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A predominant enhancer co-amplified with the SOX2 oncogene is necessary and sufficient for its expression in squamous cancer

Author

Listed:
  • Yanli Liu

    (Fudan University
    University of Utah
    Northwest Agriculture and Forestry University)

  • Zhong Wu

    (Sichuan University
    Harvard Medical School)

  • Jin Zhou

    (Sichuan University
    Harvard Medical School)

  • Dinesh K. A. Ramadurai

    (University of Utah)

  • Katelyn L. Mortenson

    (University of Utah)

  • Estrella Aguilera-Jimenez

    (University of Utah)

  • Yifei Yan

    (Research Institute of the McGill University Health Centre
    McGill University)

  • Xiaojun Yang

    (Northwest Agriculture and Forestry University)

  • Alison M. Taylor

    (Columbia University)

  • Katherine E. Varley

    (University of Utah)

  • Jason Gertz

    (University of Utah)

  • Peter S. Choi

    (University of Pennsylvania)

  • Andrew D. Cherniack

    (Harvard Medical School
    Broad Institute of MIT and Harvard)

  • Xingdong Chen

    (Fudan University
    Fudan University Taizhou Institute of Health Sciences
    Yiwu Research Institute of Fudan University)

  • Adam J. Bass

    (Harvard Medical School
    Broad Institute of MIT and Harvard
    Columbia University)

  • Swneke D. Bailey

    (Research Institute of the McGill University Health Centre
    McGill University)

  • Xiaoyang Zhang

    (Fudan University
    University of Utah)

Abstract

Amplification and overexpression of the SOX2 oncogene represent a hallmark of squamous cancers originating from diverse tissue types. Here, we find that squamous cancers selectively amplify a 3’ noncoding region together with SOX2, which harbors squamous cancer-specific chromatin accessible regions. We identify a single enhancer e1 that predominantly drives SOX2 expression. Repression of e1 in SOX2-high cells causes collapse of the surrounding enhancers, remarkable reduction in SOX2 expression, and a global transcriptional change reminiscent of SOX2 knockout. The e1 enhancer is driven by a combination of transcription factors including SOX2 itself and the AP-1 complex, which facilitates recruitment of the co-activator BRD4. CRISPR-mediated activation of e1 in SOX2-low cells is sufficient to rebuild the e1-SOX2 loop and activate SOX2 expression. Our study shows that squamous cancers selectively amplify a predominant enhancer to drive SOX2 overexpression, uncovering functional links among enhancer activation, chromatin looping, and lineage-specific copy number amplifications of oncogenes.

Suggested Citation

  • Yanli Liu & Zhong Wu & Jin Zhou & Dinesh K. A. Ramadurai & Katelyn L. Mortenson & Estrella Aguilera-Jimenez & Yifei Yan & Xiaojun Yang & Alison M. Taylor & Katherine E. Varley & Jason Gertz & Peter S., 2021. "A predominant enhancer co-amplified with the SOX2 oncogene is necessary and sufficient for its expression in squamous cancer," Nature Communications, Nature, vol. 12(1), pages 1-14, December.
  • Handle: RePEc:nat:natcom:v:12:y:2021:i:1:d:10.1038_s41467-021-27055-4
    DOI: 10.1038/s41467-021-27055-4
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