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A fungal effector targets a heat shock–dynamin protein complex to modulate mitochondrial dynamics and reduce plant immunity

Mitochondria are essential for animal and plant immunity. Here, we report that the effector MoCDIP4 of the fungal pathogen Magnaporthe oryzae targets the mitochondria-associated OsDjA9-OsDRP1E protein complex to reduce rice immunity. The DnaJ protein OsDjA9 interacts with the dynamin-related protein...

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Autores principales: Xu, Guojuan, Zhong, Xionghui, Shi, Yanlong, Liu, Zhuo, Jiang, Nan, Liu, Jing, Ding, Bo, Li, Zhiqiang, Kang, Houxiang, Ning, Yuese, Liu, Wende, Guo, Zejian, Wang, Guo-Liang, Wang, Xuli
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7688324/
https://www.ncbi.nlm.nih.gov/pubmed/33239288
http://dx.doi.org/10.1126/sciadv.abb7719
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author Xu, Guojuan
Zhong, Xionghui
Shi, Yanlong
Liu, Zhuo
Jiang, Nan
Liu, Jing
Ding, Bo
Li, Zhiqiang
Kang, Houxiang
Ning, Yuese
Liu, Wende
Guo, Zejian
Wang, Guo-Liang
Wang, Xuli
author_facet Xu, Guojuan
Zhong, Xionghui
Shi, Yanlong
Liu, Zhuo
Jiang, Nan
Liu, Jing
Ding, Bo
Li, Zhiqiang
Kang, Houxiang
Ning, Yuese
Liu, Wende
Guo, Zejian
Wang, Guo-Liang
Wang, Xuli
author_sort Xu, Guojuan
collection PubMed
description Mitochondria are essential for animal and plant immunity. Here, we report that the effector MoCDIP4 of the fungal pathogen Magnaporthe oryzae targets the mitochondria-associated OsDjA9-OsDRP1E protein complex to reduce rice immunity. The DnaJ protein OsDjA9 interacts with the dynamin-related protein OsDRP1E and promotes the degradation of OsDRP1E, which functions in mitochondrial fission. By contrast, MoCDIP4 binds OsDjA9 to compete with OsDRP1E, resulting in OsDRP1E accumulation. Knockout of OsDjA9 or overexpression of OsDRP1E or MoCDIP4 in transgenic rice results in shortened mitochondria and enhanced susceptibility to M. oryzae. Overexpression of OsDjA9 or knockout of OsDRP1E in transgenic rice, in contrast, leads to elongated mitochondria and enhanced resistance to M. oryzae. Our study therefore reveals a previously unidentified pathogen-infection strategy in which the pathogen delivers an effector into plant cells to target an HSP40-DRP complex; the targeting leads to the perturbation of mitochondrial dynamics, thereby inhibiting mitochondria-mediated plant immunity.
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spelling pubmed-76883242020-12-03 A fungal effector targets a heat shock–dynamin protein complex to modulate mitochondrial dynamics and reduce plant immunity Xu, Guojuan Zhong, Xionghui Shi, Yanlong Liu, Zhuo Jiang, Nan Liu, Jing Ding, Bo Li, Zhiqiang Kang, Houxiang Ning, Yuese Liu, Wende Guo, Zejian Wang, Guo-Liang Wang, Xuli Sci Adv Research Articles Mitochondria are essential for animal and plant immunity. Here, we report that the effector MoCDIP4 of the fungal pathogen Magnaporthe oryzae targets the mitochondria-associated OsDjA9-OsDRP1E protein complex to reduce rice immunity. The DnaJ protein OsDjA9 interacts with the dynamin-related protein OsDRP1E and promotes the degradation of OsDRP1E, which functions in mitochondrial fission. By contrast, MoCDIP4 binds OsDjA9 to compete with OsDRP1E, resulting in OsDRP1E accumulation. Knockout of OsDjA9 or overexpression of OsDRP1E or MoCDIP4 in transgenic rice results in shortened mitochondria and enhanced susceptibility to M. oryzae. Overexpression of OsDjA9 or knockout of OsDRP1E in transgenic rice, in contrast, leads to elongated mitochondria and enhanced resistance to M. oryzae. Our study therefore reveals a previously unidentified pathogen-infection strategy in which the pathogen delivers an effector into plant cells to target an HSP40-DRP complex; the targeting leads to the perturbation of mitochondrial dynamics, thereby inhibiting mitochondria-mediated plant immunity. American Association for the Advancement of Science 2020-11-25 /pmc/articles/PMC7688324/ /pubmed/33239288 http://dx.doi.org/10.1126/sciadv.abb7719 Text en Copyright © 2020 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/ https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited.
spellingShingle Research Articles
Xu, Guojuan
Zhong, Xionghui
Shi, Yanlong
Liu, Zhuo
Jiang, Nan
Liu, Jing
Ding, Bo
Li, Zhiqiang
Kang, Houxiang
Ning, Yuese
Liu, Wende
Guo, Zejian
Wang, Guo-Liang
Wang, Xuli
A fungal effector targets a heat shock–dynamin protein complex to modulate mitochondrial dynamics and reduce plant immunity
title A fungal effector targets a heat shock–dynamin protein complex to modulate mitochondrial dynamics and reduce plant immunity
title_full A fungal effector targets a heat shock–dynamin protein complex to modulate mitochondrial dynamics and reduce plant immunity
title_fullStr A fungal effector targets a heat shock–dynamin protein complex to modulate mitochondrial dynamics and reduce plant immunity
title_full_unstemmed A fungal effector targets a heat shock–dynamin protein complex to modulate mitochondrial dynamics and reduce plant immunity
title_short A fungal effector targets a heat shock–dynamin protein complex to modulate mitochondrial dynamics and reduce plant immunity
title_sort fungal effector targets a heat shock–dynamin protein complex to modulate mitochondrial dynamics and reduce plant immunity
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7688324/
https://www.ncbi.nlm.nih.gov/pubmed/33239288
http://dx.doi.org/10.1126/sciadv.abb7719
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