Schubert M, Harmison G G, Richardson C D, Meier E
Proc Natl Acad Sci U S A. 1985 Dec;82(23):7984-8. doi: 10.1073/pnas.82.23.7984.
The large gene, L, of vesicular stomatitis virus (VSV), which codes for the multifunctional RNA-dependent RNA polymerase, was assembled from five overlapping cDNA clones. The sequence of the 6.4-kilobase gene of the final construct was identical to the consensus sequence reported earlier. The gene was inserted into the simian virus 40 transient expression vector pJC119. Antibodies directed against synthetic peptides corresponding to the amino and carboxyl termini of the L protein were raised in rabbits. Both antibodies specifically immunostained the cytoplasm of COS cells that had been transfected with the vector DNA. The expressed L protein was immunoprecipitated from cell extracts and it was identical in size to the L protein of the virion (241 kilodaltons). Most importantly, COS cells that expressed the recombinant L protein transcribed, replicated, and consequently complemented and rescued temperature-sensitive RNA polymerase mutants of VSV at the nonpermissive temperature. The kinetics of virus release were similar to those of a wild-type VSV infection. We conclude that the recombinant RNA polymerase protein L is indistinguishable in its size and its functions from the VSV polymerase.
水泡性口炎病毒(VSV)的大基因L编码多功能RNA依赖性RNA聚合酶,它由五个重叠的cDNA克隆组装而成。最终构建体的6.4千碱基基因序列与先前报道的共有序列相同。该基因被插入到猿猴病毒40瞬时表达载体pJC119中。针对与L蛋白氨基和羧基末端相对应的合成肽的抗体在兔子体内产生。两种抗体都特异性地免疫染色了用载体DNA转染的COS细胞的细胞质。从细胞提取物中免疫沉淀出表达的L蛋白,其大小与病毒体的L蛋白(241千道尔顿)相同。最重要的是,表达重组L蛋白的COS细胞在非允许温度下转录、复制,从而互补并拯救了VSV的温度敏感型RNA聚合酶突变体。病毒释放的动力学与野生型VSV感染相似。我们得出结论,重组RNA聚合酶蛋白L在大小和功能上与VSV聚合酶没有区别。