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RNAi‐mediated stable silencing of TaCSN5 confers broad‐spectrum resistance to Puccinia striiformis f. sp. tritici
The constitutive photomorphogenesis 9 (COP9) signalosome (CSN) is a versatile regulator of plant growth, development, and response to diverse pathogens. However, little research has been done to understand the function of those CSN genes in broad‐spectrum resistance to pathogens. In this study, we f...
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/PMC7938628/ https://www.ncbi.nlm.nih.gov/pubmed/33486803 http://dx.doi.org/10.1111/mpp.13034 |
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author | Bai, Xingxuan Huang, Xueling Tian, Shuxin Peng, Huan Zhan, Gangming Goher, Farhan Guo, Jia Kang, Zhensheng Guo, Jun |
author_facet | Bai, Xingxuan Huang, Xueling Tian, Shuxin Peng, Huan Zhan, Gangming Goher, Farhan Guo, Jia Kang, Zhensheng Guo, Jun |
author_sort | Bai, Xingxuan |
collection | PubMed |
description | The constitutive photomorphogenesis 9 (COP9) signalosome (CSN) is a versatile regulator of plant growth, development, and response to diverse pathogens. However, little research has been done to understand the function of those CSN genes in broad‐spectrum resistance to pathogens. In this study, we found that the transcript levels of wheat TaCSN5 were induced in response to inoculation with Puccinia striiformis f. sp. tritici (Pst) and treatment with salicylic acid (SA). Overexpression of TaCSN5 in Arabidopsis resulted in increased susceptibility to Pseudomonas syringae pv. tomato DC3000 infection accompanied by down‐regulation of AtPR1 expression. Overexpression of TaCSN5 in wheat lines significantly increased susceptibility to Pst accompanied by decreased SA accumulation, whereas TaCSN5‐RNAi wheat lines exhibited opposite trends. Moreover, we found that TaCSN5 negatively regulated TaG3NPR1 genes involved in the SA signalling pathway. In addition, TaCSN5‐RNAi lines showed increased resistance to multiple races of Pst. Taken together, we demonstrate that TaCSN5 contributes to negative regulation of wheat resistance to Pst in an SA‐dependent manner. |
format | Online Article Text |
id | pubmed-7938628 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-79386282021-03-16 RNAi‐mediated stable silencing of TaCSN5 confers broad‐spectrum resistance to Puccinia striiformis f. sp. tritici Bai, Xingxuan Huang, Xueling Tian, Shuxin Peng, Huan Zhan, Gangming Goher, Farhan Guo, Jia Kang, Zhensheng Guo, Jun Mol Plant Pathol Original Articles The constitutive photomorphogenesis 9 (COP9) signalosome (CSN) is a versatile regulator of plant growth, development, and response to diverse pathogens. However, little research has been done to understand the function of those CSN genes in broad‐spectrum resistance to pathogens. In this study, we found that the transcript levels of wheat TaCSN5 were induced in response to inoculation with Puccinia striiformis f. sp. tritici (Pst) and treatment with salicylic acid (SA). Overexpression of TaCSN5 in Arabidopsis resulted in increased susceptibility to Pseudomonas syringae pv. tomato DC3000 infection accompanied by down‐regulation of AtPR1 expression. Overexpression of TaCSN5 in wheat lines significantly increased susceptibility to Pst accompanied by decreased SA accumulation, whereas TaCSN5‐RNAi wheat lines exhibited opposite trends. Moreover, we found that TaCSN5 negatively regulated TaG3NPR1 genes involved in the SA signalling pathway. In addition, TaCSN5‐RNAi lines showed increased resistance to multiple races of Pst. Taken together, we demonstrate that TaCSN5 contributes to negative regulation of wheat resistance to Pst in an SA‐dependent manner. John Wiley and Sons Inc. 2021-01-24 /pmc/articles/PMC7938628/ /pubmed/33486803 http://dx.doi.org/10.1111/mpp.13034 Text en © 2021 The Authors. Molecular Plant Pathology published by British Society for Plant Pathology and John Wiley & Sons Ltd 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 | Original Articles Bai, Xingxuan Huang, Xueling Tian, Shuxin Peng, Huan Zhan, Gangming Goher, Farhan Guo, Jia Kang, Zhensheng Guo, Jun RNAi‐mediated stable silencing of TaCSN5 confers broad‐spectrum resistance to Puccinia striiformis f. sp. tritici |
title | RNAi‐mediated stable silencing of TaCSN5 confers broad‐spectrum resistance to Puccinia striiformis f. sp. tritici
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title_full | RNAi‐mediated stable silencing of TaCSN5 confers broad‐spectrum resistance to Puccinia striiformis f. sp. tritici
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title_fullStr | RNAi‐mediated stable silencing of TaCSN5 confers broad‐spectrum resistance to Puccinia striiformis f. sp. tritici
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title_full_unstemmed | RNAi‐mediated stable silencing of TaCSN5 confers broad‐spectrum resistance to Puccinia striiformis f. sp. tritici
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title_short | RNAi‐mediated stable silencing of TaCSN5 confers broad‐spectrum resistance to Puccinia striiformis f. sp. tritici
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title_sort | rnai‐mediated stable silencing of tacsn5 confers broad‐spectrum resistance to puccinia striiformis f. sp. tritici |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7938628/ https://www.ncbi.nlm.nih.gov/pubmed/33486803 http://dx.doi.org/10.1111/mpp.13034 |
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