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首页> 外文期刊>African Journal of Biotechnology >Identification and expression analysis of a pathogen-responsive PR-1 gene from Chinese wild Vitis quinquangularis
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Identification and expression analysis of a pathogen-responsive PR-1 gene from Chinese wild Vitis quinquangularis

机译:中国野生五瓣葡萄病原体反应性PR-1基因的鉴定与表达分析

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摘要

In response to pathogen attacks, plant produces a wide range of pathogenesis-related (PR) proteins.?PR-1 genes represent the first identified PR gene family. Most members of PR-1 gene family are not inducible by pathogen attacks.?In this study, we identified a pathogen-responsive PR-1 gene designated as?VqPR-1?(GenBank accession no. JN256202), in a subtractive suppression hybridization (SSH) cDNA-library from?Elsinoe ampelina-inoculated young leaves of Chinese wild?Vitis quinquangularis?clone ‘shang-24’.?VqPR-1?protein contained the requisite signal sequence at the N-terminus, a conserved three-dimensional structure called ‘PR-1 fold’ and a highly conserved six-cysteine motif. Expression level of?VqPR-1?rose rapidly in response to?E. ampelina?infection. The three tested plant defence signaling molecules, salicylic acid (SA), ethephon (Eth) and methyl jasmonate (MeJA) all triggered an induction of?VqPR-1. However, the induction by addition of MeJA was weaker than that induced by SA and Eth. In addition, the response to inoculation withE. ampelina?or treatment with signaling molecules, was sometimes a suppression ofVqPR-1?gene expression. The highest expression of?VqPR-1?was observed in flowers, stems and leaves, while low-level or no obvious transcripts were detected in pericarps and tendrils, respectively.
机译:作为对病原体侵袭的响应,植物产生各种与病程相关的(PR)蛋白。?PR-1基因代表第一个鉴定出的PR基因家族。 PR-1基因家族的大多数成员不能被病原体攻击诱导。在这项研究中,我们通过消减抑制杂交鉴定了一种病原体应答性PR-1基因,命名为“ VqPR-1”(GenBank登录号JN256202)。 (SSH)cDNA文库,来自中国产的野生拟南芥葡萄(Quans Quangularularis)克隆'shang-24'的幼叶中分离出的?qq-1蛋白质在N末端包含一个必需的信号序列,这是一个保守的三维结构称为“ PR-1折叠”和高度保守的六个半胱氨酸基序。响应于ΔE,ΔVqPR-1的表达水平迅速上升。 ampelina?感染。三种受试植物防御信号分子水杨酸(SA),乙烯利(Eth)和茉莉酸甲酯(MeJA)均诱发了αVqPR-1的诱导。但是,添加MeJA的诱导作用比SA和Eth诱导的作用弱。另外,接种E的反应。或用信号分子处理有时会抑制VqPR-1α基因的表达。在花,茎和叶中观察到最高的“ VqPR-1”表达,而在果皮和卷须中分别检测到低水平或没有明显的转录本。

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