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A tissue-specific self-interacting chromatin domain forms independently of enhancer-promoter interactions

Author

Listed:
  • Jill M. Brown

    (MRC Weatherall Institute of Molecular Medicine, Oxford University)

  • Nigel A. Roberts

    (MRC Weatherall Institute of Molecular Medicine, Oxford University)

  • Bryony Graham

    (MRC Weatherall Institute of Molecular Medicine, Oxford University)

  • Dominic Waithe

    (MRC Weatherall Institute of Molecular Medicine)

  • Christoffer Lagerholm

    (MRC Weatherall Institute of Molecular Medicine)

  • Jelena M. Telenius

    (MRC Weatherall Institute of Molecular Medicine, Oxford University)

  • Sara Ornellas

    (MRC Weatherall Institute of Molecular Medicine, Oxford University)

  • A. Marieke Oudelaar

    (MRC Weatherall Institute of Molecular Medicine, Oxford University)

  • Caroline Scott

    (MRC Weatherall Institute of Molecular Medicine, Oxford University)

  • Izabela Szczerbal

    (MRC Weatherall Institute of Molecular Medicine, Oxford University
    Poznan University of Life Sciences)

  • Christian Babbs

    (MRC Weatherall Institute of Molecular Medicine, Oxford University)

  • Mira T. Kassouf

    (MRC Weatherall Institute of Molecular Medicine, Oxford University)

  • Jim R. Hughes

    (MRC Weatherall Institute of Molecular Medicine, Oxford University)

  • Douglas R. Higgs

    (MRC Weatherall Institute of Molecular Medicine, Oxford University)

  • Veronica J. Buckle

    (MRC Weatherall Institute of Molecular Medicine, Oxford University)

Abstract

Self-interacting chromatin domains encompass genes and their cis-regulatory elements; however, the three-dimensional form a domain takes, whether this relies on enhancer–promoter interactions, and the processes necessary to mediate the formation and maintenance of such domains, remain unclear. To examine these questions, here we use a combination of high-resolution chromosome conformation capture, a non-denaturing form of fluorescence in situ hybridisation and super-resolution imaging to study a 70 kb domain encompassing the mouse α-globin regulatory locus. We show that this region forms an erythroid-specific, decompacted, self-interacting domain, delimited by frequently apposed CTCF/cohesin binding sites early in terminal erythroid differentiation, and does not require transcriptional elongation for maintenance of the domain structure. Formation of this domain does not rely on interactions between the α-globin genes and their major enhancers, suggesting a transcription-independent mechanism for establishment of the domain. However, absence of the major enhancers does alter internal domain interactions. Formation of a loop domain therefore appears to be a mechanistic process that occurs irrespective of the specific interactions within.

Suggested Citation

  • Jill M. Brown & Nigel A. Roberts & Bryony Graham & Dominic Waithe & Christoffer Lagerholm & Jelena M. Telenius & Sara Ornellas & A. Marieke Oudelaar & Caroline Scott & Izabela Szczerbal & Christian Ba, 2018. "A tissue-specific self-interacting chromatin domain forms independently of enhancer-promoter interactions," Nature Communications, Nature, vol. 9(1), pages 1-15, December.
  • Handle: RePEc:nat:natcom:v:9:y:2018:i:1:d:10.1038_s41467-018-06248-4
    DOI: 10.1038/s41467-018-06248-4
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    Cited by:

    1. D. M. Jeziorska & E. A. J. Tunnacliffe & J. M. Brown & H. Ayyub & J. Sloane-Stanley & J. A. Sharpe & B. C. Lagerholm & C. Babbs & A. J. H. Smith & V. J. Buckle & D. R. Higgs, 2022. "On-microscope staging of live cells reveals changes in the dynamics of transcriptional bursting during differentiation," Nature Communications, Nature, vol. 13(1), pages 1-12, December.

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