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豇豆花叶病毒蛋白酶参与引发极端抗性。

Participation of the Cowpea mosaic virus protease in eliciting extreme resistance.

机构信息

Department of Plant Pathology, College of Agricultural and Environmental Sciences, University of California, Davis, CA 95616, USA.

出版信息

Virology. 2011 Aug 15;417(1):71-8. doi: 10.1016/j.virol.2011.04.022. Epub 2011 Jun 2.

Abstract

Extreme resistance of Arlington line cowpea (Vigna unguiculata) to Cowpea mosaic virus (CPMV) is under control of a dominant locus designated Cpa. We transiently expressed, using Tomato bushy stunt virus (TBSV) vectors and Agrobacterium tumefaciens, in nearly isogenic Cpa/Cpa and cpa/cpa cowpea lines, sequences from RNA1, the larger of two CPMV genomic RNAs. Activation of a Cpa-specific response mapped to the CPMV 24K protease (24KPro). Mutational analysis of the 24KPro gene implicated protease activity, rather than 24KPro structure, in Cpa-mediated recognition of CPMV invasion. A 24KPro with alanine replacing the active site cysteine [24KPro(C-A)], but not wildtype 24KPro, accumulated after agroinfiltration of the corresponding binary vector constructions into Cpa/Cpa cowpea. In cpa/cpa cowpea, both protease versions accumulated, with 24KPro(C-A) in greater abundance. Thus, enzymically active 24KPro was recognized by both cowpea genotypes, but in Cpa/Cpa cowpea the suppression of 24KPro accumulation was very strong, consistent with extreme resistance to CPMV.

摘要

阿灵顿线豇豆(Vigna unguiculata)对豇豆花叶病毒(CPMV)的极端抗性由一个显性基因座 Cpa 控制。我们使用番茄丛矮病毒(TBSV)载体和根癌农杆菌瞬时表达了近等基因 Cpa/Cpa 和 cpa/cpa 豇豆系中的 RNA1 序列,该序列是两个 CPMV 基因组 RNA 中的较大者。Cpa 特异性反应的激活被定位到 CPMV 24K 蛋白酶(24KPro)上。24KPro 基因的突变分析表明,在 Cpa 介导的 CPMV 入侵识别中,蛋白酶活性而非 24KPro 结构起作用。用丙氨酸取代活性位点半胱氨酸的 24KPro [24KPro(C-A)],但不是野生型 24KPro,在相应的二元载体构建物被农杆菌浸润到 Cpa/Cpa 豇豆中后积累。在 cpa/cpa 豇豆中,两种蛋白酶版本都积累了,24KPro(C-A)的丰度更高。因此,两种豇豆基因型都识别具有酶活性的 24KPro,但在 Cpa/Cpa 豇豆中,24KPro 积累的抑制非常强烈,与对 CPMV 的极端抗性一致。

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