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MLL-AF4 cooperates with PAF1 and FACT to drive high-density enhancer interactions in leukemia

Author

Listed:
  • Nicholas T. Crump

    (University of Oxford
    Imperial College London)

  • Alastair L. Smith

    (University of Oxford)

  • Laura Godfrey

    (University of Oxford)

  • Ana M. Dopico-Fernandez

    (University of Oxford)

  • Nicholas Denny

    (University of Oxford)

  • Joe R. Harman

    (University of Oxford)

  • Joseph C. Hamley

    (University of Oxford)

  • Nicole E. Jackson

    (University of Oxford)

  • Catherine Chahrour

    (University of Oxford)

  • Simone Riva

    (University of Oxford)

  • Siobhan Rice

    (University of Oxford)

  • Jaehoon Kim

    (Korea Advanced Institute of Science and Technology)

  • Venkatesha Basrur

    (University of Michigan)

  • Damian Fermin

    (University of Michigan)

  • Kojo Elenitoba-Johnson

    (University of Pennsylvania)

  • Robert G. Roeder

    (The Rockefeller University)

  • C. David Allis

    (The Rockefeller University)

  • Irene Roberts

    (University of Oxford
    University of Oxford)

  • Anindita Roy

    (University of Oxford
    University of Oxford)

  • Huimin Geng

    (University of California, San Francisco, San Francisco)

  • James O. J. Davies

    (University of Oxford)

  • Thomas A. Milne

    (University of Oxford)

Abstract

Aberrant enhancer activation is a key mechanism driving oncogene expression in many cancers. While much is known about the regulation of larger chromosome domains in eukaryotes, the details of enhancer-promoter interactions remain poorly understood. Recent work suggests co-activators like BRD4 and Mediator have little impact on enhancer-promoter interactions. In leukemias controlled by the MLL-AF4 fusion protein, we use the ultra-high resolution technique Micro-Capture-C (MCC) to show that MLL-AF4 binding promotes broad, high-density regions of enhancer-promoter interactions at a subset of key targets. These enhancers are enriched for transcription elongation factors like PAF1C and FACT, and the loss of these factors abolishes enhancer-promoter contact. This work not only provides an additional model for how MLL-AF4 is able to drive high levels of transcription at key genes in leukemia but also suggests a more general model linking enhancer-promoter crosstalk and transcription elongation.

Suggested Citation

  • Nicholas T. Crump & Alastair L. Smith & Laura Godfrey & Ana M. Dopico-Fernandez & Nicholas Denny & Joe R. Harman & Joseph C. Hamley & Nicole E. Jackson & Catherine Chahrour & Simone Riva & Siobhan Ric, 2023. "MLL-AF4 cooperates with PAF1 and FACT to drive high-density enhancer interactions in leukemia," Nature Communications, Nature, vol. 14(1), pages 1-20, December.
  • Handle: RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-40981-9
    DOI: 10.1038/s41467-023-40981-9
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    References listed on IDEAS

    as
    1. Alvaro Rada-Iglesias & Ruchi Bajpai & Tomek Swigut & Samantha A. Brugmann & Ryan A. Flynn & Joanna Wysocka, 2011. "A unique chromatin signature uncovers early developmental enhancers in humans," Nature, Nature, vol. 470(7333), pages 279-283, February.
    2. 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.
    3. Irene Robles-Rebollo & Sergi Cuartero & Adria Canellas-Socias & Sarah Wells & Mohammad M. Karimi & Elisabetta Mereu & Alexandra G. Chivu & Holger Heyn & Chad Whilding & Dirk Dormann & Samuel Marguerat, 2022. "Cohesin couples transcriptional bursting probabilities of inducible enhancers and promoters," Nature Communications, Nature, vol. 13(1), pages 1-16, December.
    4. Laura Godfrey & Nicholas T. Crump & Ross Thorne & I-Jun Lau & Emmanouela Repapi & Dimitra Dimou & Alastair L. Smith & Joe R. Harman & Jelena M. Telenius & A. Marieke Oudelaar & Damien J. Downes & Pare, 2019. "DOT1L inhibition reveals a distinct subset of enhancers dependent on H3K79 methylation," Nature Communications, Nature, vol. 10(1), pages 1-15, December.
    Full references (including those not matched with items on IDEAS)

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