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It is unclear how important CRISPR-Cas systems are for protecting natural populations of bacteria against infections by mobile genetic elements
Articles on CRISPR commonly open with some variant of the phrase “these short palindromic repeats and their associated endonucleases (Cas) are an adaptive immune system that exists to protect bacteria and archaea from viruses and infections with other mobile genetic elements.” There is an abundance...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
National Academy of Sciences
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7668106/ https://www.ncbi.nlm.nih.gov/pubmed/33122438 http://dx.doi.org/10.1073/pnas.1915966117 |
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author | Westra, Edze R. Levin, Bruce R. |
author_facet | Westra, Edze R. Levin, Bruce R. |
author_sort | Westra, Edze R. |
collection | PubMed |
description | Articles on CRISPR commonly open with some variant of the phrase “these short palindromic repeats and their associated endonucleases (Cas) are an adaptive immune system that exists to protect bacteria and archaea from viruses and infections with other mobile genetic elements.” There is an abundance of genomic data consistent with the hypothesis that CRISPR plays this role in natural populations of bacteria and archaea, and experimental demonstrations with a few species of bacteria and their phage and plasmids show that CRISPR-Cas systems can play this role in vitro. Not at all clear are the ubiquity, magnitude, and nature of the contribution of CRISPR-Cas systems to the ecology and evolution of natural populations of microbes and the strength of selection mediated by different types of phage and plasmids to the evolution and maintenance of CRISPR-Cas systems. In this perspective, with the aid of heuristic mathematical–computer simulation models, we explore the a priori conditions under which exposure to lytic and temperate phage and conjugative plasmids will select for and maintain CRISPR-Cas systems in populations of bacteria and archaea. We review the existing literature addressing these ecological and evolutionary questions and highlight the experimental and other evidence needed to fully understand the conditions responsible for the evolution and maintenance of CRISPR-Cas systems and the contribution of these systems to the ecology and evolution of bacteria, archaea, and the mobile genetic elements that infect them. |
format | Online Article Text |
id | pubmed-7668106 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | National Academy of Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-76681062020-11-27 It is unclear how important CRISPR-Cas systems are for protecting natural populations of bacteria against infections by mobile genetic elements Westra, Edze R. Levin, Bruce R. Proc Natl Acad Sci U S A Perspective Articles on CRISPR commonly open with some variant of the phrase “these short palindromic repeats and their associated endonucleases (Cas) are an adaptive immune system that exists to protect bacteria and archaea from viruses and infections with other mobile genetic elements.” There is an abundance of genomic data consistent with the hypothesis that CRISPR plays this role in natural populations of bacteria and archaea, and experimental demonstrations with a few species of bacteria and their phage and plasmids show that CRISPR-Cas systems can play this role in vitro. Not at all clear are the ubiquity, magnitude, and nature of the contribution of CRISPR-Cas systems to the ecology and evolution of natural populations of microbes and the strength of selection mediated by different types of phage and plasmids to the evolution and maintenance of CRISPR-Cas systems. In this perspective, with the aid of heuristic mathematical–computer simulation models, we explore the a priori conditions under which exposure to lytic and temperate phage and conjugative plasmids will select for and maintain CRISPR-Cas systems in populations of bacteria and archaea. We review the existing literature addressing these ecological and evolutionary questions and highlight the experimental and other evidence needed to fully understand the conditions responsible for the evolution and maintenance of CRISPR-Cas systems and the contribution of these systems to the ecology and evolution of bacteria, archaea, and the mobile genetic elements that infect them. National Academy of Sciences 2020-11-10 2020-10-29 /pmc/articles/PMC7668106/ /pubmed/33122438 http://dx.doi.org/10.1073/pnas.1915966117 Text en Copyright © 2020 the Author(s). Published by PNAS. http://creativecommons.org/licenses/by/4.0/ https://creativecommons.org/licenses/by/4.0/This open access article is distributed under Creative Commons Attribution License 4.0 (CC BY) (http://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Perspective Westra, Edze R. Levin, Bruce R. It is unclear how important CRISPR-Cas systems are for protecting natural populations of bacteria against infections by mobile genetic elements |
title | It is unclear how important CRISPR-Cas systems are for protecting natural populations of bacteria against infections by mobile genetic elements |
title_full | It is unclear how important CRISPR-Cas systems are for protecting natural populations of bacteria against infections by mobile genetic elements |
title_fullStr | It is unclear how important CRISPR-Cas systems are for protecting natural populations of bacteria against infections by mobile genetic elements |
title_full_unstemmed | It is unclear how important CRISPR-Cas systems are for protecting natural populations of bacteria against infections by mobile genetic elements |
title_short | It is unclear how important CRISPR-Cas systems are for protecting natural populations of bacteria against infections by mobile genetic elements |
title_sort | it is unclear how important crispr-cas systems are for protecting natural populations of bacteria against infections by mobile genetic elements |
topic | Perspective |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7668106/ https://www.ncbi.nlm.nih.gov/pubmed/33122438 http://dx.doi.org/10.1073/pnas.1915966117 |
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