PoWRKY69‐PoVQ11 module positively regulates drought tolerance by accumulating fructose in Paeonia ostii

WRKY蛋白质结构域 双分子荧光互补 生物 转录因子 调节器 基因沉默 非生物胁迫 RNA干扰 生物化学 细胞生物学 基因表达 基因 转录组 核糖核酸
作者
Yuting Luan,Zijie Chen,Ziwen Fang,Jiasong Meng,Jun Tao,Daqiu Zhao
出处
期刊:Plant Journal [Wiley]
卷期号:119 (4): 1782-1799 被引量:13
标识
DOI:10.1111/tpj.16884
摘要

SUMMARY Drought is a detrimental environmental factor that restricts plant growth and threatens food security throughout the world. WRKY transcription factors play vital roles in abiotic stress response. However, the roles of IIe subgroup members from WRKY transcription factor family in soluble sugar mediated drought response are largely elusive. In this study, we identified a drought‐responsive IIe subgroup WRKY transcription factor, PoWRKY69, from Paeonia ostii . PoWRKY69 functioned as a positive regulator in response to drought stress with nucleus expression and transcriptional activation activity. Silencing of PoWRKY69 increased plants sensitivity to drought stress, whereas conversely, overexpression of PoWRKY69 enhanced drought tolerance in plants. As revealed by yeast one‐hybrid, electrophoretic mobility shift assay, and luciferase reporter assays, PoWRKY69 could directly bind to the W‐box element of fructose‐1,6‐bisphosphate aldolase 5 ( PoFBA5 ) promoter, contributing to a cascade regulatory network to activate PoFBA5 expression. Furthermore, virus‐induced gene silencing and overexpression assays demonstrated that PoFBA5 functioned positively in response to drought stress by accumulating fructose to alleviate membrane lipid peroxidation and activate antioxidant defense system, these changes resulted in reactive oxygen species scavenging. According to yeast two‐hybrid, bimolecular fluorescence complementation, and firefly luciferase complementation imaging assays, valine‐glutamine 11 (PoVQ11) physically interacted with PoWRKY69 and led to an enhanced activation of PoWRKY69 on PoFBA5 promoter activity. This study broadens our understanding of WRKY69‐VQ11 module regulated fructose accumulation in response to drought stress and provides feasible molecular measures to create novel drought‐tolerant germplasm of P. ostii .
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