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Two interacting transcriptional coactivators cooperatively control plant immune responses

The phytohormone salicylic acid (SA) plays a pivotal role in plant defense against biotrophic and hemibiotrophic pathogens. NPR1 and EDS1 function as two central hubs in plant local and systemic immunity. However, it is unclear how NPR1 orchestrates gene regulation and whether EDS1 directly particip...

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Autores principales: Chen, Huan, Li, Min, Qi, Guang, Zhao, Ming, Liu, Longyu, Zhang, Jingyi, Chen, Gongyou, Wang, Daowen, Liu, Fengquan, Fu, Zheng Qing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8570602/
https://www.ncbi.nlm.nih.gov/pubmed/34739308
http://dx.doi.org/10.1126/sciadv.abl7173
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author Chen, Huan
Li, Min
Qi, Guang
Zhao, Ming
Liu, Longyu
Zhang, Jingyi
Chen, Gongyou
Wang, Daowen
Liu, Fengquan
Fu, Zheng Qing
author_facet Chen, Huan
Li, Min
Qi, Guang
Zhao, Ming
Liu, Longyu
Zhang, Jingyi
Chen, Gongyou
Wang, Daowen
Liu, Fengquan
Fu, Zheng Qing
author_sort Chen, Huan
collection PubMed
description The phytohormone salicylic acid (SA) plays a pivotal role in plant defense against biotrophic and hemibiotrophic pathogens. NPR1 and EDS1 function as two central hubs in plant local and systemic immunity. However, it is unclear how NPR1 orchestrates gene regulation and whether EDS1 directly participates in transcriptional reprogramming. Here, we show that NPR1 and EDS1 synergistically activate pathogenesis-related (PR) genes and plant defenses by forming a protein complex and recruiting Mediator. We discover that EDS1 functions as an autonomous transcriptional coactivator with intrinsic transactivation domains and physically interacts with the CDK8 subunit of Mediator. Upon SA induction, EDS1 is directly recruited by NPR1 onto the PR1 promoter via physical NPR1-EDS1 interactions, thereby potentiating PR1 activation. We further demonstrate that EDS1 stabilizes NPR1 protein and NPR1 transcriptionally up-regulates EDS1. Our results reveal an elegant interplay of key coactivators with Mediator and elucidate important molecular mechanisms for activating transcription during immune responses.
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spelling pubmed-85706022021-11-17 Two interacting transcriptional coactivators cooperatively control plant immune responses Chen, Huan Li, Min Qi, Guang Zhao, Ming Liu, Longyu Zhang, Jingyi Chen, Gongyou Wang, Daowen Liu, Fengquan Fu, Zheng Qing Sci Adv Biomedicine and Life Sciences The phytohormone salicylic acid (SA) plays a pivotal role in plant defense against biotrophic and hemibiotrophic pathogens. NPR1 and EDS1 function as two central hubs in plant local and systemic immunity. However, it is unclear how NPR1 orchestrates gene regulation and whether EDS1 directly participates in transcriptional reprogramming. Here, we show that NPR1 and EDS1 synergistically activate pathogenesis-related (PR) genes and plant defenses by forming a protein complex and recruiting Mediator. We discover that EDS1 functions as an autonomous transcriptional coactivator with intrinsic transactivation domains and physically interacts with the CDK8 subunit of Mediator. Upon SA induction, EDS1 is directly recruited by NPR1 onto the PR1 promoter via physical NPR1-EDS1 interactions, thereby potentiating PR1 activation. We further demonstrate that EDS1 stabilizes NPR1 protein and NPR1 transcriptionally up-regulates EDS1. Our results reveal an elegant interplay of key coactivators with Mediator and elucidate important molecular mechanisms for activating transcription during immune responses. American Association for the Advancement of Science 2021-11-05 /pmc/articles/PMC8570602/ /pubmed/34739308 http://dx.doi.org/10.1126/sciadv.abl7173 Text en Copyright © 2021 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/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 Biomedicine and Life Sciences
Chen, Huan
Li, Min
Qi, Guang
Zhao, Ming
Liu, Longyu
Zhang, Jingyi
Chen, Gongyou
Wang, Daowen
Liu, Fengquan
Fu, Zheng Qing
Two interacting transcriptional coactivators cooperatively control plant immune responses
title Two interacting transcriptional coactivators cooperatively control plant immune responses
title_full Two interacting transcriptional coactivators cooperatively control plant immune responses
title_fullStr Two interacting transcriptional coactivators cooperatively control plant immune responses
title_full_unstemmed Two interacting transcriptional coactivators cooperatively control plant immune responses
title_short Two interacting transcriptional coactivators cooperatively control plant immune responses
title_sort two interacting transcriptional coactivators cooperatively control plant immune responses
topic Biomedicine and Life Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8570602/
https://www.ncbi.nlm.nih.gov/pubmed/34739308
http://dx.doi.org/10.1126/sciadv.abl7173
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