Gallione C J, Rose J K
J Virol. 1985 May;54(2):374-82. doi: 10.1128/JVI.54.2.374-382.1985.
DNA sequences were determined for three cDNA clones encoding vesicular stomatitis virus glycoproteins from the tsO45 mutant (which encodes a glycoprotein that exhibits temperature-sensitive cell-surface transport), the wild-type parent strain, and a spontaneous revertant of tsO45. The DNA sequence analysis showed that as many as three amino acid changes could be responsible for the transport defect. By recombining the cDNA clones in vitro and expressing the recombinants in COS cells, we were able to trace the critical lesion in tsO45 to a single substitution of a polar amino acid (serine) for a hydrophobic amino acid (phenylalanine) in a hydrophobic domain. We suggest that this nonconservative substitution may block protein transport by causing protein denaturation at the nonpermissive temperature. Comparison of the predicted glycoprotein sequences from two vesicular stomatitis virus strains suggests a possible basis for the differential carbohydrate requirement in transport of the two glycoproteins.
测定了来自tsO45突变体(其编码一种表现出温度敏感型细胞表面转运的糖蛋白)、野生型亲本菌株以及tsO45的自发回复突变体的三个编码水泡性口炎病毒糖蛋白的cDNA克隆的DNA序列。DNA序列分析表明,多达三个氨基酸变化可能导致转运缺陷。通过在体外重组cDNA克隆并在COS细胞中表达重组体,我们能够将tsO45中的关键损伤追溯到疏水结构域中一个极性氨基酸(丝氨酸)被一个疏水氨基酸(苯丙氨酸)的单一代替。我们认为这种非保守性替代可能通过在非允许温度下导致蛋白质变性来阻断蛋白质转运。对两种水泡性口炎病毒株预测的糖蛋白序列的比较表明了两种糖蛋白在转运中对碳水化合物需求差异的可能基础。