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Machine-learning approach expands the repertoire of anti-CRISPR protein families
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)...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7391736/ https://www.ncbi.nlm.nih.gov/pubmed/32728052 http://dx.doi.org/10.1038/s41467-020-17652-0 |
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author | Gussow, Ayal B. Park, Allyson E. Borges, Adair L. Shmakov, Sergey A. Makarova, Kira S. Wolf, Yuri I. Bondy-Denomy, Joseph Koonin, Eugene V. |
author_facet | Gussow, Ayal B. Park, Allyson E. Borges, Adair L. Shmakov, Sergey A. Makarova, Kira S. Wolf, Yuri I. Bondy-Denomy, Joseph Koonin, Eugene V. |
author_sort | Gussow, Ayal B. |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-7391736 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-73917362020-08-12 Machine-learning approach expands the repertoire of anti-CRISPR protein families Gussow, Ayal B. Park, Allyson E. Borges, Adair L. Shmakov, Sergey A. Makarova, Kira S. Wolf, Yuri I. Bondy-Denomy, Joseph Koonin, Eugene V. Nat Commun Article 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. Nature Publishing Group UK 2020-07-29 /pmc/articles/PMC7391736/ /pubmed/32728052 http://dx.doi.org/10.1038/s41467-020-17652-0 Text en © This is a U.S. government work and not under copyright protection in the U.S.; foreign copyright protection may apply 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Gussow, Ayal B. Park, Allyson E. Borges, Adair L. Shmakov, Sergey A. Makarova, Kira S. Wolf, Yuri I. Bondy-Denomy, Joseph Koonin, Eugene V. Machine-learning approach expands the repertoire of anti-CRISPR protein families |
title | Machine-learning approach expands the repertoire of anti-CRISPR protein families |
title_full | Machine-learning approach expands the repertoire of anti-CRISPR protein families |
title_fullStr | Machine-learning approach expands the repertoire of anti-CRISPR protein families |
title_full_unstemmed | Machine-learning approach expands the repertoire of anti-CRISPR protein families |
title_short | Machine-learning approach expands the repertoire of anti-CRISPR protein families |
title_sort | machine-learning approach expands the repertoire of anti-crispr protein families |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7391736/ https://www.ncbi.nlm.nih.gov/pubmed/32728052 http://dx.doi.org/10.1038/s41467-020-17652-0 |
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