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Widespread anti-CRISPR proteins in virulent bacteriophages inhibit a range of Cas9 proteins
CRISPR-Cas systems are bacterial anti-viral systems, and bacterial viruses (bacteriophages, phages) can carry anti-CRISPR (Acr) proteins to evade that immunity. Acrs can also fine-tune the activity of CRISPR-based genome-editing tools. While Acrs are prevalent in phages capable of lying dormant in a...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6060171/ https://www.ncbi.nlm.nih.gov/pubmed/30046034 http://dx.doi.org/10.1038/s41467-018-05092-w |
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author | Hynes, Alexander P. Rousseau, Geneviève M. Agudelo, Daniel Goulet, Adeline Amigues, Beatrice Loehr, Jeremy Romero, Dennis A. Fremaux, Christophe Horvath, Philippe Doyon, Yannick Cambillau, Christian Moineau, Sylvain |
author_facet | Hynes, Alexander P. Rousseau, Geneviève M. Agudelo, Daniel Goulet, Adeline Amigues, Beatrice Loehr, Jeremy Romero, Dennis A. Fremaux, Christophe Horvath, Philippe Doyon, Yannick Cambillau, Christian Moineau, Sylvain |
author_sort | Hynes, Alexander P. |
collection | PubMed |
description | CRISPR-Cas systems are bacterial anti-viral systems, and bacterial viruses (bacteriophages, phages) can carry anti-CRISPR (Acr) proteins to evade that immunity. Acrs can also fine-tune the activity of CRISPR-based genome-editing tools. While Acrs are prevalent in phages capable of lying dormant in a CRISPR-carrying host, their orthologs have been observed only infrequently in virulent phages. Here we identify AcrIIA6, an Acr encoded in 33% of virulent Streptococcus thermophilus phage genomes. The X-ray structure of AcrIIA6 displays some features unique to this Acr family. We compare the activity of AcrIIA6 to those of other Acrs, including AcrIIA5 (also from S. thermophilus phages), and characterize their effectiveness against a range of CRISPR-Cas systems. Finally, we demonstrate that both Acr families from S. thermophilus phages inhibit Cas9-mediated genome editing of human cells. |
format | Online Article Text |
id | pubmed-6060171 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-60601712018-07-27 Widespread anti-CRISPR proteins in virulent bacteriophages inhibit a range of Cas9 proteins Hynes, Alexander P. Rousseau, Geneviève M. Agudelo, Daniel Goulet, Adeline Amigues, Beatrice Loehr, Jeremy Romero, Dennis A. Fremaux, Christophe Horvath, Philippe Doyon, Yannick Cambillau, Christian Moineau, Sylvain Nat Commun Article CRISPR-Cas systems are bacterial anti-viral systems, and bacterial viruses (bacteriophages, phages) can carry anti-CRISPR (Acr) proteins to evade that immunity. Acrs can also fine-tune the activity of CRISPR-based genome-editing tools. While Acrs are prevalent in phages capable of lying dormant in a CRISPR-carrying host, their orthologs have been observed only infrequently in virulent phages. Here we identify AcrIIA6, an Acr encoded in 33% of virulent Streptococcus thermophilus phage genomes. The X-ray structure of AcrIIA6 displays some features unique to this Acr family. We compare the activity of AcrIIA6 to those of other Acrs, including AcrIIA5 (also from S. thermophilus phages), and characterize their effectiveness against a range of CRISPR-Cas systems. Finally, we demonstrate that both Acr families from S. thermophilus phages inhibit Cas9-mediated genome editing of human cells. Nature Publishing Group UK 2018-07-25 /pmc/articles/PMC6060171/ /pubmed/30046034 http://dx.doi.org/10.1038/s41467-018-05092-w Text en © The Author(s) 2018 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 Hynes, Alexander P. Rousseau, Geneviève M. Agudelo, Daniel Goulet, Adeline Amigues, Beatrice Loehr, Jeremy Romero, Dennis A. Fremaux, Christophe Horvath, Philippe Doyon, Yannick Cambillau, Christian Moineau, Sylvain Widespread anti-CRISPR proteins in virulent bacteriophages inhibit a range of Cas9 proteins |
title | Widespread anti-CRISPR proteins in virulent bacteriophages inhibit a range of Cas9 proteins |
title_full | Widespread anti-CRISPR proteins in virulent bacteriophages inhibit a range of Cas9 proteins |
title_fullStr | Widespread anti-CRISPR proteins in virulent bacteriophages inhibit a range of Cas9 proteins |
title_full_unstemmed | Widespread anti-CRISPR proteins in virulent bacteriophages inhibit a range of Cas9 proteins |
title_short | Widespread anti-CRISPR proteins in virulent bacteriophages inhibit a range of Cas9 proteins |
title_sort | widespread anti-crispr proteins in virulent bacteriophages inhibit a range of cas9 proteins |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6060171/ https://www.ncbi.nlm.nih.gov/pubmed/30046034 http://dx.doi.org/10.1038/s41467-018-05092-w |
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