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A Zur-mediated transcriptional regulation of the zinc export system in Pseudomonas aeruginosa
The control of cellular zinc (Zn) concentrations by dedicated import and export systems is essential for the survival and virulence of Pseudomonas aeruginosa. The transcription of its many Zn transporters is therefore tightly regulated by a known set of transcription factors involved in either the i...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9827704/ https://www.ncbi.nlm.nih.gov/pubmed/36617571 http://dx.doi.org/10.1186/s12866-022-02750-4 |
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author | Ducret, Verena Gonzalez, Diego Leoni, Sara Valentini, Martina Perron, Karl |
author_facet | Ducret, Verena Gonzalez, Diego Leoni, Sara Valentini, Martina Perron, Karl |
author_sort | Ducret, Verena |
collection | PubMed |
description | The control of cellular zinc (Zn) concentrations by dedicated import and export systems is essential for the survival and virulence of Pseudomonas aeruginosa. The transcription of its many Zn transporters is therefore tightly regulated by a known set of transcription factors involved in either the import or the export of Zn. In this work, we show that the Zur protein, a well-known repressor of Zn import, plays a dual role and functions in both import and export processes. In a situation of Zn excess, Zur represses Zn entry, but also activates the transcription of czcR, a positive regulator of the Zn export system. To achieve this, Zur binds at two sites, located by DNA footprinting in the region downstream the czcR transcription start site. In agreement with this regulation, a delay in induction of the efflux system is observed in the absence of Zur and Zn resistance is reduced. The discovery of this regulation highlights a new role of Zur as global regulator of Zn homeostasis in P. aeruginosa disclosing an important link between Zur and zinc export. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12866-022-02750-4. |
format | Online Article Text |
id | pubmed-9827704 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-98277042023-01-10 A Zur-mediated transcriptional regulation of the zinc export system in Pseudomonas aeruginosa Ducret, Verena Gonzalez, Diego Leoni, Sara Valentini, Martina Perron, Karl BMC Microbiol Research The control of cellular zinc (Zn) concentrations by dedicated import and export systems is essential for the survival and virulence of Pseudomonas aeruginosa. The transcription of its many Zn transporters is therefore tightly regulated by a known set of transcription factors involved in either the import or the export of Zn. In this work, we show that the Zur protein, a well-known repressor of Zn import, plays a dual role and functions in both import and export processes. In a situation of Zn excess, Zur represses Zn entry, but also activates the transcription of czcR, a positive regulator of the Zn export system. To achieve this, Zur binds at two sites, located by DNA footprinting in the region downstream the czcR transcription start site. In agreement with this regulation, a delay in induction of the efflux system is observed in the absence of Zur and Zn resistance is reduced. The discovery of this regulation highlights a new role of Zur as global regulator of Zn homeostasis in P. aeruginosa disclosing an important link between Zur and zinc export. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12866-022-02750-4. BioMed Central 2023-01-09 /pmc/articles/PMC9827704/ /pubmed/36617571 http://dx.doi.org/10.1186/s12866-022-02750-4 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Ducret, Verena Gonzalez, Diego Leoni, Sara Valentini, Martina Perron, Karl A Zur-mediated transcriptional regulation of the zinc export system in Pseudomonas aeruginosa |
title | A Zur-mediated transcriptional regulation of the zinc export system in Pseudomonas aeruginosa |
title_full | A Zur-mediated transcriptional regulation of the zinc export system in Pseudomonas aeruginosa |
title_fullStr | A Zur-mediated transcriptional regulation of the zinc export system in Pseudomonas aeruginosa |
title_full_unstemmed | A Zur-mediated transcriptional regulation of the zinc export system in Pseudomonas aeruginosa |
title_short | A Zur-mediated transcriptional regulation of the zinc export system in Pseudomonas aeruginosa |
title_sort | zur-mediated transcriptional regulation of the zinc export system in pseudomonas aeruginosa |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9827704/ https://www.ncbi.nlm.nih.gov/pubmed/36617571 http://dx.doi.org/10.1186/s12866-022-02750-4 |
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