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Bacteriophages suppress CRISPR–Cas immunity using RNA-based anti-CRISPRs
Many bacteria use CRISPR–Cas systems to combat mobile genetic elements, such as bacteriophages and plasmids(1). In turn, these invasive elements have evolved anti-CRISPR proteins to block host immunity(2,3). Here we unveil a distinct type of CRISPR–Cas Inhibition strategy that is based on small non-...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10651486/ https://www.ncbi.nlm.nih.gov/pubmed/37853129 http://dx.doi.org/10.1038/s41586-023-06612-5 |
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author | Camara-Wilpert, Sarah Mayo-Muñoz, David Russel, Jakob Fagerlund, Robert D. Madsen, Jonas S. Fineran, Peter C. Sørensen, Søren J. Pinilla-Redondo, Rafael |
author_facet | Camara-Wilpert, Sarah Mayo-Muñoz, David Russel, Jakob Fagerlund, Robert D. Madsen, Jonas S. Fineran, Peter C. Sørensen, Søren J. Pinilla-Redondo, Rafael |
author_sort | Camara-Wilpert, Sarah |
collection | PubMed |
description | Many bacteria use CRISPR–Cas systems to combat mobile genetic elements, such as bacteriophages and plasmids(1). In turn, these invasive elements have evolved anti-CRISPR proteins to block host immunity(2,3). Here we unveil a distinct type of CRISPR–Cas Inhibition strategy that is based on small non-coding RNA anti-CRISPRs (Racrs). Racrs mimic the repeats found in CRISPR arrays and are encoded in viral genomes as solitary repeat units(4). We show that a prophage-encoded Racr strongly inhibits the type I-F CRISPR–Cas system by interacting specifically with Cas6f and Cas7f, resulting in the formation of an aberrant Cas subcomplex. We identified Racr candidates for almost all CRISPR–Cas types encoded by a diverse range of viruses and plasmids, often in the genetic context of other anti-CRISPR genes(5). Functional testing of nine candidates spanning the two CRISPR–Cas classes confirmed their strong immune inhibitory function. Our results demonstrate that molecular mimicry of CRISPR repeats is a widespread anti-CRISPR strategy, which opens the door to potential biotechnological applications(6). |
format | Online Article Text |
id | pubmed-10651486 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-106514862023-10-18 Bacteriophages suppress CRISPR–Cas immunity using RNA-based anti-CRISPRs Camara-Wilpert, Sarah Mayo-Muñoz, David Russel, Jakob Fagerlund, Robert D. Madsen, Jonas S. Fineran, Peter C. Sørensen, Søren J. Pinilla-Redondo, Rafael Nature Article Many bacteria use CRISPR–Cas systems to combat mobile genetic elements, such as bacteriophages and plasmids(1). In turn, these invasive elements have evolved anti-CRISPR proteins to block host immunity(2,3). Here we unveil a distinct type of CRISPR–Cas Inhibition strategy that is based on small non-coding RNA anti-CRISPRs (Racrs). Racrs mimic the repeats found in CRISPR arrays and are encoded in viral genomes as solitary repeat units(4). We show that a prophage-encoded Racr strongly inhibits the type I-F CRISPR–Cas system by interacting specifically with Cas6f and Cas7f, resulting in the formation of an aberrant Cas subcomplex. We identified Racr candidates for almost all CRISPR–Cas types encoded by a diverse range of viruses and plasmids, often in the genetic context of other anti-CRISPR genes(5). Functional testing of nine candidates spanning the two CRISPR–Cas classes confirmed their strong immune inhibitory function. Our results demonstrate that molecular mimicry of CRISPR repeats is a widespread anti-CRISPR strategy, which opens the door to potential biotechnological applications(6). Nature Publishing Group UK 2023-10-18 2023 /pmc/articles/PMC10651486/ /pubmed/37853129 http://dx.doi.org/10.1038/s41586-023-06612-5 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Camara-Wilpert, Sarah Mayo-Muñoz, David Russel, Jakob Fagerlund, Robert D. Madsen, Jonas S. Fineran, Peter C. Sørensen, Søren J. Pinilla-Redondo, Rafael Bacteriophages suppress CRISPR–Cas immunity using RNA-based anti-CRISPRs |
title | Bacteriophages suppress CRISPR–Cas immunity using RNA-based anti-CRISPRs |
title_full | Bacteriophages suppress CRISPR–Cas immunity using RNA-based anti-CRISPRs |
title_fullStr | Bacteriophages suppress CRISPR–Cas immunity using RNA-based anti-CRISPRs |
title_full_unstemmed | Bacteriophages suppress CRISPR–Cas immunity using RNA-based anti-CRISPRs |
title_short | Bacteriophages suppress CRISPR–Cas immunity using RNA-based anti-CRISPRs |
title_sort | bacteriophages suppress crispr–cas immunity using rna-based anti-crisprs |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10651486/ https://www.ncbi.nlm.nih.gov/pubmed/37853129 http://dx.doi.org/10.1038/s41586-023-06612-5 |
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