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Activation and self-inactivation mechanisms of the cyclic oligoadenylate-dependent CRISPR ribonuclease Csm6
Bacterial and archaeal CRISPR-Cas systems provide RNA-guided immunity against genetic invaders such as bacteriophages and plasmids. Upon target RNA recognition, type III CRISPR-Cas systems produce cyclic-oligoadenylate second messengers that activate downstream effectors, including Csm6 ribonuclease...
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/PMC7101355/ https://www.ncbi.nlm.nih.gov/pubmed/32221291 http://dx.doi.org/10.1038/s41467-020-15334-5 |
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author | Garcia-Doval, Carmela Schwede, Frank Berk, Christian Rostøl, Jakob T. Niewoehner, Ole Tejero, Oliver Hall, Jonathan Marraffini, Luciano A. Jinek, Martin |
author_facet | Garcia-Doval, Carmela Schwede, Frank Berk, Christian Rostøl, Jakob T. Niewoehner, Ole Tejero, Oliver Hall, Jonathan Marraffini, Luciano A. Jinek, Martin |
author_sort | Garcia-Doval, Carmela |
collection | PubMed |
description | Bacterial and archaeal CRISPR-Cas systems provide RNA-guided immunity against genetic invaders such as bacteriophages and plasmids. Upon target RNA recognition, type III CRISPR-Cas systems produce cyclic-oligoadenylate second messengers that activate downstream effectors, including Csm6 ribonucleases, via their CARF domains. Here, we show that Enteroccocus italicus Csm6 (EiCsm6) degrades its cognate cyclic hexa-AMP (cA6) activator, and report the crystal structure of EiCsm6 bound to a cA6 mimic. Our structural, biochemical, and in vivo functional assays reveal how cA6 recognition by the CARF domain activates the Csm6 HEPN domains for collateral RNA degradation, and how CARF domain-mediated cA6 cleavage provides an intrinsic off-switch to limit Csm6 activity in the absence of ring nucleases. These mechanisms facilitate rapid invader clearance and ensure termination of CRISPR interference to limit self-toxicity. |
format | Online Article Text |
id | pubmed-7101355 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-71013552020-03-30 Activation and self-inactivation mechanisms of the cyclic oligoadenylate-dependent CRISPR ribonuclease Csm6 Garcia-Doval, Carmela Schwede, Frank Berk, Christian Rostøl, Jakob T. Niewoehner, Ole Tejero, Oliver Hall, Jonathan Marraffini, Luciano A. Jinek, Martin Nat Commun Article Bacterial and archaeal CRISPR-Cas systems provide RNA-guided immunity against genetic invaders such as bacteriophages and plasmids. Upon target RNA recognition, type III CRISPR-Cas systems produce cyclic-oligoadenylate second messengers that activate downstream effectors, including Csm6 ribonucleases, via their CARF domains. Here, we show that Enteroccocus italicus Csm6 (EiCsm6) degrades its cognate cyclic hexa-AMP (cA6) activator, and report the crystal structure of EiCsm6 bound to a cA6 mimic. Our structural, biochemical, and in vivo functional assays reveal how cA6 recognition by the CARF domain activates the Csm6 HEPN domains for collateral RNA degradation, and how CARF domain-mediated cA6 cleavage provides an intrinsic off-switch to limit Csm6 activity in the absence of ring nucleases. These mechanisms facilitate rapid invader clearance and ensure termination of CRISPR interference to limit self-toxicity. Nature Publishing Group UK 2020-03-27 /pmc/articles/PMC7101355/ /pubmed/32221291 http://dx.doi.org/10.1038/s41467-020-15334-5 Text en © The Author(s) 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 Garcia-Doval, Carmela Schwede, Frank Berk, Christian Rostøl, Jakob T. Niewoehner, Ole Tejero, Oliver Hall, Jonathan Marraffini, Luciano A. Jinek, Martin Activation and self-inactivation mechanisms of the cyclic oligoadenylate-dependent CRISPR ribonuclease Csm6 |
title | Activation and self-inactivation mechanisms of the cyclic oligoadenylate-dependent CRISPR ribonuclease Csm6 |
title_full | Activation and self-inactivation mechanisms of the cyclic oligoadenylate-dependent CRISPR ribonuclease Csm6 |
title_fullStr | Activation and self-inactivation mechanisms of the cyclic oligoadenylate-dependent CRISPR ribonuclease Csm6 |
title_full_unstemmed | Activation and self-inactivation mechanisms of the cyclic oligoadenylate-dependent CRISPR ribonuclease Csm6 |
title_short | Activation and self-inactivation mechanisms of the cyclic oligoadenylate-dependent CRISPR ribonuclease Csm6 |
title_sort | activation and self-inactivation mechanisms of the cyclic oligoadenylate-dependent crispr ribonuclease csm6 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7101355/ https://www.ncbi.nlm.nih.gov/pubmed/32221291 http://dx.doi.org/10.1038/s41467-020-15334-5 |
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