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Controlling gene expression with deep generative design of regulatory DNA

Author

Listed:
  • Jan Zrimec

    (Chalmers University of Technology
    National Institute of Biology)

  • Xiaozhi Fu

    (Chalmers University of Technology)

  • Azam Sheikh Muhammad

    (Chalmers University of Technology)

  • Christos Skrekas

    (Chalmers University of Technology)

  • Vykintas Jauniskis

    (Chalmers University of Technology
    Biomatter Designs)

  • Nora K. Speicher

    (Chalmers University of Technology)

  • Christoph S. Börlin

    (Chalmers University of Technology
    BioInnovation Institute)

  • Vilhelm Verendel

    (Chalmers University of Technology)

  • Morteza Haghir Chehreghani

    (Chalmers University of Technology)

  • Devdatt Dubhashi

    (Chalmers University of Technology)

  • Verena Siewers

    (Chalmers University of Technology)

  • Florian David

    (Chalmers University of Technology)

  • Jens Nielsen

    (Chalmers University of Technology
    BioInnovation Institute)

  • Aleksej Zelezniak

    (Chalmers University of Technology
    Vilnius University
    King’s College London)

Abstract

Design of de novo synthetic regulatory DNA is a promising avenue to control gene expression in biotechnology and medicine. Using mutagenesis typically requires screening sizable random DNA libraries, which limits the designs to span merely a short section of the promoter and restricts their control of gene expression. Here, we prototype a deep learning strategy based on generative adversarial networks (GAN) by learning directly from genomic and transcriptomic data. Our ExpressionGAN can traverse the entire regulatory sequence-expression landscape in a gene-specific manner, generating regulatory DNA with prespecified target mRNA levels spanning the whole gene regulatory structure including coding and adjacent non-coding regions. Despite high sequence divergence from natural DNA, in vivo measurements show that 57% of the highly-expressed synthetic sequences surpass the expression levels of highly-expressed natural controls. This demonstrates the applicability and relevance of deep generative design to expand our knowledge and control of gene expression regulation in any desired organism, condition or tissue.

Suggested Citation

  • Jan Zrimec & Xiaozhi Fu & Azam Sheikh Muhammad & Christos Skrekas & Vykintas Jauniskis & Nora K. Speicher & Christoph S. Börlin & Vilhelm Verendel & Morteza Haghir Chehreghani & Devdatt Dubhashi & Ver, 2022. "Controlling gene expression with deep generative design of regulatory DNA," Nature Communications, Nature, vol. 13(1), pages 1-17, December.
  • Handle: RePEc:nat:natcom:v:13:y:2022:i:1:d:10.1038_s41467-022-32818-8
    DOI: 10.1038/s41467-022-32818-8
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    References listed on IDEAS

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    Cited by:

    1. Pengcheng Zhang & Haochen Wang & Hanwen Xu & Lei Wei & Liyang Liu & Zhirui Hu & Xiaowo Wang, 2023. "Deep flanking sequence engineering for efficient promoter design using DeepSEED," Nature Communications, Nature, vol. 14(1), pages 1-14, December.
    2. Evangelos-Marios Nikolados & Arin Wongprommoon & Oisin Mac Aodha & Guillaume Cambray & Diego A. Oyarzún, 2022. "Accuracy and data efficiency in deep learning models of protein expression," Nature Communications, Nature, vol. 13(1), pages 1-12, December.

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