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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...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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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. |
format | Online Article Text |
id | pubmed-8131040 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
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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