital and Harvard Medical School)

  • Xiaowei Zhuang

    (Howard Hughes Medical Institute, Harvard University Cambridge
    Harvard University
    Harvard University)

  • Robert E. Kingston

    (Massachusetts General Hospital
    Harvard Medical School)

  • Nicole J. Francis

    (Institut de recherches cliniques de Montréal
    Université de Montréal)

Abstract

The genomes of metazoa are organized at multiple scales. Many proteins that regulate genome architecture, including Polycomb group (PcG) proteins, form subnuclear structures. Deciphering mechanistic links between protein organization and chromatin architecture requires precise description and mechanistic perturbations of both. Using super-resolution microscopy, here we show that PcG proteins are organized into hundreds of nanoscale protein clusters. We manipulated PcG clusters by disrupting the polymerization activity of the sterile alpha motif (SAM) of the PcG protein Polyhomeotic (Ph) or by increasing Ph levels. Ph with mutant SAM disrupts clustering of endogenous PcG complexes and chromatin interactions while elevating Ph level increases cluster number and chromatin interactions. These effects can be captured by molecular simulations based on a previously described chromatin polymer model. Both perturbations also alter gene expression. Organization of PcG proteins into small, abundant clusters on chromatin through Ph SAM polymerization activity may shape genome architecture through chromatin interactions.

Suggested Citation

  • Ajazul H. Wani & Alistair N. Boettiger & Patrick Schorderet & Ayla Ergun & Christine Münger & Ruslan I. Sadreyev & Xiaowei Zhuang & Robert E. Kingston & Nicole J. Francis, 2016. "Chromatin topology is coupled to Polycomb group protein subnuclear organization," Nature Communications, Nature, vol. 7(1), pages 1-13, April.
  • Handle: RePEc:nat:natcom:v:7:y:2016:i:1:d:10.1038_ncomms10291
    DOI: 10.1038/ncomms10291
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    Cited by:

    1. Surya K Ghosh & Daniel Jost, 2018. "How epigenome drives chromatin folding and dynamics, insights from efficient coarse-grained models of chromosomes," PLOS Computational Biology, Public Library of Science, vol. 14(5), pages 1-26, May.
    2. Marieke R. Wensveen & Aditya A. Dixit & Robin Schendel & Apfrida Kendek & Jan-Paul Lambooij & Marcel Tijsterman & Serafin U. Colmenares & Aniek Janssen, 2024. "Double-strand breaks in facultative heterochromatin require specific movements and chromatin changes for efficient repair," Nature Communications, Nature, vol. 15(1), pages 1-14, December.
    3. 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.

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