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The CC‐NB‐LRR OsRLR1 mediates rice disease resistance through interaction with OsWRKY19

Nucleotide‐binding site–leucine‐rich repeat (NB‐LRR) resistance proteins are critical for plant resistance to pathogens; however, their mechanism of activation and signal transduction is still not well understood. We identified a mutation in an as yet uncharacterized rice coiled‐coil (CC)‐NB‐LRR, Or...

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Autores principales: Du, Dan, Zhang, Changwei, Xing, Yadi, Lu, Xin, Cai, Linjun, Yun, Han, Zhang, Qiuli, Zhang, Yingying, Chen, Xinlong, Liu, Mingming, Sang, Xianchun, Ling, Yinghua, Yang, Zhenglin, Li, Yunfeng, Lefebvre, Benoit, He, Guanghua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8131040/
https://www.ncbi.nlm.nih.gov/pubmed/33368943
http://dx.doi.org/10.1111/pbi.13530
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author Du, Dan
Zhang, Changwei
Xing, Yadi
Lu, Xin
Cai, Linjun
Yun, Han
Zhang, Qiuli
Zhang, Yingying
Chen, Xinlong
Liu, Mingming
Sang, Xianchun
Ling, Yinghua
Yang, Zhenglin
Li, Yunfeng
Lefebvre, Benoit
He, Guanghua
author_facet Du, Dan
Zhang, Changwei
Xing, Yadi
Lu, Xin
Cai, Linjun
Yun, Han
Zhang, Qiuli
Zhang, Yingying
Chen, Xinlong
Liu, Mingming
Sang, Xianchun
Ling, Yinghua
Yang, Zhenglin
Li, Yunfeng
Lefebvre, Benoit
He, Guanghua
author_sort Du, Dan
collection PubMed
description Nucleotide‐binding site–leucine‐rich repeat (NB‐LRR) resistance proteins are critical for plant resistance to pathogens; however, their mechanism of activation and signal transduction is still not well understood. We identified a mutation in an as yet uncharacterized rice coiled‐coil (CC)‐NB‐LRR, Oryza sativa RPM1‐like resistance gene 1 (OsRLR1), which leads to hypersensitive response (HR)‐like lesions on the leaf blade and broad‐range resistance to the fungal pathogen Pyricularia oryzae (syn. Magnaporthe oryzae) and the bacterial pathogen Xanthomonas oryzae pv. oryzae, together with strong growth reduction. Consistently, OsRLR1‐overexpression lines showed enhanced resistance to both pathogens. Moreover, we found that OsRLR1 mediates the defence response through direct interaction in the nucleus with the transcription factor OsWRKY19. Down‐regulation of OsWRKY19 in the rlr1 mutant compromised the HR‐like phenotype and resistance response, and largely restored plant growth. OsWRKY19 binds to the promoter of OsPR10 to activate the defence response. Taken together, our data highlight the role of a new residue involved in the NB‐LRR activation mechanism, allowing identification of a new NB‐LRR downstream signalling pathway.
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spelling pubmed-81310402021-05-21 The CC‐NB‐LRR OsRLR1 mediates rice disease resistance through interaction with OsWRKY19 Du, Dan Zhang, Changwei Xing, Yadi Lu, Xin Cai, Linjun Yun, Han Zhang, Qiuli Zhang, Yingying Chen, Xinlong Liu, Mingming Sang, Xianchun Ling, Yinghua Yang, Zhenglin Li, Yunfeng Lefebvre, Benoit He, Guanghua Plant Biotechnol J Research Articles Nucleotide‐binding site–leucine‐rich repeat (NB‐LRR) resistance proteins are critical for plant resistance to pathogens; however, their mechanism of activation and signal transduction is still not well understood. We identified a mutation in an as yet uncharacterized rice coiled‐coil (CC)‐NB‐LRR, Oryza sativa RPM1‐like resistance gene 1 (OsRLR1), which leads to hypersensitive response (HR)‐like lesions on the leaf blade and broad‐range resistance to the fungal pathogen Pyricularia oryzae (syn. Magnaporthe oryzae) and the bacterial pathogen Xanthomonas oryzae pv. oryzae, together with strong growth reduction. Consistently, OsRLR1‐overexpression lines showed enhanced resistance to both pathogens. Moreover, we found that OsRLR1 mediates the defence response through direct interaction in the nucleus with the transcription factor OsWRKY19. Down‐regulation of OsWRKY19 in the rlr1 mutant compromised the HR‐like phenotype and resistance response, and largely restored plant growth. OsWRKY19 binds to the promoter of OsPR10 to activate the defence response. Taken together, our data highlight the role of a new residue involved in the NB‐LRR activation mechanism, allowing identification of a new NB‐LRR downstream signalling pathway. John Wiley and Sons Inc. 2021-01-17 2021-05 /pmc/articles/PMC8131040/ /pubmed/33368943 http://dx.doi.org/10.1111/pbi.13530 Text en © 2020 The Authors. Plant Biotechnology Journal published by Society for Experimental Biology and The Association of Applied Biologists and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Research Articles
Du, Dan
Zhang, Changwei
Xing, Yadi
Lu, Xin
Cai, Linjun
Yun, Han
Zhang, Qiuli
Zhang, Yingying
Chen, Xinlong
Liu, Mingming
Sang, Xianchun
Ling, Yinghua
Yang, Zhenglin
Li, Yunfeng
Lefebvre, Benoit
He, Guanghua
The CC‐NB‐LRR OsRLR1 mediates rice disease resistance through interaction with OsWRKY19
title The CC‐NB‐LRR OsRLR1 mediates rice disease resistance through interaction with OsWRKY19
title_full The CC‐NB‐LRR OsRLR1 mediates rice disease resistance through interaction with OsWRKY19
title_fullStr The CC‐NB‐LRR OsRLR1 mediates rice disease resistance through interaction with OsWRKY19
title_full_unstemmed The CC‐NB‐LRR OsRLR1 mediates rice disease resistance through interaction with OsWRKY19
title_short The CC‐NB‐LRR OsRLR1 mediates rice disease resistance through interaction with OsWRKY19
title_sort cc‐nb‐lrr osrlr1 mediates rice disease resistance through interaction with oswrky19
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8131040/
https://www.ncbi.nlm.nih.gov/pubmed/33368943
http://dx.doi.org/10.1111/pbi.13530
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