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Machine-learning approach expands the repertoire of anti-CRISPR protein families

Author

Listed:
  • Ayal B. Gussow

    (National Institutes of Health)

  • Allyson E. Park

    (University of California San Francisco)

  • Adair L. Borges

    (University of California San Francisco)

  • Sergey A. Shmakov

    (National Institutes of Health)

  • Kira S. Makarova

    (National Institutes of Health)

  • Yuri I. Wolf

    (National Institutes of Health)

  • Joseph Bondy-Denomy

    (University of California San Francisco)

  • Eugene V. Koonin

    (National Institutes of Health)

Abstract

The CRISPR-Cas are adaptive bacterial and archaeal immunity systems that have been harnessed for the development of powerful genome editing and engineering tools. In the incessant host-parasite arms race, viruses evolved multiple anti-defense mechanisms including diverse anti-CRISPR proteins (Acrs) that specifically inhibit CRISPR-Cas and therefore have enormous potential for application as modulators of genome editing tools. Most Acrs are small and highly variable proteins which makes their bioinformatic prediction a formidable task. We present a machine-learning approach for comprehensive Acr prediction. The model shows high predictive power when tested against an unseen test set and was employed to predict 2,500 candidate Acr families. Experimental validation of top candidates revealed two unknown Acrs (AcrIC9, IC10) and three other top candidates were coincidentally identified and found to possess anti-CRISPR activity. These results substantially expand the repertoire of predicted Acrs and provide a resource for experimental Acr discovery.

Suggested Citation

  • Ayal B. Gussow & Allyson E. Park & Adair L. Borges & Sergey A. Shmakov & Kira S. Makarova & Yuri I. Wolf & Joseph Bondy-Denomy & Eugene V. Koonin, 2020. "Machine-learning approach expands the repertoire of anti-CRISPR protein families," Nature Communications, Nature, vol. 11(1), pages 1-12, December.
  • Handle: RePEc:nat:natcom:v:11:y:2020:i:1:d:10.1038_s41467-020-17652-0
    DOI: 10.1038/s41467-020-17652-0
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    Cited by:

    1. Yuvaraj Bhoobalan-Chitty & Shuanshuan Xu & Laura Martinez-Alvarez & Svetlana Karamycheva & Kira S. Makarova & Eugene V. Koonin & Xu Peng, 2024. "Regulatory sequence-based discovery of anti-defense genes in archaeal viruses," Nature Communications, Nature, vol. 15(1), pages 1-13, December.
    2. Amir Pandi & Christoph Diehl & Ali Yazdizadeh Kharrazi & Scott A. Scholz & Elizaveta Bobkova & Léon Faure & Maren Nattermann & David Adam & Nils Chapin & Yeganeh Foroughijabbari & Charles Moritz & Nic, 2022. "A versatile active learning workflow for optimization of genetic and metabolic networks," Nature Communications, Nature, vol. 13(1), pages 1-15, December.
    3. Snehi Shrestha & Kieran James Barvenik & Tianle Chen & Haochen Yang & Yang Li & Meera Muthachi Kesavan & Joshua M. Little & Hayden C. Whitley & Zi Teng & Yaguang Luo & Eleonora Tubaldi & Po-Yen Chen, 2024. "Machine intelligence accelerated design of conductive MXene aerogels with programmable properties," Nature Communications, Nature, vol. 15(1), pages 1-14, December.

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