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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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    References listed on IDEAS

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