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The Cyclic Oligoadenylate Signaling Pathway of Type III CRISPR-Cas Systems
Type III CRISPR-Cas systems, which are widespread in both bacteria and archaea, provide immunity against DNA viruses and plasmids in a transcription-dependent manner. Since an unprecedented cyclic oligoadenylate (cOA) signaling pathway was discovered in type III systems in 2017, the cOA signaling ha...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7854544/ https://www.ncbi.nlm.nih.gov/pubmed/33552016 http://dx.doi.org/10.3389/fmicb.2020.602789 |
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author | Huang, Fengtao Zhu, Bin |
author_facet | Huang, Fengtao Zhu, Bin |
author_sort | Huang, Fengtao |
collection | PubMed |
description | Type III CRISPR-Cas systems, which are widespread in both bacteria and archaea, provide immunity against DNA viruses and plasmids in a transcription-dependent manner. Since an unprecedented cyclic oligoadenylate (cOA) signaling pathway was discovered in type III systems in 2017, the cOA signaling has been extensively studied in recent 3 years, which has expanded our understanding of type III systems immune defense and also its counteraction by viruses. In this review, we summarized recent advances in cOA synthesis, cOA-activated effector protein, cOA signaling-mediated immunoprotection, and cOA signaling inhibition, and highlighted the crosstalk between cOA signaling and other cyclic oligonucleotide-mediated immunity discovered very recently. |
format | Online Article Text |
id | pubmed-7854544 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-78545442021-02-04 The Cyclic Oligoadenylate Signaling Pathway of Type III CRISPR-Cas Systems Huang, Fengtao Zhu, Bin Front Microbiol Microbiology Type III CRISPR-Cas systems, which are widespread in both bacteria and archaea, provide immunity against DNA viruses and plasmids in a transcription-dependent manner. Since an unprecedented cyclic oligoadenylate (cOA) signaling pathway was discovered in type III systems in 2017, the cOA signaling has been extensively studied in recent 3 years, which has expanded our understanding of type III systems immune defense and also its counteraction by viruses. In this review, we summarized recent advances in cOA synthesis, cOA-activated effector protein, cOA signaling-mediated immunoprotection, and cOA signaling inhibition, and highlighted the crosstalk between cOA signaling and other cyclic oligonucleotide-mediated immunity discovered very recently. Frontiers Media S.A. 2021-01-20 /pmc/articles/PMC7854544/ /pubmed/33552016 http://dx.doi.org/10.3389/fmicb.2020.602789 Text en Copyright © 2021 Huang and Zhu. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Microbiology Huang, Fengtao Zhu, Bin The Cyclic Oligoadenylate Signaling Pathway of Type III CRISPR-Cas Systems |
title | The Cyclic Oligoadenylate Signaling Pathway of Type III CRISPR-Cas Systems |
title_full | The Cyclic Oligoadenylate Signaling Pathway of Type III CRISPR-Cas Systems |
title_fullStr | The Cyclic Oligoadenylate Signaling Pathway of Type III CRISPR-Cas Systems |
title_full_unstemmed | The Cyclic Oligoadenylate Signaling Pathway of Type III CRISPR-Cas Systems |
title_short | The Cyclic Oligoadenylate Signaling Pathway of Type III CRISPR-Cas Systems |
title_sort | cyclic oligoadenylate signaling pathway of type iii crispr-cas systems |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7854544/ https://www.ncbi.nlm.nih.gov/pubmed/33552016 http://dx.doi.org/10.3389/fmicb.2020.602789 |
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