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The 3D enhancer network of the developing T cell genome is shaped by SATB1

Author

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  • Tomas Zelenka

    (University of Crete
    Institute of Molecular Biology and Biotechnology—Foundation for Research and Technology Hellas
    H. Lee Moffitt Cancer Center and Research Institute)

  • Antonios Klonizakis

    (University of Crete)

  • Despina Tsoukatou

    (Institute of Molecular Biology and Biotechnology—Foundation for Research and Technology Hellas)

  • Dionysios-Alexandros Papamatheakis

    (University of Crete
    Institute of Molecular Biology and Biotechnology—Foundation for Research and Technology Hellas)

  • Sören Franzenburg

    (University Hospital Schleswig Holstein)

  • Petros Tzerpos

    (University of Crete
    University of Debrecen)

  • Ioannis-Rafail Tzonevrakis

    (University of Crete)

  • George Papadogkonas

    (University of Crete
    Institute of Molecular Biology and Biotechnology—Foundation for Research and Technology Hellas)

  • Manouela Kapsetaki

    (Institute of Molecular Biology and Biotechnology—Foundation for Research and Technology Hellas)

  • Christoforos Nikolaou

    (University of Crete
    Institute of Molecular Biology and Biotechnology—Foundation for Research and Technology Hellas
    Biomedical Sciences Research Centre “Alexander Fleming”)

  • Dariusz Plewczynski

    (Warsaw University of Technology
    University of Warsaw)

  • Charalampos Spilianakis

    (University of Crete
    Institute of Molecular Biology and Biotechnology—Foundation for Research and Technology Hellas)

Abstract

Mechanisms of tissue-specific gene expression regulation via 3D genome organization are poorly understood. Here we uncover the regulatory chromatin network of developing T cells and identify SATB1, a tissue-specific genome organizer, enriched at the anchors of promoter-enhancer loops. We have generated a T-cell specific Satb1 conditional knockout mouse which allows us to infer the molecular mechanisms responsible for the deregulation of its immune system. H3K27ac HiChIP and Hi-C experiments indicate that SATB1-dependent promoter-enhancer loops regulate expression of master regulator genes (such as Bcl6), the T cell receptor locus and adhesion molecule genes, collectively being critical for cell lineage specification and immune system homeostasis. SATB1-dependent regulatory chromatin loops represent a more refined layer of genome organization built upon a high-order scaffold provided by CTCF and other factors. Overall, our findings unravel the function of a tissue-specific factor that controls transcription programs, via spatial chromatin arrangements complementary to the chromatin structure imposed by ubiquitously expressed genome organizers.

Suggested Citation

  • Tomas Zelenka & Antonios Klonizakis & Despina Tsoukatou & Dionysios-Alexandros Papamatheakis & Sören Franzenburg & Petros Tzerpos & Ioannis-Rafail Tzonevrakis & George Papadogkonas & Manouela Kapsetak, 2022. "The 3D enhancer network of the developing T cell genome is shaped by SATB1," Nature Communications, Nature, vol. 13(1), pages 1-22, December.
  • Handle: RePEc:nat:natcom:v:13:y:2022:i:1:d:10.1038_s41467-022-34345-y
    DOI: 10.1038/s41467-022-34345-y
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    as
    1. Alexander Favorov & Loris Mularoni & Leslie M Cope & Yulia Medvedeva & Andrey A Mironov & Vsevolod J Makeev & Sarah J Wheelan, 2012. "Exploring Massive, Genome Scale Datasets with the GenometriCorr Package," PLOS Computational Biology, Public Library of Science, vol. 8(5), pages 1-12, May.
    2. Jesse R. Dixon & Siddarth Selvaraj & Feng Yue & Audrey Kim & Yan Li & Yin Shen & Ming Hu & Jun S. Liu & Bing Ren, 2012. "Topological domains in mammalian genomes identified by analysis of chromatin interactions," Nature, Nature, vol. 485(7398), pages 376-380, May.
    3. Keiko Yasuda & Yohko Kitagawa & Ryoji Kawakami & Yoshitaka Isaka & Hitomi Watanabe & Gen Kondoh & Terumi Kohwi-Shigematsu & Shimon Sakaguchi & Keiji Hirota, 2019. "Satb1 regulates the effector program of encephalitogenic tissue Th17 cells in chronic inflammation," Nature Communications, Nature, vol. 10(1), pages 1-14, December.
    4. Ralph Stadhouders & Guillaume J. Filion & Thomas Graf, 2019. "Transcription factors and 3D genome conformation in cell-fate decisions," Nature, Nature, vol. 569(7756), pages 345-354, May.
    5. Vlad C. Seitan & Bingtao Hao & Kikuë Tachibana-Konwalski & Thais Lavagnolli & Hegias Mira-Bontenbal & Karen E. Brown & Grace Teng & Tom Carroll & Anna Terry & Katie Horan & Hendrik Marks & David J. Ad, 2011. "A role for cohesin in T-cell-receptor rearrangement and thymocyte differentiation," Nature, Nature, vol. 476(7361), pages 467-471, August.
    6. Yin Shen & Feng Yue & David F. McCleary & Zhen Ye & Lee Edsall & Samantha Kuan & Ulrich Wagner & Jesse Dixon & Leonard Lee & Victor V. Lobanenkov & Bing Ren, 2012. "A map of the cis-regulatory sequences in the mouse genome," Nature, Nature, vol. 488(7409), pages 116-120, August.
    7. Wibke Schwarzer & Nezar Abdennur & Anton Goloborodko & Aleksandra Pekowska & Geoffrey Fudenberg & Yann Loe-Mie & Nuno A Fonseca & Wolfgang Huber & Christian H. Haering & Leonid Mirny & Francois Spitz, 2017. "Two independent modes of chromatin organization revealed by cohesin removal," Nature, Nature, vol. 551(7678), pages 51-56, November.
    8. Elphège P. Nora & Bryan R. Lajoie & Edda G. Schulz & Luca Giorgetti & Ikuhiro Okamoto & Nicolas Servant & Tristan Piolot & Nynke L. van Berkum & Johannes Meisig & John Sedat & Joost Gribnau & Emmanuel, 2012. "Spatial partitioning of the regulatory landscape of the X-inactivation centre," Nature, Nature, vol. 485(7398), pages 381-385, May.
    9. Nicholas T. Crump & Erica Ballabio & Laura Godfrey & Ross Thorne & Emmanouela Repapi & Jon Kerry & Marta Tapia & Peng Hua & Christoffer Lagerholm & Panagis Filippakopoulos & James O. J. Davies & Thoma, 2021. "BET inhibition disrupts transcription but retains enhancer-promoter contact," Nature Communications, Nature, vol. 12(1), pages 1-15, December.
    10. Hye-Jung Han & Jose Russo & Yoshinori Kohwi & Terumi Kohwi-Shigematsu, 2008. "SATB1 reprogrammes gene expression to promote breast tumour growth and metastasis," Nature, Nature, vol. 452(7184), pages 187-193, March.
    11. Charalampos G. Spilianakis & Maria D. Lalioti & Terrence Town & Gap Ryol Lee & Richard A. Flavell, 2005. "Interchromosomal associations between alternatively expressed loci," Nature, Nature, vol. 435(7042), pages 637-645, June.
    12. Rajarshi P. Ghosh & Quanming Shi & Linfeng Yang & Michael P. Reddick & Tatiana Nikitina & Victor B. Zhurkin & Polly Fordyce & Timothy J. Stasevich & Howard Y. Chang & William J. Greenleaf & Jan T. Lip, 2019. "Satb1 integrates DNA binding site geometry and torsional stress to differentially target nucleosome-dense regions," Nature Communications, Nature, vol. 10(1), pages 1-16, December.
    Full references (including those not matched with items on IDEAS)

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