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Structural insights into the inactivation of CRISPR-Cas systems by diverse anti-CRISPR proteins

A molecular arms race is progressively being unveiled between prokaryotes and viruses. Prokaryotes utilize CRISPR-mediated adaptive immune systems to kill the invading phages and mobile genetic elements, and in turn, the viruses evolve diverse anti-CRISPR proteins to fight back. The structures of se...

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Detalles Bibliográficos
Autores principales: Zhu, Yuwei, Zhang, Fan, Huang, Zhiwei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5859409/
https://www.ncbi.nlm.nih.gov/pubmed/29554913
http://dx.doi.org/10.1186/s12915-018-0504-9
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author Zhu, Yuwei
Zhang, Fan
Huang, Zhiwei
author_facet Zhu, Yuwei
Zhang, Fan
Huang, Zhiwei
author_sort Zhu, Yuwei
collection PubMed
description A molecular arms race is progressively being unveiled between prokaryotes and viruses. Prokaryotes utilize CRISPR-mediated adaptive immune systems to kill the invading phages and mobile genetic elements, and in turn, the viruses evolve diverse anti-CRISPR proteins to fight back. The structures of several anti-CRISPR proteins have now been reported, and here we discuss their structural features, with a particular emphasis on topology, to discover their similarities and differences. We summarize the CRISPR-Cas inhibition mechanisms of these anti-CRISPR proteins in their structural context. Considering anti-CRISPRs in this way will provide important clues for studying their origin and evolution.
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spelling pubmed-58594092018-03-20 Structural insights into the inactivation of CRISPR-Cas systems by diverse anti-CRISPR proteins Zhu, Yuwei Zhang, Fan Huang, Zhiwei BMC Biol Review A molecular arms race is progressively being unveiled between prokaryotes and viruses. Prokaryotes utilize CRISPR-mediated adaptive immune systems to kill the invading phages and mobile genetic elements, and in turn, the viruses evolve diverse anti-CRISPR proteins to fight back. The structures of several anti-CRISPR proteins have now been reported, and here we discuss their structural features, with a particular emphasis on topology, to discover their similarities and differences. We summarize the CRISPR-Cas inhibition mechanisms of these anti-CRISPR proteins in their structural context. Considering anti-CRISPRs in this way will provide important clues for studying their origin and evolution. BioMed Central 2018-03-19 /pmc/articles/PMC5859409/ /pubmed/29554913 http://dx.doi.org/10.1186/s12915-018-0504-9 Text en © Zhu et al. 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Review
Zhu, Yuwei
Zhang, Fan
Huang, Zhiwei
Structural insights into the inactivation of CRISPR-Cas systems by diverse anti-CRISPR proteins
title Structural insights into the inactivation of CRISPR-Cas systems by diverse anti-CRISPR proteins
title_full Structural insights into the inactivation of CRISPR-Cas systems by diverse anti-CRISPR proteins
title_fullStr Structural insights into the inactivation of CRISPR-Cas systems by diverse anti-CRISPR proteins
title_full_unstemmed Structural insights into the inactivation of CRISPR-Cas systems by diverse anti-CRISPR proteins
title_short Structural insights into the inactivation of CRISPR-Cas systems by diverse anti-CRISPR proteins
title_sort structural insights into the inactivation of crispr-cas systems by diverse anti-crispr proteins
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5859409/
https://www.ncbi.nlm.nih.gov/pubmed/29554913
http://dx.doi.org/10.1186/s12915-018-0504-9
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