White B T, McGeoch D J
MRC Virology Unit, University of Glasgow, U.K.
J Gen Virol. 1987 Dec;68 ( Pt 12):3033-44. doi: 10.1099/0022-1317-68-12-3033.
We describe the isolation and characterization of conditional lethal amber nonsense mutants of vesicular stomatitis virus (VSV), Indiana serotype. The mutants were isolated from a chemically mutagenized stock of wild-type virus by their ability to grow on genetically engineered cells which express a Xenopus laevis amber suppressor tyrosine tRNA gene (su+ cells) but not on the non-suppressor parental cells (su- cells). Five mutations were assigned to complementation group I (the L gene) and one to complementation group V (the G gene) by complementation analysis using temperature-sensitive mutants representing each of the five VSV cistrons. Four of the group I mutants were observed to synthesize a novel polypeptide species in su+ cells. Immunoprecipitation and immunoblotting studies using monospecific antisera directed against the N and C termini of the VSV L protein showed that the novel polypeptide species contain N terminal- but not C terminal-specific sequences and can thus be considered to be truncated versions of the L protein. In addition a protein which again contained N terminal- but not C terminal-specific sequences could be identified for the fifth group I mutant. Revertants of four of the group I mutants were isolated on the su- cells. The revertants all synthesized normal L protein but not the putative truncated version.
我们描述了水疱性口炎病毒(VSV)印第安纳血清型条件致死性琥珀色无义突变体的分离和特性。这些突变体是从经化学诱变的野生型病毒株中分离出来的,其依据是它们能够在表达非洲爪蟾琥珀色抑制酪氨酸tRNA基因的基因工程细胞(su +细胞)上生长,而不能在非抑制性亲代细胞(su-细胞)上生长。通过使用代表VSV五个顺反子的温度敏感突变体进行互补分析,五个突变被归为互补组I(L基因),一个突变归为互补组V(G基因)。观察到互补组I中的四个突变体在su +细胞中合成了一种新的多肽。使用针对VSV L蛋白N端和C端的单特异性抗血清进行免疫沉淀和免疫印迹研究表明,这种新的多肽含有N端特异性序列,但不含有C端特异性序列,因此可以认为是L蛋白的截短形式。此外,对于第五个互补组I突变体,可以鉴定出一种同样含有N端特异性序列但不含有C端特异性序列的蛋白质。在su-细胞上分离出了互补组I中四个突变体的回复突变体。这些回复突变体都合成了正常的L蛋白,而不是推定的截短形式。