A cyclic di-GMP-binding adaptor protein interacts with a N5-glutamine methyltransferase to regulate the pathogenesis in Xanthomonas citri subsp. citri

The second messenger cyclic diguanylate monophosphate (c-di-GMP) regulates a wide range of bacterial behaviours through diverse mechanisms and binding receptors. Single-domain PilZ proteins, the most widespread and abundant known c-di-GMP receptors in bacteria, act as trans-acting adaptor proteins t...

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Main Authors: Shi, Yu, Cheng, Tianfang, Cheang, Qing Wei, Zhao, Xiaoyan, Xu, Zeling, Liang, Zhao-Xun, Xu, Linghui, Wang, Junxia
Other Authors: School of Biological Sciences
Format: Article
Language:English
Published: 2024
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Online Access:https://hdl.handle.net/10356/181632
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Institution: Nanyang Technological University
Language: English
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spelling sg-ntu-dr.10356-1816322024-12-16T15:32:29Z A cyclic di-GMP-binding adaptor protein interacts with a N5-glutamine methyltransferase to regulate the pathogenesis in Xanthomonas citri subsp. citri Shi, Yu Cheng, Tianfang Cheang, Qing Wei Zhao, Xiaoyan Xu, Zeling Liang, Zhao-Xun Xu, Linghui Wang, Junxia School of Biological Sciences Medicine, Health and Life Sciences Stress tolerance Virulence The second messenger cyclic diguanylate monophosphate (c-di-GMP) regulates a wide range of bacterial behaviours through diverse mechanisms and binding receptors. Single-domain PilZ proteins, the most widespread and abundant known c-di-GMP receptors in bacteria, act as trans-acting adaptor proteins that enable c-di-GMP to control signalling pathways with high specificity. This study identifies a single-domain PilZ protein, XAC3402 (renamed N5MapZ), from the phytopathogen Xanthomonas citri subsp. citri (Xcc), which modulates Xcc virulence by directly interacting with the methyltransferase HemK. Through yeast two-hybrid, co-immunoprecipitation and immunofluorescent staining, we demonstrated that N5MapZ and HemK interact directly under both in vitro and in vivo conditions, with the strength of the protein-protein interaction decreasing at high c-di-GMP concentrations. This finding distinguishes N5MapZ from other characterized single-domain PilZ proteins, as it was previously known that c-di-GMP enhances the interaction between those single-domain PilZs and their protein partners. This observation is further supported by the fact that the c-di-GMP binding-defective mutant N5MapZR10A can interact with HemK to inhibit the methylation of the class 1 translation termination release factor PrfA. Additionally, we found that HemK plays an important role in Xcc pathogenesis, as the deletion of hemK leads to extensive phenotypic changes, including reduced virulence in citrus plants, decreased motility, production of extracellular enzymes and stress tolerance. Gene expression analysis has revealed that c-di-GMP and the HemK-mediated pathway regulate the expression of multiple virulence effector proteins, uncovering a novel regulatory mechanism through which c-di-GMP regulates Xcc virulence by mediating PrfA methylation via the single-domain PilZ adaptor protein N5MapZ. Published version This work was supported by the Natural Science Foundation of Guangdong Province, China (2021A1515010761 and 2022A1515010869) and the Basic and Applied Basic Research Project of Guangzhou Basic Research Program, China (202201010058). 2024-12-11T02:19:12Z 2024-12-11T02:19:12Z 2024 Journal Article Shi, Y., Cheng, T., Cheang, Q. W., Zhao, X., Xu, Z., Liang, Z., Xu, L. & Wang, J. (2024). A cyclic di-GMP-binding adaptor protein interacts with a N5-glutamine methyltransferase to regulate the pathogenesis in Xanthomonas citri subsp. citri. Molecular Plant Pathology, 25(7), e13496-. https://dx.doi.org/10.1111/mpp.13496 1464-6722 https://hdl.handle.net/10356/181632 10.1111/mpp.13496 39011828 2-s2.0-85198702253 7 25 e13496 en Molecular Plant Pathology © 2024 The Author(s). 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 Creative Commons Attribution-NonCommercial License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. application/pdf
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic Medicine, Health and Life Sciences
Stress tolerance
Virulence
spellingShingle Medicine, Health and Life Sciences
Stress tolerance
Virulence
Shi, Yu
Cheng, Tianfang
Cheang, Qing Wei
Zhao, Xiaoyan
Xu, Zeling
Liang, Zhao-Xun
Xu, Linghui
Wang, Junxia
A cyclic di-GMP-binding adaptor protein interacts with a N5-glutamine methyltransferase to regulate the pathogenesis in Xanthomonas citri subsp. citri
description The second messenger cyclic diguanylate monophosphate (c-di-GMP) regulates a wide range of bacterial behaviours through diverse mechanisms and binding receptors. Single-domain PilZ proteins, the most widespread and abundant known c-di-GMP receptors in bacteria, act as trans-acting adaptor proteins that enable c-di-GMP to control signalling pathways with high specificity. This study identifies a single-domain PilZ protein, XAC3402 (renamed N5MapZ), from the phytopathogen Xanthomonas citri subsp. citri (Xcc), which modulates Xcc virulence by directly interacting with the methyltransferase HemK. Through yeast two-hybrid, co-immunoprecipitation and immunofluorescent staining, we demonstrated that N5MapZ and HemK interact directly under both in vitro and in vivo conditions, with the strength of the protein-protein interaction decreasing at high c-di-GMP concentrations. This finding distinguishes N5MapZ from other characterized single-domain PilZ proteins, as it was previously known that c-di-GMP enhances the interaction between those single-domain PilZs and their protein partners. This observation is further supported by the fact that the c-di-GMP binding-defective mutant N5MapZR10A can interact with HemK to inhibit the methylation of the class 1 translation termination release factor PrfA. Additionally, we found that HemK plays an important role in Xcc pathogenesis, as the deletion of hemK leads to extensive phenotypic changes, including reduced virulence in citrus plants, decreased motility, production of extracellular enzymes and stress tolerance. Gene expression analysis has revealed that c-di-GMP and the HemK-mediated pathway regulate the expression of multiple virulence effector proteins, uncovering a novel regulatory mechanism through which c-di-GMP regulates Xcc virulence by mediating PrfA methylation via the single-domain PilZ adaptor protein N5MapZ.
author2 School of Biological Sciences
author_facet School of Biological Sciences
Shi, Yu
Cheng, Tianfang
Cheang, Qing Wei
Zhao, Xiaoyan
Xu, Zeling
Liang, Zhao-Xun
Xu, Linghui
Wang, Junxia
format Article
author Shi, Yu
Cheng, Tianfang
Cheang, Qing Wei
Zhao, Xiaoyan
Xu, Zeling
Liang, Zhao-Xun
Xu, Linghui
Wang, Junxia
author_sort Shi, Yu
title A cyclic di-GMP-binding adaptor protein interacts with a N5-glutamine methyltransferase to regulate the pathogenesis in Xanthomonas citri subsp. citri
title_short A cyclic di-GMP-binding adaptor protein interacts with a N5-glutamine methyltransferase to regulate the pathogenesis in Xanthomonas citri subsp. citri
title_full A cyclic di-GMP-binding adaptor protein interacts with a N5-glutamine methyltransferase to regulate the pathogenesis in Xanthomonas citri subsp. citri
title_fullStr A cyclic di-GMP-binding adaptor protein interacts with a N5-glutamine methyltransferase to regulate the pathogenesis in Xanthomonas citri subsp. citri
title_full_unstemmed A cyclic di-GMP-binding adaptor protein interacts with a N5-glutamine methyltransferase to regulate the pathogenesis in Xanthomonas citri subsp. citri
title_sort cyclic di-gmp-binding adaptor protein interacts with a n5-glutamine methyltransferase to regulate the pathogenesis in xanthomonas citri subsp. citri
publishDate 2024
url https://hdl.handle.net/10356/181632
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