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The PAS domain‐containing histidine kinase RpfS is a second sensor for the diffusible signal factor of Xanthomonas campestris

A cell–cell signalling system mediated by the fatty acid signal DSF controls the virulence of Xanthomonas campestris pv. campestris (Xcc) to plants. The synthesis and recognition of the DSF signal depends upon different Rpf proteins. DSF signal generation requires RpfF whereas signal perception and...

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Autores principales: An, Shi‐Qi, Allan, John H., McCarthy, Yvonne, Febrer, Melanie, Dow, J. Maxwell, Ryan, Robert P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Scientific Publications 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4159695/
https://www.ncbi.nlm.nih.gov/pubmed/24617591
http://dx.doi.org/10.1111/mmi.12577
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author An, Shi‐Qi
Allan, John H.
McCarthy, Yvonne
Febrer, Melanie
Dow, J. Maxwell
Ryan, Robert P.
author_facet An, Shi‐Qi
Allan, John H.
McCarthy, Yvonne
Febrer, Melanie
Dow, J. Maxwell
Ryan, Robert P.
author_sort An, Shi‐Qi
collection PubMed
description A cell–cell signalling system mediated by the fatty acid signal DSF controls the virulence of Xanthomonas campestris pv. campestris (Xcc) to plants. The synthesis and recognition of the DSF signal depends upon different Rpf proteins. DSF signal generation requires RpfF whereas signal perception and transduction depends upon the sensor RpfC and regulator RpfG. Detailed analyses of the regulatory roles of different Rpf proteins have suggested the occurrence of further sensors for DSF. Here we have used a mutagenesis approach coupled with high‐resolution transcriptional analysis to identify XC_2579 (RpfS) as a second sensor for DSF in Xcc. RpfS is a complex sensor kinase predicted to have multiple Per/Arnt/Sim (PAS) domains, a histidine kinase domain and a C‐terminal receiver (REC) domain. Isothermal calorimetry showed that DSF bound to the isolated N‐terminal PAS domain with a K(d) of 1.4 μM. RpfS controlled expression of a sub‐set of genes distinct from those controlled by RpfC to include genes involved in type IV secretion and chemotaxis. Mutation of XC_2579 was associated with a reduction in virulence of Xcc to Chinese Radish when assayed by leaf spraying but not by leaf inoculation, suggesting a role for RpfS‐controlled factors in the epiphytic phase of the disease cycle.
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spelling pubmed-41596952014-09-22 The PAS domain‐containing histidine kinase RpfS is a second sensor for the diffusible signal factor of Xanthomonas campestris An, Shi‐Qi Allan, John H. McCarthy, Yvonne Febrer, Melanie Dow, J. Maxwell Ryan, Robert P. Mol Microbiol Research Articles A cell–cell signalling system mediated by the fatty acid signal DSF controls the virulence of Xanthomonas campestris pv. campestris (Xcc) to plants. The synthesis and recognition of the DSF signal depends upon different Rpf proteins. DSF signal generation requires RpfF whereas signal perception and transduction depends upon the sensor RpfC and regulator RpfG. Detailed analyses of the regulatory roles of different Rpf proteins have suggested the occurrence of further sensors for DSF. Here we have used a mutagenesis approach coupled with high‐resolution transcriptional analysis to identify XC_2579 (RpfS) as a second sensor for DSF in Xcc. RpfS is a complex sensor kinase predicted to have multiple Per/Arnt/Sim (PAS) domains, a histidine kinase domain and a C‐terminal receiver (REC) domain. Isothermal calorimetry showed that DSF bound to the isolated N‐terminal PAS domain with a K(d) of 1.4 μM. RpfS controlled expression of a sub‐set of genes distinct from those controlled by RpfC to include genes involved in type IV secretion and chemotaxis. Mutation of XC_2579 was associated with a reduction in virulence of Xcc to Chinese Radish when assayed by leaf spraying but not by leaf inoculation, suggesting a role for RpfS‐controlled factors in the epiphytic phase of the disease cycle. Blackwell Scientific Publications 2014-04-02 2014-05 /pmc/articles/PMC4159695/ /pubmed/24617591 http://dx.doi.org/10.1111/mmi.12577 Text en © 2014 The Authors. Molecular Microbiology published by John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/3.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Research Articles
An, Shi‐Qi
Allan, John H.
McCarthy, Yvonne
Febrer, Melanie
Dow, J. Maxwell
Ryan, Robert P.
The PAS domain‐containing histidine kinase RpfS is a second sensor for the diffusible signal factor of Xanthomonas campestris
title The PAS domain‐containing histidine kinase RpfS is a second sensor for the diffusible signal factor of Xanthomonas campestris
title_full The PAS domain‐containing histidine kinase RpfS is a second sensor for the diffusible signal factor of Xanthomonas campestris
title_fullStr The PAS domain‐containing histidine kinase RpfS is a second sensor for the diffusible signal factor of Xanthomonas campestris
title_full_unstemmed The PAS domain‐containing histidine kinase RpfS is a second sensor for the diffusible signal factor of Xanthomonas campestris
title_short The PAS domain‐containing histidine kinase RpfS is a second sensor for the diffusible signal factor of Xanthomonas campestris
title_sort pas domain‐containing histidine kinase rpfs is a second sensor for the diffusible signal factor of xanthomonas campestris
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4159695/
https://www.ncbi.nlm.nih.gov/pubmed/24617591
http://dx.doi.org/10.1111/mmi.12577
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