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Silencing of the calcium-dependent protein kinase TaCDPK27 improves wheat resistance to powdery mildew

BACKGROUND: Calcium ions (Ca(2+)), secondary messengers, are crucial for the signal transduction process of the interaction between plants and pathogens. Ca(2+) signaling also regulates autophagy. As plant calcium signal-decoding proteins, calcium-dependent protein kinases (CDPKs) have been found to...

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Autores principales: Yue, Jie-yu, Jiao, Jin-lan, Wang, Wen-wen, Jie, Xin-rui, Wang, Hua-zhong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9993671/
https://www.ncbi.nlm.nih.gov/pubmed/36882703
http://dx.doi.org/10.1186/s12870-023-04140-y
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author Yue, Jie-yu
Jiao, Jin-lan
Wang, Wen-wen
Jie, Xin-rui
Wang, Hua-zhong
author_facet Yue, Jie-yu
Jiao, Jin-lan
Wang, Wen-wen
Jie, Xin-rui
Wang, Hua-zhong
author_sort Yue, Jie-yu
collection PubMed
description BACKGROUND: Calcium ions (Ca(2+)), secondary messengers, are crucial for the signal transduction process of the interaction between plants and pathogens. Ca(2+) signaling also regulates autophagy. As plant calcium signal-decoding proteins, calcium-dependent protein kinases (CDPKs) have been found to be involved in biotic and abiotic stress responses. However, information on their functions in response to powdery mildew attack in wheat crops is limited. RESULT: In the present study, the expression levels of TaCDPK27, four essential autophagy-related genes (ATGs) (TaATG5, TaATG7, TaATG8, and TaATG10), and two major metacaspase genes, namely, TaMCA1 and TaMCA9, were increased by powdery mildew (Blumeria graminis f. sp. tritici, Bgt) infection in wheat seedling leaves. Silencing TaCDPK27 improves wheat seedling resistance to powdery mildew, with fewer Bgt hyphae occurring on TaCDPK27-silenced wheat seedling leaves than on normal seedlings. In wheat seedling leaves under powdery mildew infection, silencing TaCDPK27 induced excess contents of reactive oxygen species (ROS); decreased the activities of superoxide dismutase (SOD), peroxidase (POD) and catalase (CAT); and led to an increase in programmed cell death (PCD). Silencing TaCDPK27 also inhibited autophagy in wheat seedling leaves, and silencing TaATG7 also enhanced wheat seedling resistance to powdery mildew infection. TaCDPK27-mCherry and GFP-TaATG8h colocalized in wheat protoplasts. Overexpressed TaCDPK27-mCherry fusions required enhanced autophagy activity in wheat protoplast under carbon starvation. CONCLUSION: These results suggested that TaCDPK27 negatively regulates wheat resistance to PW infection, and functionally links with autophagy in wheat.
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spelling pubmed-99936712023-03-09 Silencing of the calcium-dependent protein kinase TaCDPK27 improves wheat resistance to powdery mildew Yue, Jie-yu Jiao, Jin-lan Wang, Wen-wen Jie, Xin-rui Wang, Hua-zhong BMC Plant Biol Research BACKGROUND: Calcium ions (Ca(2+)), secondary messengers, are crucial for the signal transduction process of the interaction between plants and pathogens. Ca(2+) signaling also regulates autophagy. As plant calcium signal-decoding proteins, calcium-dependent protein kinases (CDPKs) have been found to be involved in biotic and abiotic stress responses. However, information on their functions in response to powdery mildew attack in wheat crops is limited. RESULT: In the present study, the expression levels of TaCDPK27, four essential autophagy-related genes (ATGs) (TaATG5, TaATG7, TaATG8, and TaATG10), and two major metacaspase genes, namely, TaMCA1 and TaMCA9, were increased by powdery mildew (Blumeria graminis f. sp. tritici, Bgt) infection in wheat seedling leaves. Silencing TaCDPK27 improves wheat seedling resistance to powdery mildew, with fewer Bgt hyphae occurring on TaCDPK27-silenced wheat seedling leaves than on normal seedlings. In wheat seedling leaves under powdery mildew infection, silencing TaCDPK27 induced excess contents of reactive oxygen species (ROS); decreased the activities of superoxide dismutase (SOD), peroxidase (POD) and catalase (CAT); and led to an increase in programmed cell death (PCD). Silencing TaCDPK27 also inhibited autophagy in wheat seedling leaves, and silencing TaATG7 also enhanced wheat seedling resistance to powdery mildew infection. TaCDPK27-mCherry and GFP-TaATG8h colocalized in wheat protoplasts. Overexpressed TaCDPK27-mCherry fusions required enhanced autophagy activity in wheat protoplast under carbon starvation. CONCLUSION: These results suggested that TaCDPK27 negatively regulates wheat resistance to PW infection, and functionally links with autophagy in wheat. BioMed Central 2023-03-08 /pmc/articles/PMC9993671/ /pubmed/36882703 http://dx.doi.org/10.1186/s12870-023-04140-y Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Yue, Jie-yu
Jiao, Jin-lan
Wang, Wen-wen
Jie, Xin-rui
Wang, Hua-zhong
Silencing of the calcium-dependent protein kinase TaCDPK27 improves wheat resistance to powdery mildew
title Silencing of the calcium-dependent protein kinase TaCDPK27 improves wheat resistance to powdery mildew
title_full Silencing of the calcium-dependent protein kinase TaCDPK27 improves wheat resistance to powdery mildew
title_fullStr Silencing of the calcium-dependent protein kinase TaCDPK27 improves wheat resistance to powdery mildew
title_full_unstemmed Silencing of the calcium-dependent protein kinase TaCDPK27 improves wheat resistance to powdery mildew
title_short Silencing of the calcium-dependent protein kinase TaCDPK27 improves wheat resistance to powdery mildew
title_sort silencing of the calcium-dependent protein kinase tacdpk27 improves wheat resistance to powdery mildew
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9993671/
https://www.ncbi.nlm.nih.gov/pubmed/36882703
http://dx.doi.org/10.1186/s12870-023-04140-y
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