Nicolas O, Dunnington S W, Gotow L F, Pirone T P, Hellmann G M
Bowman Gray Technical Center, R. J. Reynolds Tobacco Company, Winston-Salem, North Carolina 27102, USA.
Virology. 1997 Oct 27;237(2):452-9. doi: 10.1006/viro.1997.8780.
The va gene is used in commercial Burley tobacco cultivars including cv TN 86 to confer resistance to tobacco vein mottling virus (TVMV) and, to some extent, other potyviruses. A naturally occurring strain of TVMV (TVMV-S), which overcomes this resistance, was isolated from TN 86 plants. To investigate the mechanism by which TVMV-S overcomes va gene resistance, a cDNA clone encompassing the complete genome of TVMV-S was produced. Using chimeric transcripts combining regions of TVMV-S and regions of the wild-type strain (TVMV-WT) to which TN 86 is resistant, it was demonstrated that a domain within the VPg protein is responsible for overcoming va resistance in TN 86. DNA sequence analysis revealed six amino acid differences between the two strains of TVMV within this domain. Inclusion of sequences for four of the TVMV-S VPg amino acids was sufficient to confer the resistance-overcoming phenotype to all corresponding transcripts. Coinoculation experiments suggested that the resistance of TN 86 to TVMV-WT was not due to the induction of a general host defense response. The results are compatible with the hypothesis that VPg must assume an appropriate configuration in order to interact with appropriate host components and facilitate systemic virus movement.
va基因用于包括TN 86品种在内的商业白肋烟品种中,以赋予对烟草脉斑驳病毒(TVMV)以及在一定程度上对其他马铃薯Y病毒属病毒的抗性。从TN 86植株中分离出一种能克服这种抗性的天然TVMV毒株(TVMV-S)。为了研究TVMV-S克服va基因抗性的机制,构建了一个包含TVMV-S完整基因组的cDNA克隆。通过使用结合TVMV-S区域和TN 86所抗性的野生型毒株(TVMV-WT)区域的嵌合转录本,证明VPg蛋白内的一个结构域负责克服TN 86中的va抗性。DNA序列分析揭示了这两种TVMV毒株在该结构域内有六个氨基酸差异。包含TVMV-S VPg四个氨基酸的序列足以赋予所有相应转录本克服抗性的表型。共接种实验表明,TN 86对TVMV-WT的抗性并非由于诱导了一般的宿主防御反应。这些结果与以下假设相符:VPg必须呈现适当的构象,以便与适当的宿主成分相互作用并促进病毒的系统移动。