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Machine learning uncovers cell identity regulator by histone code

Author

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  • Bo Xia

    (Houston Methodist Research Institute
    Houston Methodist Research Institute
    Cornell University
    Houston Methodist Research Institute)

  • Dongyu Zhao

    (Houston Methodist Research Institute
    Houston Methodist Research Institute
    Cornell University
    Houston Methodist Research Institute)

  • Guangyu Wang

    (Houston Methodist Research Institute
    Houston Methodist Research Institute
    Cornell University
    Houston Methodist Research Institute)

  • Min Zhang

    (Houston Methodist Research Institute
    Cornell University
    Houston Methodist Research Institute)

  • Jie Lv

    (Houston Methodist Research Institute
    Houston Methodist Research Institute
    Cornell University
    Houston Methodist Research Institute)

  • Alin S. Tomoiaga

    (Manhattan College)

  • Yanqiang Li

    (Houston Methodist Research Institute
    Houston Methodist Research Institute
    Cornell University
    Houston Methodist Research Institute)

  • Xin Wang

    (Houston Methodist Research Institute
    Houston Methodist Research Institute
    Cornell University
    Houston Methodist Research Institute)

  • Shu Meng

    (Houston Methodist Research Institute
    Cornell University
    Houston Methodist Research Institute)

  • John P. Cooke

    (Houston Methodist Research Institute
    Cornell University
    Houston Methodist Research Institute)

  • Qi Cao

    (Robert H. Lurie Comprehensive Cancer Center)

  • Lili Zhang

    (Houston Methodist Research Institute
    Cornell University
    Houston Methodist Research Institute)

  • Kaifu Chen

    (Houston Methodist Research Institute
    Houston Methodist Research Institute
    Cornell University
    Houston Methodist Research Institute)

Abstract

Conversion between cell types, e.g., by induced expression of master transcription factors, holds great promise for cellular therapy. Our ability to manipulate cell identity is constrained by incomplete information on cell identity genes (CIGs) and their expression regulation. Here, we develop CEFCIG, an artificial intelligent framework to uncover CIGs and further define their master regulators. On the basis of machine learning, CEFCIG reveals unique histone codes for transcriptional regulation of reported CIGs, and utilizes these codes to predict CIGs and their master regulators with high accuracy. Applying CEFCIG to 1,005 epigenetic profiles, our analysis uncovers the landscape of regulation network for identity genes in individual cell or tissue types. Together, this work provides insights into cell identity regulation, and delivers a powerful technique to facilitate regenerative medicine.

Suggested Citation

  • Bo Xia & Dongyu Zhao & Guangyu Wang & Min Zhang & Jie Lv & Alin S. Tomoiaga & Yanqiang Li & Xin Wang & Shu Meng & John P. Cooke & Qi Cao & Lili Zhang & Kaifu Chen, 2020. "Machine learning uncovers cell identity regulator by histone code," Nature Communications, Nature, vol. 11(1), pages 1-12, December.
  • Handle: RePEc:nat:natcom:v:11:y:2020:i:1:d:10.1038_s41467-020-16539-4
    DOI: 10.1038/s41467-020-16539-4
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    Cited by:

    1. Jie Lv & Shu Meng & Qilin Gu & Rongbin Zheng & Xinlei Gao & Jun-dae Kim & Min Chen & Bo Xia & Yihan Zuo & Sen Zhu & Dongyu Zhao & Yanqiang Li & Guangyu Wang & Xin Wang & Qingshu Meng & Qi Cao & John P, 2023. "Epigenetic landscape reveals MECOM as an endothelial lineage regulator," Nature Communications, Nature, vol. 14(1), pages 1-17, December.
    2. Marie Bobowski-Gerard & Clémence Boulet & Francesco P. Zummo & Julie Dubois-Chevalier & Céline Gheeraert & Mohamed Bou Saleh & Jean-Marc Strub & Amaury Farce & Maheul Ploton & Loïc Guille & Jimmy Vand, 2022. "Functional genomics uncovers the transcription factor BNC2 as required for myofibroblastic activation in fibrosis," Nature Communications, Nature, vol. 13(1), pages 1-20, December.

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