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Learning the histone codes with large genomic windows and three-dimensional chromatin interactions using transformer

Author

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  • Dohoon Lee

    (Seoul National University
    Seoul National University)

  • Jeewon Yang

    (Seoul National University)

  • Sun Kim

    (Seoul National University
    Seoul National University
    Seoul National University
    AIGENDRUG Co., Ltd.)

Abstract

The quantitative characterization of the transcriptional control by histone modifications has been challenged by many computational studies, but most of them only focus on narrow and linear genomic regions around promoters, leaving a room for improvement. We present Chromoformer, a transformer-based, three-dimensional chromatin conformation-aware deep learning architecture that achieves the state-of-the-art performance in the quantitative deciphering of the histone codes in gene regulation. The core essence of Chromoformer architecture lies in the three variants of attention operation, each specialized to model individual hierarchy of transcriptional regulation involving from core promoters to distal elements in contact with promoters through three-dimensional chromatin interactions. In-depth interpretation of Chromoformer reveals that it adaptively utilizes the long-range dependencies between histone modifications associated with transcription initiation and elongation. We also show that the quantitative kinetics of transcription factories and Polycomb group bodies can be captured by Chromoformer. Together, our study highlights the great advantage of attention-based deep modeling of complex interactions in epigenomes.

Suggested Citation

  • Dohoon Lee & Jeewon Yang & Sun Kim, 2022. "Learning the histone codes with large genomic windows and three-dimensional chromatin interactions using transformer," Nature Communications, Nature, vol. 13(1), pages 1-19, December.
  • Handle: RePEc:nat:natcom:v:13:y:2022:i:1:d:10.1038_s41467-022-34152-5
    DOI: 10.1038/s41467-022-34152-5
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    1. Kathryn Tunyasuvunakool & Jonas Adler & Zachary Wu & Tim Green & Michal Zielinski & Augustin Žídek & Alex Bridgland & Andrew Cowie & Clemens Meyer & Agata Laydon & Sameer Velankar & Gerard J. Kleywegt, 2021. "Highly accurate protein structure prediction for the human proteome," Nature, Nature, vol. 596(7873), pages 590-596, August.
    2. Yichao Cai & Ying Zhang & Yan Ping Loh & Jia Qi Tng & Mei Chee Lim & Zhendong Cao & Anandhkumar Raju & Erez Lieberman Aiden & Shang Li & Lakshmanan Manikandan & Vinay Tergaonkar & Greg Tucker-Kellogg , 2021. "H3K27me3-rich genomic regions can function as silencers to repress gene expression via chromatin interactions," Nature Communications, Nature, vol. 12(1), pages 1-22, December.
    3. John Jumper & Richard Evans & Alexander Pritzel & Tim Green & Michael Figurnov & Olaf Ronneberger & Kathryn Tunyasuvunakool & Russ Bates & Augustin Žídek & Anna Potapenko & Alex Bridgland & Clemens Me, 2021. "Highly accurate protein structure prediction with AlphaFold," Nature, Nature, vol. 596(7873), pages 583-589, August.
    4. Jesse R. Dixon & Siddarth Selvaraj & Feng Yue & Audrey Kim & Yan Li & Yin Shen & Ming Hu & Jun S. Liu & Bing Ren, 2012. "Topological domains in mammalian genomes identified by analysis of chromatin interactions," Nature, Nature, vol. 485(7398), pages 376-380, May.
    5. Nicolás Frankel & Gregory K. Davis & Diego Vargas & Shu Wang & François Payre & David L. Stern, 2010. "Phenotypic robustness conferred by apparently redundant transcriptional enhancers," Nature, Nature, vol. 466(7305), pages 490-493, July.
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