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Type IV CRISPR–Cas systems are highly diverse and involved in competition between plasmids
CRISPR–Cas systems provide prokaryotes with adaptive immune functions against viruses and other genetic parasites. In contrast to all other types of CRISPR–Cas systems, type IV has remained largely overlooked. Here, we describe a previously uncharted diversity of type IV gene cassettes, primarily en...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7038947/ https://www.ncbi.nlm.nih.gov/pubmed/31879772 http://dx.doi.org/10.1093/nar/gkz1197 |
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author | Pinilla-Redondo, Rafael Mayo-Muñoz, David Russel, Jakob Garrett, Roger A Randau, Lennart Sørensen, Søren J Shah, Shiraz A |
author_facet | Pinilla-Redondo, Rafael Mayo-Muñoz, David Russel, Jakob Garrett, Roger A Randau, Lennart Sørensen, Søren J Shah, Shiraz A |
author_sort | Pinilla-Redondo, Rafael |
collection | PubMed |
description | CRISPR–Cas systems provide prokaryotes with adaptive immune functions against viruses and other genetic parasites. In contrast to all other types of CRISPR–Cas systems, type IV has remained largely overlooked. Here, we describe a previously uncharted diversity of type IV gene cassettes, primarily encoded by plasmid-like elements from diverse prokaryotic taxa. Remarkably, via a comprehensive analysis of their CRISPR spacer content, these systems were found to exhibit a strong bias towards the targeting of other plasmids. Our data indicate that the functions of type IV systems have diverged from those of other host-related CRISPR–Cas immune systems to adopt a role in mediating conflicts between plasmids. Furthermore, we find evidence for cross-talk between certain type IV and type I CRISPR–Cas systems that co-exist intracellularly, thus providing a simple answer to the enigmatic absence of type IV adaptation modules. Collectively, our results lead to the expansion and reclassification of type IV systems and provide novel insights into the biological function and evolution of these elusive systems. |
format | Online Article Text |
id | pubmed-7038947 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-70389472020-03-02 Type IV CRISPR–Cas systems are highly diverse and involved in competition between plasmids Pinilla-Redondo, Rafael Mayo-Muñoz, David Russel, Jakob Garrett, Roger A Randau, Lennart Sørensen, Søren J Shah, Shiraz A Nucleic Acids Res Molecular Biology CRISPR–Cas systems provide prokaryotes with adaptive immune functions against viruses and other genetic parasites. In contrast to all other types of CRISPR–Cas systems, type IV has remained largely overlooked. Here, we describe a previously uncharted diversity of type IV gene cassettes, primarily encoded by plasmid-like elements from diverse prokaryotic taxa. Remarkably, via a comprehensive analysis of their CRISPR spacer content, these systems were found to exhibit a strong bias towards the targeting of other plasmids. Our data indicate that the functions of type IV systems have diverged from those of other host-related CRISPR–Cas immune systems to adopt a role in mediating conflicts between plasmids. Furthermore, we find evidence for cross-talk between certain type IV and type I CRISPR–Cas systems that co-exist intracellularly, thus providing a simple answer to the enigmatic absence of type IV adaptation modules. Collectively, our results lead to the expansion and reclassification of type IV systems and provide novel insights into the biological function and evolution of these elusive systems. Oxford University Press 2020-02-28 2019-12-27 /pmc/articles/PMC7038947/ /pubmed/31879772 http://dx.doi.org/10.1093/nar/gkz1197 Text en © The Author(s) 2019. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Molecular Biology Pinilla-Redondo, Rafael Mayo-Muñoz, David Russel, Jakob Garrett, Roger A Randau, Lennart Sørensen, Søren J Shah, Shiraz A Type IV CRISPR–Cas systems are highly diverse and involved in competition between plasmids |
title | Type IV CRISPR–Cas systems are highly diverse and involved in competition between plasmids |
title_full | Type IV CRISPR–Cas systems are highly diverse and involved in competition between plasmids |
title_fullStr | Type IV CRISPR–Cas systems are highly diverse and involved in competition between plasmids |
title_full_unstemmed | Type IV CRISPR–Cas systems are highly diverse and involved in competition between plasmids |
title_short | Type IV CRISPR–Cas systems are highly diverse and involved in competition between plasmids |
title_sort | type iv crispr–cas systems are highly diverse and involved in competition between plasmids |
topic | Molecular Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7038947/ https://www.ncbi.nlm.nih.gov/pubmed/31879772 http://dx.doi.org/10.1093/nar/gkz1197 |
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