Open AccessThe transcription factors VaERF16 and VaMYB306 interact to enhance resistance of grapevine to Botrytis cinerea infection
Author(s) -
Zhu Yanxun,
Zhang Xiuming,
Zhang Qihan,
Chai Shengyue,
Yin Wuchen,
Gao Min,
Li Zhi,
Wang Xiping
Publication year - 2022
Publication title -
molecular plant pathology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.945
H-Index - 103
eISSN - 1364-3703
pISSN - 1464-6722
DOI - 10.1111/mpp.13223
Subject(s) - botrytis cinerea , biology , methyl jasmonate , bimolecular fluorescence complementation , jasmonate , complementation , pseudomonas syringae , transcription factor , jasmonic acid , promoter , gene , actinidia , arabidopsis , genetics , botany , gene expression , mutant
Botrytis cinerea is a fungus that infects cultivated grape ( Vitis vinifera ); the identification and characterization of resistance mechanisms in the host is of great importance for the grape industry. Here, we report that a transcription factor in the ethylene‐responsive factor (ERF) family ( VaERF16 ) from Chinese wild grape ( Vitis amurensis ‘Shuang You’) is expressed during B . cinerea infection and in response to treatments with the hormones ethylene and methyl jasmonate. Heterologous overexpression of VaERF16 in Arabidopsis thaliana substantially enhanced resistance to B . cinerea and the bacterium Pseudomonas syringae DC3000 via the salicylic acid and jasmonate/ethylene signalling pathways. Yeast two‐hybrid, bimolecular fluorescence complementation, and co‐immunoprecipitation assays indicated that VaERF16 interacts with the MYB family transcription factor VaMYB306. Overexpression of VaERF16 or VaMYB306 in grape leaves increased resistance to B . cinerea and caused an up‐regulation of the defence‐related gene PDF1.2 , which encodes a defensin‐like protein. Conversely, silencing of either gene resulted in increased susceptibility to B. cinerea . Yeast one‐hybrid and dual‐luciferase assays indicated that VaERF16 increased the transcript levels of VaPDF1.2 by binding directly to the GCC box in its promoter. Notably, VaMYB306 alone did not bind to the VaPDF1.2 promoter, but the VaERF16–VaMYB306 transcriptional complex resulted in higher transcript levels of VaPDF1.2 , suggesting that the proteins function through their mutual interaction. Elucidation of this regulatory module may be of value in enhancing resistance of grapevine to B. cinerea infection.