Cargando…
A histidine kinase and a response regulator provide phage resistance to Marinomonas mediterranea via CRISPR-Cas regulation
CRISPR-Cas systems are used by many prokaryotes to defend against invading genetic elements. In many cases, more than one CRISPR-Cas system co-exist in the same cell. Marinomonas mediterranea MMB-1 possesses two CRISPR-Cas systems, of type I–F and III-B respectively, which collaborate in phage resis...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8523701/ https://www.ncbi.nlm.nih.gov/pubmed/34663886 http://dx.doi.org/10.1038/s41598-021-99740-9 |
_version_ | 1784585346334326784 |
---|---|
author | Lucas-Elío, Patricia Molina-Quintero, Luisa Raquel Xu, Hengyi Sánchez-Amat, Antonio |
author_facet | Lucas-Elío, Patricia Molina-Quintero, Luisa Raquel Xu, Hengyi Sánchez-Amat, Antonio |
author_sort | Lucas-Elío, Patricia |
collection | PubMed |
description | CRISPR-Cas systems are used by many prokaryotes to defend against invading genetic elements. In many cases, more than one CRISPR-Cas system co-exist in the same cell. Marinomonas mediterranea MMB-1 possesses two CRISPR-Cas systems, of type I–F and III-B respectively, which collaborate in phage resistance raising questions on how their expression is regulated. This study shows that the expression of both systems is controlled by the histidine kinase PpoS and a response regulator, PpoR, identified and cloned in this study. These proteins show similarity to the global regulators BarA/UvrY. In addition, homologues to the sRNAs CsrB and CsrC and the gene coding for the post-transcriptional repressor CsrA have been also identified indicating the conservation of the elements of the BarA/UvrY regulatory cascade in M. mediterranea. RNA-Seq analyses have revealed that all these genetics elements are regulated by PpoS/R supporting their participation in the regulatory cascade. The regulation by PpoS and PpoR of the CRISPR-Cas systems plays a role in phage defense since mutants in these proteins show an increase in phage sensitivity. |
format | Online Article Text |
id | pubmed-8523701 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-85237012021-10-20 A histidine kinase and a response regulator provide phage resistance to Marinomonas mediterranea via CRISPR-Cas regulation Lucas-Elío, Patricia Molina-Quintero, Luisa Raquel Xu, Hengyi Sánchez-Amat, Antonio Sci Rep Article CRISPR-Cas systems are used by many prokaryotes to defend against invading genetic elements. In many cases, more than one CRISPR-Cas system co-exist in the same cell. Marinomonas mediterranea MMB-1 possesses two CRISPR-Cas systems, of type I–F and III-B respectively, which collaborate in phage resistance raising questions on how their expression is regulated. This study shows that the expression of both systems is controlled by the histidine kinase PpoS and a response regulator, PpoR, identified and cloned in this study. These proteins show similarity to the global regulators BarA/UvrY. In addition, homologues to the sRNAs CsrB and CsrC and the gene coding for the post-transcriptional repressor CsrA have been also identified indicating the conservation of the elements of the BarA/UvrY regulatory cascade in M. mediterranea. RNA-Seq analyses have revealed that all these genetics elements are regulated by PpoS/R supporting their participation in the regulatory cascade. The regulation by PpoS and PpoR of the CRISPR-Cas systems plays a role in phage defense since mutants in these proteins show an increase in phage sensitivity. Nature Publishing Group UK 2021-10-18 /pmc/articles/PMC8523701/ /pubmed/34663886 http://dx.doi.org/10.1038/s41598-021-99740-9 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Lucas-Elío, Patricia Molina-Quintero, Luisa Raquel Xu, Hengyi Sánchez-Amat, Antonio A histidine kinase and a response regulator provide phage resistance to Marinomonas mediterranea via CRISPR-Cas regulation |
title | A histidine kinase and a response regulator provide phage resistance to Marinomonas mediterranea via CRISPR-Cas regulation |
title_full | A histidine kinase and a response regulator provide phage resistance to Marinomonas mediterranea via CRISPR-Cas regulation |
title_fullStr | A histidine kinase and a response regulator provide phage resistance to Marinomonas mediterranea via CRISPR-Cas regulation |
title_full_unstemmed | A histidine kinase and a response regulator provide phage resistance to Marinomonas mediterranea via CRISPR-Cas regulation |
title_short | A histidine kinase and a response regulator provide phage resistance to Marinomonas mediterranea via CRISPR-Cas regulation |
title_sort | histidine kinase and a response regulator provide phage resistance to marinomonas mediterranea via crispr-cas regulation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8523701/ https://www.ncbi.nlm.nih.gov/pubmed/34663886 http://dx.doi.org/10.1038/s41598-021-99740-9 |
work_keys_str_mv | AT lucaseliopatricia ahistidinekinaseandaresponseregulatorprovidephageresistancetomarinomonasmediterraneaviacrisprcasregulation AT molinaquinteroluisaraquel ahistidinekinaseandaresponseregulatorprovidephageresistancetomarinomonasmediterraneaviacrisprcasregulation AT xuhengyi ahistidinekinaseandaresponseregulatorprovidephageresistancetomarinomonasmediterraneaviacrisprcasregulation AT sanchezamatantonio ahistidinekinaseandaresponseregulatorprovidephageresistancetomarinomonasmediterraneaviacrisprcasregulation AT lucaseliopatricia histidinekinaseandaresponseregulatorprovidephageresistancetomarinomonasmediterraneaviacrisprcasregulation AT molinaquinteroluisaraquel histidinekinaseandaresponseregulatorprovidephageresistancetomarinomonasmediterraneaviacrisprcasregulation AT xuhengyi histidinekinaseandaresponseregulatorprovidephageresistancetomarinomonasmediterraneaviacrisprcasregulation AT sanchezamatantonio histidinekinaseandaresponseregulatorprovidephageresistancetomarinomonasmediterraneaviacrisprcasregulation |