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来自海岛棉的一个Ve同源基因Gbvdr3增强了对大丽轮枝菌的防御反应。

A Ve homologous gene from Gossypium barbadense, Gbvdr3, enhances the defense response against Verticillium dahliae.

作者信息

Chen Tianzi, Kan Jialiang, Yang Yuwen, Ling Xitie, Chang Youhong, Zhang Baolong

机构信息

Provincial Key Laboratory of Agrobiology, Jiangsu Academy of Agricultural Sciences, Nanjing 210014, China.

Provincial Key Laboratory of Agrobiology, Jiangsu Academy of Agricultural Sciences, Nanjing 210014, China.

出版信息

Plant Physiol Biochem. 2016 Jan;98:101-11. doi: 10.1016/j.plaphy.2015.11.015. Epub 2015 Nov 24.

DOI:10.1016/j.plaphy.2015.11.015
PMID:26686282
Abstract

The tomato Ve1 gene and several Ve1 homologues are involved in the resistance to Verticillium dahliae. Here, we report on another Ve homologous gene, Gbvdr3, from a Verticillium wilt-resistant cotton cultivar, Gossypium barbadense Hai7124, which has a 3207-bp region that encodes a predicted receptor-like protein. Transient expression analyses indicated that Gbvdr3 is localized in the plasma membrane, and virus-induced gene silencing of Gbvdr3 compromised the resistance of Hai7124 cotton to a defoliating strain of V. dahliae, V991, but not to a non-defoliating strain, BP2. This resistance pattern was further confirmed by over-expression of Gbvdr3 in transgenic Arabidopsis, which significantly elevated the expression of the ethylene-regulated gene GST2, the ethylene- and jasmonic acid-regulated defense-related genes PR3 and PDF1.2, and the salicylic acid-regulated genes PR1 and PR5, but not the PR2 gene. It also triggered the accumulation of hydrogen peroxide and callose at early time points during infection by the V991 defoliating strain. In contrast, elevated accumulation of hydrogen peroxide or callose in Gbvdr3-expressed Arabidopsis leaves was not apparent under infection by the non-defoliating strain, BP2. These results suggested that Gbvdr3 is involved in the resistance to a unique spectrum of defoliating V. dahliae strains.

摘要

番茄Ve1基因和几个Ve1同源基因参与对大丽轮枝菌的抗性。在此,我们报道了另一个来自抗黄萎病棉花品种海岛棉海7124的Ve同源基因Gbvdr3,它有一个3207 bp的区域,编码一个预测的类受体蛋白。瞬时表达分析表明,Gbvdr3定位于质膜,对Gbvdr3进行病毒诱导的基因沉默会削弱海7124棉花对大丽轮枝菌落叶菌株V991的抗性,但不会削弱对非落叶菌株BP2的抗性。在转基因拟南芥中过表达Gbvdr3进一步证实了这种抗性模式,它显著提高了乙烯调节基因GST2、乙烯和茉莉酸调节的防御相关基因PR3和PDF1.2以及水杨酸调节基因PR1和PR5的表达,但没有提高PR2基因的表达。它还在V991落叶菌株感染的早期阶段引发了过氧化氢和胼胝质的积累。相比之下,在非落叶菌株BP2感染下,Gbvdr3表达的拟南芥叶片中过氧化氢或胼胝质的积累增加并不明显。这些结果表明,Gbvdr3参与了对特定落叶大丽轮枝菌菌株谱的抗性。

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