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Loss of cohesin regulator PDS5A reveals repressive role of Polycomb loops

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  • Daniel Bsteh

    (Vienna BioCenter (VBC)
    Doctoral School of the University of Vienna and Medical University of Vienna
    University of Southern California
    University of Southern California)

  • Hagar F. Moussa

    (Vienna BioCenter (VBC)
    Doctoral School of the University of Vienna and Medical University of Vienna
    Boston University)

  • Georg Michlits

    (Vienna BioCenter (VBC)
    Doctoral School of the University of Vienna and Medical University of Vienna
    JLP Health GmbH)

  • Ramesh Yelagandula

    (Vienna BioCenter (VBC)
    Centre for DNA Fingerprinting and Diagnostics (CDFD), Uppal)

  • Jingkui Wang

    (Vienna BioCenter (VBC)
    Research Institute of Molecular Pathology (IMP), Vienna BioCenter (VBC))

  • Ulrich Elling

    (Vienna BioCenter (VBC))

  • Oliver Bell

    (Vienna BioCenter (VBC)
    University of Southern California)

Abstract

Polycomb Repressive Complexes 1 and 2 (PRC1, PRC2) are conserved epigenetic regulators that promote transcriptional gene silencing. PRC1 and PRC2 converge on shared targets, catalyzing repressive histone modifications. Additionally, a subset of PRC1/PRC2 targets engage in long-range interactions whose functions in gene silencing are poorly understood. Using a CRISPR screen in mouse embryonic stem cells, we found that the cohesin regulator PDS5A links transcriptional silencing by Polycomb and 3D genome organization. PDS5A deletion impairs cohesin unloading and results in derepression of a subset of endogenous PRC1/PRC2 target genes. Importantly, derepression is not linked to loss of Polycomb chromatin domains. Instead, PDS5A removal causes aberrant cohesin activity leading to ectopic insulation sites, which disrupt the formation of ultra-long Polycomb loops. We show that these loops are important for robust silencing at a subset of PRC1/PRC2 target genes and that maintenance of cohesin-dependent genome architecture is critical for Polycomb regulation.

Suggested Citation

  • Daniel Bsteh & Hagar F. Moussa & Georg Michlits & Ramesh Yelagandula & Jingkui Wang & Ulrich Elling & Oliver Bell, 2023. "Loss of cohesin regulator PDS5A reveals repressive role of Polycomb loops," Nature Communications, Nature, vol. 14(1), pages 1-16, December.
  • Handle: RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-43869-w
    DOI: 10.1038/s41467-023-43869-w
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    References listed on IDEAS

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    1. Georg A. Busslinger & Roman R. Stocsits & Petra van der Lelij & Elin Axelsson & Antonio Tedeschi & Niels Galjart & Jan-Michael Peters, 2017. "Cohesin is positioned in mammalian genomes by transcription, CTCF and Wapl," Nature, Nature, vol. 544(7651), pages 503-507, April.
    2. Hengbin Wang & Liangjun Wang & Hediye Erdjument-Bromage & Miguel Vidal & Paul Tempst & Richard S. Jones & Yi Zhang, 2004. "Role of histone H2A ubiquitination in Polycomb silencing," Nature, Nature, vol. 431(7010), pages 873-878, October.
    3. Ho Lam Chan & Felipe Beckedorff & Yusheng Zhang & Jenaro Garcia-Huidobro & Hua Jiang & Antonio Colaprico & Daniel Bilbao & Maria E. Figueroa & John LaCava & Ramin Shiekhattar & Lluis Morey, 2018. "Polycomb complexes associate with enhancers and promote oncogenic transcriptional programs in cancer through multiple mechanisms," Nature Communications, Nature, vol. 9(1), pages 1-16, December.
    4. Haojie Li & Robert Liefke & Junyi Jiang & Jesse Vigoda Kurland & Wei Tian & Pujuan Deng & Weidi Zhang & Qian He & Dinshaw J. Patel & Martha L. Bulyk & Yang Shi & Zhanxin Wang, 2017. "Polycomb-like proteins link the PRC2 complex to CpG islands," Nature, Nature, vol. 549(7671), pages 287-291, September.
    5. Antonio Tedeschi & Gordana Wutz & Sébastien Huet & Markus Jaritz & Annelie Wuensche & Erika Schirghuber & Iain Finley Davidson & Wen Tang & David A. Cisneros & Venugopal Bhaskara & Tomoko Nishiyama & , 2013. "Wapl is an essential regulator of chromatin structure and chromosome segregation," Nature, Nature, vol. 501(7468), pages 564-568, September.
    6. Christian H. Haering & Ana-Maria Farcas & Prakash Arumugam & Jean Metson & Kim Nasmyth, 2008. "The cohesin ring concatenates sister DNA molecules," Nature, Nature, vol. 454(7202), pages 297-301, July.
    7. Michael H. Kagey & Jamie J. Newman & Steve Bilodeau & Ye Zhan & David A. Orlando & Nynke L. van Berkum & Christopher C. Ebmeier & Jesse Goossens & Peter B. Rahl & Stuart S. Levine & Dylan J. Taatjes &, 2010. "Mediator and cohesin connect gene expression and chromatin architecture," Nature, Nature, vol. 467(7314), pages 430-435, September.
    8. Yuko Katoh-Fukui & Reiko Tsuchiya & Toshihiko Shiroishi & Yoko Nakahara & Naoko Hashimoto & Kousei Noguchi & Toru Higashinakagawa, 1998. "Male-to-female sex reversal in M33 mutant mice," Nature, Nature, vol. 393(6686), pages 688-692, June.
    9. Emily Crane & Qian Bian & Rachel Patton McCord & Bryan R. Lajoie & Bayly S. Wheeler & Edward J. Ralston & Satoru Uzawa & Job Dekker & Barbara J. Meyer, 2015. "Condensin-driven remodelling of X chromosome topology during dosage compensation," Nature, Nature, vol. 523(7559), pages 240-244, July.
    10. Ulrich Elling & Reiner A. Wimmer & Andreas Leibbrandt & Thomas Burkard & Georg Michlits & Alexandra Leopoldi & Thomas Micheler & Dana Abdeen & Sergei Zhuk & Irene M. Aspalter & Cornelia Handl & Julia , 2017. "A reversible haploid mouse embryonic stem cell biobank resource for functional genomics," Nature, Nature, vol. 550(7674), pages 114-118, October.
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