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Potato calcineurin B-like protein CBL4, interacting with calcineurin B-like protein-interacting protein kinase CIPK2, positively regulates plant resistance to stem canker caused by Rhizoctonia solani

INTRODUCTION: Calcium sensor calcineurin B-like proteins (CBLs) and their interacting partners, CBL-interacting protein kinases (CIPKs), have emerged as a complex network in response to abiotic and biotic stress perception. However, little is known about how CBL-CIPK complexes function in potatoes....

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Autores principales: Yang, Shuai, Li, Jie, Lu, Jie, Wang, Ling, Min, Fanxiang, Guo, Mei, Wei, Qi, Wang, Wenzhong, Dong, Xuezhi, Mao, Yanzhi, Hu, Linshuang, Wang, Xiaodan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9845770/
https://www.ncbi.nlm.nih.gov/pubmed/36687567
http://dx.doi.org/10.3389/fmicb.2022.1032900
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author Yang, Shuai
Li, Jie
Lu, Jie
Wang, Ling
Min, Fanxiang
Guo, Mei
Wei, Qi
Wang, Wenzhong
Dong, Xuezhi
Mao, Yanzhi
Hu, Linshuang
Wang, Xiaodan
author_facet Yang, Shuai
Li, Jie
Lu, Jie
Wang, Ling
Min, Fanxiang
Guo, Mei
Wei, Qi
Wang, Wenzhong
Dong, Xuezhi
Mao, Yanzhi
Hu, Linshuang
Wang, Xiaodan
author_sort Yang, Shuai
collection PubMed
description INTRODUCTION: Calcium sensor calcineurin B-like proteins (CBLs) and their interacting partners, CBL-interacting protein kinases (CIPKs), have emerged as a complex network in response to abiotic and biotic stress perception. However, little is known about how CBL-CIPK complexes function in potatoes. METHODS: In this study, we identified the components of one potato signaling complex, StCBL4–StCIPK2, and characterized its function in defense against Rhizoctonia solani causing stem canker in potato. RESULTS: Expressions of both StCBL4 and StCIPK2 from potato were coordinately induced upon R. solani infection and following exposure to the defense genes. Furthermore, transient overexpression of StCBL4 and StCIPK2 individually and synergistically increased the tolerance of potato plants to R. solani in Nicotiana benthamiana. Additionally, the transgenic potato has also been shown to enhance resistance significantly. In contrast, susceptibility to R. solani was exhibited in N. benthamiana following virus-induced gene silencing of NbCBL and NbCIPK2. Evidence revealed that StCBL4 could interact in yeast and in planta with StCIPK2. StCBL4 and StCIPK2 transcription was induced upon R. solani infection and this expression in response to the pathogen was enhanced in StCBL4- and StCIPK2-transgenic potato. Moreover, accumulated expression of pathogenesis-related (PR) genes and reactive oxygen species (ROS) was significantly upregulated and enhanced in both StCBL4- and StCIPK2- transgenic potato. DISCUSSION: Accordingly, StCBL4 and StCIPK2 were involved in regulating the immune response to defend the potato plant against R. solani. Together, our data demonstrate that StCBL4 functions in concert with StCIPK2, as positive regulators of immunity, contributing to combating stem canker disease in potato.
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spelling pubmed-98457702023-01-19 Potato calcineurin B-like protein CBL4, interacting with calcineurin B-like protein-interacting protein kinase CIPK2, positively regulates plant resistance to stem canker caused by Rhizoctonia solani Yang, Shuai Li, Jie Lu, Jie Wang, Ling Min, Fanxiang Guo, Mei Wei, Qi Wang, Wenzhong Dong, Xuezhi Mao, Yanzhi Hu, Linshuang Wang, Xiaodan Front Microbiol Microbiology INTRODUCTION: Calcium sensor calcineurin B-like proteins (CBLs) and their interacting partners, CBL-interacting protein kinases (CIPKs), have emerged as a complex network in response to abiotic and biotic stress perception. However, little is known about how CBL-CIPK complexes function in potatoes. METHODS: In this study, we identified the components of one potato signaling complex, StCBL4–StCIPK2, and characterized its function in defense against Rhizoctonia solani causing stem canker in potato. RESULTS: Expressions of both StCBL4 and StCIPK2 from potato were coordinately induced upon R. solani infection and following exposure to the defense genes. Furthermore, transient overexpression of StCBL4 and StCIPK2 individually and synergistically increased the tolerance of potato plants to R. solani in Nicotiana benthamiana. Additionally, the transgenic potato has also been shown to enhance resistance significantly. In contrast, susceptibility to R. solani was exhibited in N. benthamiana following virus-induced gene silencing of NbCBL and NbCIPK2. Evidence revealed that StCBL4 could interact in yeast and in planta with StCIPK2. StCBL4 and StCIPK2 transcription was induced upon R. solani infection and this expression in response to the pathogen was enhanced in StCBL4- and StCIPK2-transgenic potato. Moreover, accumulated expression of pathogenesis-related (PR) genes and reactive oxygen species (ROS) was significantly upregulated and enhanced in both StCBL4- and StCIPK2- transgenic potato. DISCUSSION: Accordingly, StCBL4 and StCIPK2 were involved in regulating the immune response to defend the potato plant against R. solani. Together, our data demonstrate that StCBL4 functions in concert with StCIPK2, as positive regulators of immunity, contributing to combating stem canker disease in potato. Frontiers Media S.A. 2023-01-04 /pmc/articles/PMC9845770/ /pubmed/36687567 http://dx.doi.org/10.3389/fmicb.2022.1032900 Text en Copyright © 2023 Yang, Li, Lu, Wang, Min, Guo, Wei, Wang, Dong, Mao, Hu and Wang. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Yang, Shuai
Li, Jie
Lu, Jie
Wang, Ling
Min, Fanxiang
Guo, Mei
Wei, Qi
Wang, Wenzhong
Dong, Xuezhi
Mao, Yanzhi
Hu, Linshuang
Wang, Xiaodan
Potato calcineurin B-like protein CBL4, interacting with calcineurin B-like protein-interacting protein kinase CIPK2, positively regulates plant resistance to stem canker caused by Rhizoctonia solani
title Potato calcineurin B-like protein CBL4, interacting with calcineurin B-like protein-interacting protein kinase CIPK2, positively regulates plant resistance to stem canker caused by Rhizoctonia solani
title_full Potato calcineurin B-like protein CBL4, interacting with calcineurin B-like protein-interacting protein kinase CIPK2, positively regulates plant resistance to stem canker caused by Rhizoctonia solani
title_fullStr Potato calcineurin B-like protein CBL4, interacting with calcineurin B-like protein-interacting protein kinase CIPK2, positively regulates plant resistance to stem canker caused by Rhizoctonia solani
title_full_unstemmed Potato calcineurin B-like protein CBL4, interacting with calcineurin B-like protein-interacting protein kinase CIPK2, positively regulates plant resistance to stem canker caused by Rhizoctonia solani
title_short Potato calcineurin B-like protein CBL4, interacting with calcineurin B-like protein-interacting protein kinase CIPK2, positively regulates plant resistance to stem canker caused by Rhizoctonia solani
title_sort potato calcineurin b-like protein cbl4, interacting with calcineurin b-like protein-interacting protein kinase cipk2, positively regulates plant resistance to stem canker caused by rhizoctonia solani
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9845770/
https://www.ncbi.nlm.nih.gov/pubmed/36687567
http://dx.doi.org/10.3389/fmicb.2022.1032900
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