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葡萄 VvNPR1.1 是 AtNPR1 的功能同源物,其在葡萄中的过表达触发了 PR 基因的组成性激活,并增强了对白粉病的抗性。

Vitis vinifera VvNPR1.1 is the functional ortholog of AtNPR1 and its overexpression in grapevine triggers constitutive activation of PR genes and enhanced resistance to powdery mildew.

机构信息

Université de Haute Alsace, Laboratoire Vigne, Biotechnologies et Environnement (EA3991), 33 rue de Herrlisheim, 68000, Colmar, France.

出版信息

Planta. 2011 Aug;234(2):405-17. doi: 10.1007/s00425-011-1412-1. Epub 2011 Apr 20.

DOI:10.1007/s00425-011-1412-1
PMID:21505863
Abstract

Studying grapevine (Vitis vinifera) innate defense mechanisms is a prerequisite to the development of new protection strategies, based on the stimulation of plant signaling pathways to trigger pathogen resistance. Two transcriptional coactivators (VvNPR1.1 and VvNPR1.2) with similarity to Arabidopsis thaliana NPR1 (Non-Expressor of PR genes 1), a well-characterized and key signaling element of the salicylic acid (SA) pathway, were recently isolated in Vitis vinifera. In this study, functional characterization of VvNPR1.1 and VvNPR1.2, including complementation of the Arabidopsis npr1 mutant, revealed that VvNPR1.1 is a functional ortholog of AtNPR1, whereas VvNPR1.2 likely has a different function. Ectopic overexpression of VvNPR1.1 in the Arabidopsis npr1-2 mutant restored plant growth at a high SA concentration, Pathogenesis Related 1 (PR1) gene expression after treatment with SA or bacterial inoculation, and resistance to virulent Pseudomonas syringae pv. maculicola bacteria. Moreover, stable overexpression of VvNPR1.1-GFP in V. vinifera resulted in constitutive nuclear localization of the fusion protein and enhanced PR gene expression in uninfected plants. Furthermore, grapevine plants overexpressing VvNPR1.1-GFP exhibited an enhanced resistance to powdery mildew infection. This work highlights the importance of the conserved SA/NPR1 signaling pathway for resistance to biotrophic pathogens in V. vinifera.

摘要

研究葡萄(Vitis vinifera)先天防御机制是开发基于刺激植物信号通路触发病原体抗性的新保护策略的前提。两个与拟南芥 NPR1(非表达 PR 基因 1)具有相似性的转录共激活因子(VvNPR1.1 和 VvNPR1.2)最近在葡萄中被分离出来,NPR1 是水杨酸(SA)途径的一个特征明显且关键的信号元件。在本研究中,对 VvNPR1.1 和 VvNPR1.2 的功能进行了表征,包括对拟南芥 npr1 突变体的互补性,结果表明 VvNPR1.1 是 AtNPR1 的功能同源物,而 VvNPR1.2 可能具有不同的功能。在拟南芥 npr1-2 突变体中异位过表达 VvNPR1.1 恢复了植物在高 SA 浓度下的生长,SA 处理或细菌接种后 PR1 基因的表达,以及对强毒丁香假单胞菌 pv. maculicola 细菌的抗性。此外,V. vinifera 中 VvNPR1.1-GFP 的稳定过表达导致融合蛋白的组成型核定位和未感染植物中 PR 基因表达的增强。此外,过表达 VvNPR1.1-GFP 的葡萄植物对白粉病感染表现出增强的抗性。这项工作强调了保守的 SA/NPR1 信号通路对葡萄中生物营养性病原体抗性的重要性。

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