Pawson T, Martin G S, Smith A E
J Virol. 1976 Sep;19(3):950-67. doi: 10.1128/JVI.19.3.950-967.1976.
Nondefective and transformation-defective virion subunit RNAs from two strains of Rous sarcoma virus (RSV) were translated in cell-free systems derived from Krebs IIA ascites cells, wheat germ, and L-cells. In each case the predominant viral-specific product was a polypeptide of molecular weight 76,000 that is related to the internal viral group-specific antigens, as judged by immunoprecipitation with monospecific antisera and tryptic peptide fingerprinting. No difference could be detected between the translation products of 35S RNA from nondefective and transformation-defective RSV virions, nor of 35S RNA from different strains of RSV. The 76,000-molecular-weight polypeptide synthesized in response to 35S RNA in vitro was labeled with formyl-methionine from initiator tRNA. Models for viral protein synthesis are discussed in the light of these results, and arguments positioning the group-specific antigen gene at the 5' end of the 35S RNA are presented.
来自两株劳氏肉瘤病毒(RSV)的无缺陷和转化缺陷病毒粒子亚基RNA,在源自克雷布斯IIA腹水细胞、小麦胚芽和L细胞的无细胞系统中进行了翻译。在每种情况下,主要的病毒特异性产物都是一种分子量为76,000的多肽,通过用单特异性抗血清进行免疫沉淀和胰蛋白酶肽指纹图谱分析判断,该多肽与病毒内部群特异性抗原相关。在无缺陷和转化缺陷的RSV病毒粒子的35S RNA的翻译产物之间,以及不同株RSV的35S RNA的翻译产物之间,均未检测到差异。体外响应35S RNA合成的分子量为76,000的多肽,用起始tRNA的甲酰甲硫氨酸进行了标记。根据这些结果讨论了病毒蛋白质合成的模型,并提出了将群特异性抗原基因定位在35S RNA 5'端的论据。