南美超级胎牛血清999尝鲜特惠
转染试剂低至5折
基质胶阶梯特惠
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南美超级胎牛血清999尝鲜特惠
转染试剂低至5折
基质胶阶梯特惠
积分商城,好礼送不停
分子生物学
IVD分子诊断
细胞培养与分析
蛋白研究
细胞因子
重组蛋白
抗体
高通量测序建库
病原检测UCF系列
生物医药
工具酶
抑制剂激活剂与常用试剂
仪器
耗材

VvWRKY37通过ABA介导的信号通路调控葡萄芽萌发的分子机制研究

The VvWRKY37 Regulates Bud Break in Grape Vine Through ABA-Mediated Signaling Pathways

Feng-Pan Wang, Pan-Pan Zhao, Lei Zhang, Heng Zhai, Muhammad Abid, Yuan-Peng Du

Journal:Frontiers in Plant Science

IF:6.63

DOI:10.3389/fpls.2022.929892

PMID:35783936

Published:2022-06-16

research field:神经科学分子生物学药理学精神病学

Abstract

Dormancy is a common survival strategy in plants to temporarily suspend visible growth under unsuitable conditions. The elaborate mechanism underlying bud break in perennial woody plants is gradually illustrated. Here, we identified a grape vine WRKY transcription factor, VvWRKY37 , which was highly expressed in dormant buds. It was particularly induced by the application of exogenous abscisic acid, and depressed on exposure to gibberellin and low temperature (4°C) stress at the transcript level. The yeast one-hybrid assay confirmed that VvWRKY37 had a transcriptional activity. Ectopic over-expression of VvWRKY37 significantly delayed bud break of transgenic poplar plants. As an ABA-inducible gene, VvWRKY37 also depressed the expression of ABA catabolic gene CYP707A s and enhanced the accumulation of endogenous ABA in transgenic poplar plants. The molecular pieces of evidence showed that VvWRKY37 preferentially recognized and bound W-box 5′-G/CATTGACT/C/G-3′ cis -element in vitro . Additionally, VvABI5 and VvABF2 acted as the upstream transcriptional activators of VvWRKY37 via protein-DNA interactions. Taken together, our findings provided valuable insights into a new regulatory mechanism of WRKY TF by which it modulates bud break through ABA-mediated signaling pathways.

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