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A new mode of NPR1 action via an NB‐ARC–NPR1 fusion protein negatively regulates the defence response in wheat to stem rust pathogen

NPR1 has been found to be a key transcriptional regulator in some plant defence responses. There are nine NPR1 homologues (TaNPR1) in wheat, but little research has been done to understand the function of those NPR1‐like genes in the wheat defence response against stem rust (Puccinia graminis f. sp....

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Autores principales: Wang, Xiaojing, Zhang, Hongtao, Nyamesorto, Bernard, Luo, Yi, Mu, Xiaoqian, Wang, Fangyan, Kang, Zhensheng, Lagudah, Evans, Huang, Li
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7589253/
https://www.ncbi.nlm.nih.gov/pubmed/32544264
http://dx.doi.org/10.1111/nph.16748
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author Wang, Xiaojing
Zhang, Hongtao
Nyamesorto, Bernard
Luo, Yi
Mu, Xiaoqian
Wang, Fangyan
Kang, Zhensheng
Lagudah, Evans
Huang, Li
author_facet Wang, Xiaojing
Zhang, Hongtao
Nyamesorto, Bernard
Luo, Yi
Mu, Xiaoqian
Wang, Fangyan
Kang, Zhensheng
Lagudah, Evans
Huang, Li
author_sort Wang, Xiaojing
collection PubMed
description NPR1 has been found to be a key transcriptional regulator in some plant defence responses. There are nine NPR1 homologues (TaNPR1) in wheat, but little research has been done to understand the function of those NPR1‐like genes in the wheat defence response against stem rust (Puccinia graminis f. sp. tritici) pathogens. We used bioinformatics and reverse genetics approaches to study the expression and function of each TaNPR1. We found six members of TaNPR1 located on homoeologous group 3 chromosomes (designated as TaG3NPR1) and three on homoeologous group 7 chromosomes (designated as TaG7NPR1). The group 3 NPR1 proteins regulate transcription of SA‐responsive PR genes. Downregulation of all the TaNPR1 homologues via virus‐induced gene co‐silencing resulted in enhanced resistance to stem rust. More specifically downregulating TaG7NPR1 homeologues or Ta7ANPR1 expression resulted in stem rust resistance phenotype. By contrast, knocking down TaG3NPR1 alone did not show visible phenotypic changes in response to the rust pathogen. Knocking out Ta7ANPR1 enhanced resistance to stem rust. The Ta7ANPR1 locus is alternatively spliced under pathogen inoculated conditions. We discovered a new mode of NPR1 action in wheat at the Ta7ANPR1 locus through an NB‐ARC–NPR1 fusion protein negatively regulating the defence to stem rust infection.
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spelling pubmed-75892532020-10-30 A new mode of NPR1 action via an NB‐ARC–NPR1 fusion protein negatively regulates the defence response in wheat to stem rust pathogen Wang, Xiaojing Zhang, Hongtao Nyamesorto, Bernard Luo, Yi Mu, Xiaoqian Wang, Fangyan Kang, Zhensheng Lagudah, Evans Huang, Li New Phytol Research NPR1 has been found to be a key transcriptional regulator in some plant defence responses. There are nine NPR1 homologues (TaNPR1) in wheat, but little research has been done to understand the function of those NPR1‐like genes in the wheat defence response against stem rust (Puccinia graminis f. sp. tritici) pathogens. We used bioinformatics and reverse genetics approaches to study the expression and function of each TaNPR1. We found six members of TaNPR1 located on homoeologous group 3 chromosomes (designated as TaG3NPR1) and three on homoeologous group 7 chromosomes (designated as TaG7NPR1). The group 3 NPR1 proteins regulate transcription of SA‐responsive PR genes. Downregulation of all the TaNPR1 homologues via virus‐induced gene co‐silencing resulted in enhanced resistance to stem rust. More specifically downregulating TaG7NPR1 homeologues or Ta7ANPR1 expression resulted in stem rust resistance phenotype. By contrast, knocking down TaG3NPR1 alone did not show visible phenotypic changes in response to the rust pathogen. Knocking out Ta7ANPR1 enhanced resistance to stem rust. The Ta7ANPR1 locus is alternatively spliced under pathogen inoculated conditions. We discovered a new mode of NPR1 action in wheat at the Ta7ANPR1 locus through an NB‐ARC–NPR1 fusion protein negatively regulating the defence to stem rust infection. John Wiley and Sons Inc. 2020-08-26 2020-11 /pmc/articles/PMC7589253/ /pubmed/32544264 http://dx.doi.org/10.1111/nph.16748 Text en ©2020 The Authors. New Phytologist ©2020 New Phytologist Trust This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Research
Wang, Xiaojing
Zhang, Hongtao
Nyamesorto, Bernard
Luo, Yi
Mu, Xiaoqian
Wang, Fangyan
Kang, Zhensheng
Lagudah, Evans
Huang, Li
A new mode of NPR1 action via an NB‐ARC–NPR1 fusion protein negatively regulates the defence response in wheat to stem rust pathogen
title A new mode of NPR1 action via an NB‐ARC–NPR1 fusion protein negatively regulates the defence response in wheat to stem rust pathogen
title_full A new mode of NPR1 action via an NB‐ARC–NPR1 fusion protein negatively regulates the defence response in wheat to stem rust pathogen
title_fullStr A new mode of NPR1 action via an NB‐ARC–NPR1 fusion protein negatively regulates the defence response in wheat to stem rust pathogen
title_full_unstemmed A new mode of NPR1 action via an NB‐ARC–NPR1 fusion protein negatively regulates the defence response in wheat to stem rust pathogen
title_short A new mode of NPR1 action via an NB‐ARC–NPR1 fusion protein negatively regulates the defence response in wheat to stem rust pathogen
title_sort new mode of npr1 action via an nb‐arc–npr1 fusion protein negatively regulates the defence response in wheat to stem rust pathogen
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7589253/
https://www.ncbi.nlm.nih.gov/pubmed/32544264
http://dx.doi.org/10.1111/nph.16748
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