Sefton B M, Beemon K, Hunter T
J Virol. 1978 Dec;28(3):957-71. doi: 10.1128/JVI.28.3.957-971.1978.
We have compared the polypeptide products of the src gene of several strains of Rous sarcoma virus produced by in vitro translation of heat-denatured 70S virion RNA in the nuclease-treated reticulocyte lysate with those present in chick cells transformed by these viruses. We have done this by immunoprecipitation, using sera from rabbits injected at birth with Schmidt-Ruppin Rous sarcoma virus. In vitro translation results in the synthesis of at least nine polypeptides which appear to be encoded by the src gene. These range in size from 17,000 to 60,000 daltons. The sera from tumor-bearing rabbits precipitated these polypeptides arising from the in vitro translation of RNA from Schmidt-Ruppin Rous sarcoma virus of both subgroup A and subgroup D and from one stock of Prague Rous sarcoma virus of subgroup C. In each case, all of this family of related polypeptides could be precipitated except the smallest, the 17,000-dalton polypeptide. No precipitation of analogous polypeptides resulting from the translation of RNA from other strains of Rous sarcoma virus was observed. Cells transformed by these three strains of Rous sarcoma virus contain easily detectable amounts of a polypeptide, p60src, essentially identical to the 60,000-dalton in vitro product. With one exception, they do not contain significant amounts of polypeptides analogous to the smaller in vitro products which can be precipitated by these sera. Cells transformed by one stock of Schmidt-Ruppin Rous sarcoma virus of subgroup A did contain a 39,000-dalton polypeptide, which was related, by peptide mapping, to the 60,000-dalton polypeptide and was similar in size to a precipitable in vitro product. The 60,000-dalton polypeptide present in transformed cells appeared to be phosphorylated 10 to 25 min after its synthesis, metabolically very stable, and not derived from a precursor polypeptide. All immunoprecipitates from transformed cells which contained p60src also contained an 80,000-dalton phosphoprotein. This polypeptide is unrelated to p60src, as determined by peptide mapping, and may well be a host cell polypeptide which is specifically associated with p60src.
我们将经核酸酶处理的网织红细胞裂解物中热变性的70S病毒粒子RNA体外翻译产生的几种劳氏肉瘤病毒株src基因的多肽产物,与这些病毒转化的鸡细胞中存在的多肽产物进行了比较。我们通过免疫沉淀法做到了这一点,所用血清来自出生时注射施密特-鲁平氏劳氏肉瘤病毒的兔子。体外翻译导致至少九种多肽的合成,这些多肽似乎由src基因编码。其大小范围从17,000到60,000道尔顿。荷瘤兔子的血清沉淀了来自A亚组和D亚组的施密特-鲁平氏劳氏肉瘤病毒以及C亚组的一批布拉格劳氏肉瘤病毒RNA体外翻译产生的这些多肽。在每种情况下,除了最小的17,000道尔顿多肽外,这个相关多肽家族的所有成员都能被沉淀。未观察到其他劳氏肉瘤病毒株RNA翻译产生的类似多肽的沉淀。这三种劳氏肉瘤病毒株转化的细胞含有易于检测到的一种多肽p60src,它与60,000道尔顿的体外产物基本相同。除了一个例外,它们不含大量类似于这些血清可沉淀的较小体外产物的多肽。A亚组的一批施密特-鲁平氏劳氏肉瘤病毒转化的细胞确实含有一种39,000道尔顿的多肽,通过肽图谱分析,它与60,000道尔顿的多肽相关,并且大小与一种可沉淀的体外产物相似。转化细胞中存在的60,000道尔顿多肽在合成后10至25分钟似乎被磷酸化,代谢上非常稳定,且不是来自前体多肽。来自含有p60src的转化细胞的所有免疫沉淀物还含有一种80,000道尔顿的磷蛋白。通过肽图谱分析确定,该多肽与p60src无关,很可能是一种与p60src特异性相关的宿主细胞多肽。