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Comprehensive 3D epigenomic maps define limbal stem/progenitor cell function and identity

Author

Listed:
  • Mingsen Li

    (Sun Yat-sen University)

  • Huaxing Huang

    (Sun Yat-sen University)

  • Bofeng Wang

    (Sun Yat-sen University)

  • Shaoshuai Jiang

    (Sun Yat-Sen University)

  • Huizhen Guo

    (Sun Yat-sen University)

  • Liqiong Zhu

    (Sun Yat-sen University)

  • Siqi Wu

    (Sun Yat-sen University)

  • Jiafeng Liu

    (Sun Yat-sen University)

  • Li Wang

    (Sun Yat-sen University)

  • Xihong Lan

    (Sun Yat-sen University)

  • Wang Zhang

    (Sun Yat-sen University)

  • Jin Zhu

    (Sun Yat-sen University)

  • Fuxi Li

    (Sun Yat-sen University)

  • Jieying Tan

    (Sun Yat-sen University)

  • Zhen Mao

    (Sun Yat-sen University)

  • Chunqiao Liu

    (Sun Yat-sen University)

  • Jianping Ji

    (Sun Yat-sen University)

  • Junjun Ding

    (Sun Yat-Sen University)

  • Kang Zhang

    (Macau University of Science and Technology)

  • Jin Yuan

    (Sun Yat-sen University)

  • Yizhi Liu

    (Sun Yat-sen University)

  • Hong Ouyang

    (Sun Yat-sen University
    Sun Yat-Sen University)

Abstract

The insights into how genome topology couples with epigenetic states to govern the function and identity of the corneal epithelium are poorly understood. Here, we generate a high-resolution Hi-C interaction map of human limbal stem/progenitor cells (LSCs) and show that chromatin multi-hierarchical organisation is coupled to gene expression. By integrating Hi-C, epigenome and transcriptome data, we characterize the comprehensive 3D epigenomic landscapes of LSCs. We find that super-silencers mediate gene repression associated with corneal development, differentiation and disease via chromatin looping and/or proximity. Super-enhancer (SE) interaction analysis identified a set of SE interactive hubs that contribute to LSC-specific gene activation. These active and inactive element-anchored loop networks occur within the cohesin-occupied CTCF-CTCF loops. We further reveal a coordinated regulatory network of core transcription factors based on SE-promoter interactions. Our results provide detailed insights into the genome organization principle for epigenetic regulation of gene expression in stratified epithelia.

Suggested Citation

  • Mingsen Li & Huaxing Huang & Bofeng Wang & Shaoshuai Jiang & Huizhen Guo & Liqiong Zhu & Siqi Wu & Jiafeng Liu & Li Wang & Xihong Lan & Wang Zhang & Jin Zhu & Fuxi Li & Jieying Tan & Zhen Mao & Chunqi, 2022. "Comprehensive 3D epigenomic maps define limbal stem/progenitor cell function and identity," Nature Communications, Nature, vol. 13(1), pages 1-16, December.
  • Handle: RePEc:nat:natcom:v:13:y:2022:i:1:d:10.1038_s41467-022-28966-6
    DOI: 10.1038/s41467-022-28966-6
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