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Xanthomonas campestris sensor kinase HpaS co‐opts the orphan response regulator VemR to form a branched two‐component system that regulates motility
Xanthomonas campestris pv. campestris (Xcc) controls virulence and plant infection mechanisms via the activity of the sensor kinase and response regulator pair HpaS/hypersensitive response and pathogenicity G (HrpG). Detailed analysis of the regulatory role of HpaS has suggested the occurrence of fu...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7036368/ https://www.ncbi.nlm.nih.gov/pubmed/31919999 http://dx.doi.org/10.1111/mpp.12901 |
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author | Li, Rui‐Fang Wang, Xin‐Xin Wu, Liu Huang, Li Qin, Qi‐Jian Yao, Jia‐Li Lu, Guang‐Tao Tang, Ji‐Liang |
author_facet | Li, Rui‐Fang Wang, Xin‐Xin Wu, Liu Huang, Li Qin, Qi‐Jian Yao, Jia‐Li Lu, Guang‐Tao Tang, Ji‐Liang |
author_sort | Li, Rui‐Fang |
collection | PubMed |
description | Xanthomonas campestris pv. campestris (Xcc) controls virulence and plant infection mechanisms via the activity of the sensor kinase and response regulator pair HpaS/hypersensitive response and pathogenicity G (HrpG). Detailed analysis of the regulatory role of HpaS has suggested the occurrence of further regulators besides HrpG. Here we used in vitro and in vivo approaches to identify the orphan response regulator VemR as another partner of HpaS and to characterize relevant interactions between components of this signalling system. Bacterial two‐hybrid and protein pull‐down assays revealed that HpaS physically interacts with VemR. Phos‐tag SDS‐PAGE analysis showed that mutation in hpaS reduced markedly the phosphorylation of VemR in vivo. Mutation analysis reveals that HpaS and VemR contribute to the regulation of motility and this relationship appears to be epistatic. Additionally, we show that VemR control of Xcc motility is due in part to its ability to interact and bind to the flagellum rotor protein FliM. Taken together, the findings describe the unrecognized regulatory role of sensor kinase HpaS and orphan response regulator VemR in the control of motility in Xcc and contribute to the understanding of the complex regulatory mechanisms used by Xcc during plant infection. |
format | Online Article Text |
id | pubmed-7036368 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-70363682020-02-26 Xanthomonas campestris sensor kinase HpaS co‐opts the orphan response regulator VemR to form a branched two‐component system that regulates motility Li, Rui‐Fang Wang, Xin‐Xin Wu, Liu Huang, Li Qin, Qi‐Jian Yao, Jia‐Li Lu, Guang‐Tao Tang, Ji‐Liang Mol Plant Pathol Original Articles Xanthomonas campestris pv. campestris (Xcc) controls virulence and plant infection mechanisms via the activity of the sensor kinase and response regulator pair HpaS/hypersensitive response and pathogenicity G (HrpG). Detailed analysis of the regulatory role of HpaS has suggested the occurrence of further regulators besides HrpG. Here we used in vitro and in vivo approaches to identify the orphan response regulator VemR as another partner of HpaS and to characterize relevant interactions between components of this signalling system. Bacterial two‐hybrid and protein pull‐down assays revealed that HpaS physically interacts with VemR. Phos‐tag SDS‐PAGE analysis showed that mutation in hpaS reduced markedly the phosphorylation of VemR in vivo. Mutation analysis reveals that HpaS and VemR contribute to the regulation of motility and this relationship appears to be epistatic. Additionally, we show that VemR control of Xcc motility is due in part to its ability to interact and bind to the flagellum rotor protein FliM. Taken together, the findings describe the unrecognized regulatory role of sensor kinase HpaS and orphan response regulator VemR in the control of motility in Xcc and contribute to the understanding of the complex regulatory mechanisms used by Xcc during plant infection. John Wiley and Sons Inc. 2020-01-09 /pmc/articles/PMC7036368/ /pubmed/31919999 http://dx.doi.org/10.1111/mpp.12901 Text en © 2020 College of Life Science and Technology, Guangxi University. Molecular Plant Pathology published by British Society for Plant Pathology and John Wiley & Sons Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Li, Rui‐Fang Wang, Xin‐Xin Wu, Liu Huang, Li Qin, Qi‐Jian Yao, Jia‐Li Lu, Guang‐Tao Tang, Ji‐Liang Xanthomonas campestris sensor kinase HpaS co‐opts the orphan response regulator VemR to form a branched two‐component system that regulates motility |
title |
Xanthomonas campestris sensor kinase HpaS co‐opts the orphan response regulator VemR to form a branched two‐component system that regulates motility |
title_full |
Xanthomonas campestris sensor kinase HpaS co‐opts the orphan response regulator VemR to form a branched two‐component system that regulates motility |
title_fullStr |
Xanthomonas campestris sensor kinase HpaS co‐opts the orphan response regulator VemR to form a branched two‐component system that regulates motility |
title_full_unstemmed |
Xanthomonas campestris sensor kinase HpaS co‐opts the orphan response regulator VemR to form a branched two‐component system that regulates motility |
title_short |
Xanthomonas campestris sensor kinase HpaS co‐opts the orphan response regulator VemR to form a branched two‐component system that regulates motility |
title_sort | xanthomonas campestris sensor kinase hpas co‐opts the orphan response regulator vemr to form a branched two‐component system that regulates motility |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7036368/ https://www.ncbi.nlm.nih.gov/pubmed/31919999 http://dx.doi.org/10.1111/mpp.12901 |
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