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The Zur of Xanthomonas campestris functions as a repressor and an activator of putative zinc homeostasis genes via recognizing two distinct sequences within its target promoters

It has been long considered that zinc homeostasis in bacteria is maintained by export systems and uptake systems, which are separately controlled by their own regulators and the uptake systems are negatively regulated by Zur which binds to an about 30-bp AT-rich sequence known as Zur-box present in...

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Autores principales: Huang, Dong-Liang, Tang, Dong-Jie, Liao, Qing, Li, Heng-Cong, Chen, Qi, He, Yong-Qiang, Feng, Jia-Xun, Jiang, Bo-Le, Lu, Guang-Tao, Chen, Baoshan, Tang, Ji-Liang
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2490734/
https://www.ncbi.nlm.nih.gov/pubmed/18586823
http://dx.doi.org/10.1093/nar/gkn328
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author Huang, Dong-Liang
Tang, Dong-Jie
Liao, Qing
Li, Heng-Cong
Chen, Qi
He, Yong-Qiang
Feng, Jia-Xun
Jiang, Bo-Le
Lu, Guang-Tao
Chen, Baoshan
Tang, Ji-Liang
author_facet Huang, Dong-Liang
Tang, Dong-Jie
Liao, Qing
Li, Heng-Cong
Chen, Qi
He, Yong-Qiang
Feng, Jia-Xun
Jiang, Bo-Le
Lu, Guang-Tao
Chen, Baoshan
Tang, Ji-Liang
author_sort Huang, Dong-Liang
collection PubMed
description It has been long considered that zinc homeostasis in bacteria is maintained by export systems and uptake systems, which are separately controlled by their own regulators and the uptake systems are negatively regulated by Zur which binds to an about 30-bp AT-rich sequence known as Zur-box present in its target promoters to block the entry of RNA polymerase. Here, we demonstrated in vivo and in vitro that in addition to act as a repressor of putative Zn(2+)-uptake systems, the Zur of the bacterial phytopathogen Xanthomonas campestris pathovar campestris (Xcc) acts as an activator of a Zn(2+) efflux pump. The Xcc Zur binds to a similar Zur-box with ∼30-bp AT-rich sequence in the promoters of the genes encoding putative Zn(2+)-uptake systems but a 59-bp GC-rich sequence with a 20-bp inverted repeat overlapping the promoter's −35 to −10 sequence of the gene encoding a Zn(2+)-export system. Mutagenesis of the inverted repeat sequence resulted in abolishment of the in vitro binding and the in vivo and in vitro activation of the export gene's promoter by Zur. These results reveal that the Xcc Zur functions as a repressor and an activator of putative zinc homeostasis genes via recognizing two distinct sequences within its target promoters.
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spelling pubmed-24907342008-08-01 The Zur of Xanthomonas campestris functions as a repressor and an activator of putative zinc homeostasis genes via recognizing two distinct sequences within its target promoters Huang, Dong-Liang Tang, Dong-Jie Liao, Qing Li, Heng-Cong Chen, Qi He, Yong-Qiang Feng, Jia-Xun Jiang, Bo-Le Lu, Guang-Tao Chen, Baoshan Tang, Ji-Liang Nucleic Acids Res Molecular Biology It has been long considered that zinc homeostasis in bacteria is maintained by export systems and uptake systems, which are separately controlled by their own regulators and the uptake systems are negatively regulated by Zur which binds to an about 30-bp AT-rich sequence known as Zur-box present in its target promoters to block the entry of RNA polymerase. Here, we demonstrated in vivo and in vitro that in addition to act as a repressor of putative Zn(2+)-uptake systems, the Zur of the bacterial phytopathogen Xanthomonas campestris pathovar campestris (Xcc) acts as an activator of a Zn(2+) efflux pump. The Xcc Zur binds to a similar Zur-box with ∼30-bp AT-rich sequence in the promoters of the genes encoding putative Zn(2+)-uptake systems but a 59-bp GC-rich sequence with a 20-bp inverted repeat overlapping the promoter's −35 to −10 sequence of the gene encoding a Zn(2+)-export system. Mutagenesis of the inverted repeat sequence resulted in abolishment of the in vitro binding and the in vivo and in vitro activation of the export gene's promoter by Zur. These results reveal that the Xcc Zur functions as a repressor and an activator of putative zinc homeostasis genes via recognizing two distinct sequences within its target promoters. Oxford University Press 2008-08 2008-06-27 /pmc/articles/PMC2490734/ /pubmed/18586823 http://dx.doi.org/10.1093/nar/gkn328 Text en © 2008 The Author(s) http://creativecommons.org/licenses/by-nc/2.0/uk/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Molecular Biology
Huang, Dong-Liang
Tang, Dong-Jie
Liao, Qing
Li, Heng-Cong
Chen, Qi
He, Yong-Qiang
Feng, Jia-Xun
Jiang, Bo-Le
Lu, Guang-Tao
Chen, Baoshan
Tang, Ji-Liang
The Zur of Xanthomonas campestris functions as a repressor and an activator of putative zinc homeostasis genes via recognizing two distinct sequences within its target promoters
title The Zur of Xanthomonas campestris functions as a repressor and an activator of putative zinc homeostasis genes via recognizing two distinct sequences within its target promoters
title_full The Zur of Xanthomonas campestris functions as a repressor and an activator of putative zinc homeostasis genes via recognizing two distinct sequences within its target promoters
title_fullStr The Zur of Xanthomonas campestris functions as a repressor and an activator of putative zinc homeostasis genes via recognizing two distinct sequences within its target promoters
title_full_unstemmed The Zur of Xanthomonas campestris functions as a repressor and an activator of putative zinc homeostasis genes via recognizing two distinct sequences within its target promoters
title_short The Zur of Xanthomonas campestris functions as a repressor and an activator of putative zinc homeostasis genes via recognizing two distinct sequences within its target promoters
title_sort zur of xanthomonas campestris functions as a repressor and an activator of putative zinc homeostasis genes via recognizing two distinct sequences within its target promoters
topic Molecular Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2490734/
https://www.ncbi.nlm.nih.gov/pubmed/18586823
http://dx.doi.org/10.1093/nar/gkn328
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