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A plant RNA virus inhibits NPR1 sumoylation and subverts NPR1-mediated plant immunity

NONEXPRESSER OF PATHOGENESIS-RELATED GENES 1 (NPR1) is the master regulator of salicylic acid-mediated basal and systemic acquired resistance in plants. Here, we report that NPR1 plays a pivotal role in restricting compatible infection by turnip mosaic virus, a member of the largest plant RNA virus...

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Autores principales: Liu, Jiahui, Wu, Xiaoyun, Fang, Yue, Liu, Ye, Bello, Esther Oreofe, Li, Yong, Xiong, Ruyi, Li, Yinzi, Fu, Zheng Qing, Wang, Aiming, Cheng, Xiaofei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10275998/
https://www.ncbi.nlm.nih.gov/pubmed/37328517
http://dx.doi.org/10.1038/s41467-023-39254-2
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author Liu, Jiahui
Wu, Xiaoyun
Fang, Yue
Liu, Ye
Bello, Esther Oreofe
Li, Yong
Xiong, Ruyi
Li, Yinzi
Fu, Zheng Qing
Wang, Aiming
Cheng, Xiaofei
author_facet Liu, Jiahui
Wu, Xiaoyun
Fang, Yue
Liu, Ye
Bello, Esther Oreofe
Li, Yong
Xiong, Ruyi
Li, Yinzi
Fu, Zheng Qing
Wang, Aiming
Cheng, Xiaofei
author_sort Liu, Jiahui
collection PubMed
description NONEXPRESSER OF PATHOGENESIS-RELATED GENES 1 (NPR1) is the master regulator of salicylic acid-mediated basal and systemic acquired resistance in plants. Here, we report that NPR1 plays a pivotal role in restricting compatible infection by turnip mosaic virus, a member of the largest plant RNA virus genus Potyvirus, and that such resistance is counteracted by NUCLEAR INCLUSION B (NIb), the viral RNA-dependent RNA polymerase. We demonstrate that NIb binds to the SUMO-interacting motif 3 (SIM3) of NPR1 to prevent SUMO3 interaction and sumoylation, while sumoylation of NIb by SUMO3 is not essential but can intensify the NIb–NPR1 interaction. We discover that the interaction also impedes the phosphorylation of NPR1 at Ser11/Ser15. Moreover, we show that targeting NPR1 SIM3 is a conserved ability of NIb from diverse potyviruses. These data reveal a molecular “arms race” by which potyviruses deploy NIb to suppress NPR1-mediated resistance through disrupting NPR1 sumoylation.
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spelling pubmed-102759982023-06-18 A plant RNA virus inhibits NPR1 sumoylation and subverts NPR1-mediated plant immunity Liu, Jiahui Wu, Xiaoyun Fang, Yue Liu, Ye Bello, Esther Oreofe Li, Yong Xiong, Ruyi Li, Yinzi Fu, Zheng Qing Wang, Aiming Cheng, Xiaofei Nat Commun Article NONEXPRESSER OF PATHOGENESIS-RELATED GENES 1 (NPR1) is the master regulator of salicylic acid-mediated basal and systemic acquired resistance in plants. Here, we report that NPR1 plays a pivotal role in restricting compatible infection by turnip mosaic virus, a member of the largest plant RNA virus genus Potyvirus, and that such resistance is counteracted by NUCLEAR INCLUSION B (NIb), the viral RNA-dependent RNA polymerase. We demonstrate that NIb binds to the SUMO-interacting motif 3 (SIM3) of NPR1 to prevent SUMO3 interaction and sumoylation, while sumoylation of NIb by SUMO3 is not essential but can intensify the NIb–NPR1 interaction. We discover that the interaction also impedes the phosphorylation of NPR1 at Ser11/Ser15. Moreover, we show that targeting NPR1 SIM3 is a conserved ability of NIb from diverse potyviruses. These data reveal a molecular “arms race” by which potyviruses deploy NIb to suppress NPR1-mediated resistance through disrupting NPR1 sumoylation. Nature Publishing Group UK 2023-06-16 /pmc/articles/PMC10275998/ /pubmed/37328517 http://dx.doi.org/10.1038/s41467-023-39254-2 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Liu, Jiahui
Wu, Xiaoyun
Fang, Yue
Liu, Ye
Bello, Esther Oreofe
Li, Yong
Xiong, Ruyi
Li, Yinzi
Fu, Zheng Qing
Wang, Aiming
Cheng, Xiaofei
A plant RNA virus inhibits NPR1 sumoylation and subverts NPR1-mediated plant immunity
title A plant RNA virus inhibits NPR1 sumoylation and subverts NPR1-mediated plant immunity
title_full A plant RNA virus inhibits NPR1 sumoylation and subverts NPR1-mediated plant immunity
title_fullStr A plant RNA virus inhibits NPR1 sumoylation and subverts NPR1-mediated plant immunity
title_full_unstemmed A plant RNA virus inhibits NPR1 sumoylation and subverts NPR1-mediated plant immunity
title_short A plant RNA virus inhibits NPR1 sumoylation and subverts NPR1-mediated plant immunity
title_sort plant rna virus inhibits npr1 sumoylation and subverts npr1-mediated plant immunity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10275998/
https://www.ncbi.nlm.nih.gov/pubmed/37328517
http://dx.doi.org/10.1038/s41467-023-39254-2
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