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

被引:61
|
作者
Gussow, Ayal B. [1 ]
Park, Allyson E. [2 ]
Borges, Adair L. [2 ]
Shmakov, Sergey A. [1 ]
Makarova, Kira S. [1 ]
Wolf, Yuri I. [1 ]
Bondy-Denomy, Joseph [2 ]
Koonin, Eugene V. [1 ]
机构
[1] NIH, Natl Ctr Biotechnol Informat, Natl Lib Med, Bethesda, MD 20894 USA
[2] Univ Calif San Francisco, Dept Microbiol & Immunol, San Francisco, CA 94143 USA
关键词
INHIBITION; MECHANISM; CLASSIFICATION; EVOLUTION; DISCOVERY; RESOURCE; GENOMICS;
D O I
10.1038/s41467-020-17652-0
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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.
引用
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页数:12
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