Department of Plant Pathology, College of Agricultural and Environmental Sciences, University of California, Davis, CA 95616, USA.
Virology. 2011 Aug 15;417(1):71-8. doi: 10.1016/j.virol.2011.04.022. Epub 2011 Jun 2.
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.
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。