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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
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.
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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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