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Chloroplast clustering around the nucleus induced by OMP24 overexpression unexpectedly promoted PSTVd infection in Nicotiana benthamiana
Chloroplast clustering around the nucleus is a well‐known mechanism that occurs in response to various biotic and abiotic stresses and is believed to be a mechanism of defence against pathogens in plants. This phenomenon is accompanied by increased production of reactive oxygen species (ROS), which...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10632781/ https://www.ncbi.nlm.nih.gov/pubmed/37695572 http://dx.doi.org/10.1111/mpp.13385 |
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author | Han, Kelei Jia, Zhaoxing Zhang, Yuhong Zhou, Huijie Bu, Shan Chen, Jianping Yan, Dankan Qi, Rende Yan, Fei Wu, Jian |
author_facet | Han, Kelei Jia, Zhaoxing Zhang, Yuhong Zhou, Huijie Bu, Shan Chen, Jianping Yan, Dankan Qi, Rende Yan, Fei Wu, Jian |
author_sort | Han, Kelei |
collection | PubMed |
description | Chloroplast clustering around the nucleus is a well‐known mechanism that occurs in response to various biotic and abiotic stresses and is believed to be a mechanism of defence against pathogens in plants. This phenomenon is accompanied by increased production of reactive oxygen species (ROS), which can help to destroy invading pathogens. However, the function of chloroplast clustering during viroid infection is unclear. Here, we report that, although the infection by potato spindle tuber viroid (PSTVd) failed to induce chloroplast clustering, chloroplast clustering caused by the overexpression of the Nicotiana benthamiana chloroplast outer membrane protein 24 (NbOMP24) promoted the infection by PSTVd, a viroid pathogen, in N. benthamiana. Interestingly, H(2)O(2) treatment, which caused increased ROS accumulation, showed no significant effects on PSTVd infection. Moreover, NbOMP24 protein showed no direct interaction with PSTVd. We propose that perinuclear chloroplast clustering induced by NbOMP24 provides a favourable environment for PSTVd infection. These findings highlight the complexity of chloroplast clustering‐mediated plant–pathogen interactions and the need for further research to fully understand these mechanisms. |
format | Online Article Text |
id | pubmed-10632781 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-106327812023-11-15 Chloroplast clustering around the nucleus induced by OMP24 overexpression unexpectedly promoted PSTVd infection in Nicotiana benthamiana Han, Kelei Jia, Zhaoxing Zhang, Yuhong Zhou, Huijie Bu, Shan Chen, Jianping Yan, Dankan Qi, Rende Yan, Fei Wu, Jian Mol Plant Pathol Short Communication Chloroplast clustering around the nucleus is a well‐known mechanism that occurs in response to various biotic and abiotic stresses and is believed to be a mechanism of defence against pathogens in plants. This phenomenon is accompanied by increased production of reactive oxygen species (ROS), which can help to destroy invading pathogens. However, the function of chloroplast clustering during viroid infection is unclear. Here, we report that, although the infection by potato spindle tuber viroid (PSTVd) failed to induce chloroplast clustering, chloroplast clustering caused by the overexpression of the Nicotiana benthamiana chloroplast outer membrane protein 24 (NbOMP24) promoted the infection by PSTVd, a viroid pathogen, in N. benthamiana. Interestingly, H(2)O(2) treatment, which caused increased ROS accumulation, showed no significant effects on PSTVd infection. Moreover, NbOMP24 protein showed no direct interaction with PSTVd. We propose that perinuclear chloroplast clustering induced by NbOMP24 provides a favourable environment for PSTVd infection. These findings highlight the complexity of chloroplast clustering‐mediated plant–pathogen interactions and the need for further research to fully understand these mechanisms. John Wiley and Sons Inc. 2023-09-11 /pmc/articles/PMC10632781/ /pubmed/37695572 http://dx.doi.org/10.1111/mpp.13385 Text en © 2023 The Authors. Molecular Plant Pathology published by British Society for Plant Pathology and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Short Communication Han, Kelei Jia, Zhaoxing Zhang, Yuhong Zhou, Huijie Bu, Shan Chen, Jianping Yan, Dankan Qi, Rende Yan, Fei Wu, Jian Chloroplast clustering around the nucleus induced by OMP24 overexpression unexpectedly promoted PSTVd infection in Nicotiana benthamiana |
title | Chloroplast clustering around the nucleus induced by OMP24 overexpression unexpectedly promoted PSTVd infection in Nicotiana benthamiana
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title_full | Chloroplast clustering around the nucleus induced by OMP24 overexpression unexpectedly promoted PSTVd infection in Nicotiana benthamiana
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title_fullStr | Chloroplast clustering around the nucleus induced by OMP24 overexpression unexpectedly promoted PSTVd infection in Nicotiana benthamiana
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title_full_unstemmed | Chloroplast clustering around the nucleus induced by OMP24 overexpression unexpectedly promoted PSTVd infection in Nicotiana benthamiana
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title_short | Chloroplast clustering around the nucleus induced by OMP24 overexpression unexpectedly promoted PSTVd infection in Nicotiana benthamiana
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title_sort | chloroplast clustering around the nucleus induced by omp24 overexpression unexpectedly promoted pstvd infection in nicotiana benthamiana |
topic | Short Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10632781/ https://www.ncbi.nlm.nih.gov/pubmed/37695572 http://dx.doi.org/10.1111/mpp.13385 |
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