Lewis J B, Atkins J F, Baum P R, Solem R, Gesteland R F, Anderson C W
Cell. 1976 Jan;7(1):141-51. doi: 10.1016/0092-8674(76)90264-6.
Virus-specific RNA was prepared from cells early after adenovirus type 2 infection and fractionated by hybridization to specific fragments of viral DNA. The viral mRNA was used to program cell-free protein synthesis, and the products were analyzed by electrophoresis. The genes for the early polypeptides of apparent molecular weight 44,000, 15,000, 72,000, 15,500, 19,000, and 11,000 daltons were located, respectively, between positions 0-4.1, 4.1-16.7, 58.5-70.7, 75.9-83.4, 89.7-98.6, and 89.7-98.6 of the conventional adenovirus DNA map. The polypeptide of molecular weight 72,000 daltons was shown to be the single-stranded DNA-binding protein described by others. RNAs from three different adeno-transformed cell lines each program the synthesis in vitro of predominantly the 15K polypeptide, as well as variable amounts of the polypeptide of molecular weight 44,000 daltons. The genes for these two polypeptides are located in the portion of DNA known to be required for transformation of rodent cells by adenovirus.
在腺病毒2型感染后早期,从细胞中制备病毒特异性RNA,并通过与病毒DNA的特定片段杂交进行分级分离。病毒mRNA用于无细胞蛋白质合成程序,产物通过电泳进行分析。表观分子量为44,000、15,000、72,000、15,500、19,000和11,000道尔顿的早期多肽基因,分别位于传统腺病毒DNA图谱的0 - 4.1、4.1 - 16.7、58.5 - 70.7、75.9 - 83.4、89.7 - 98.6和89.7 - 98.6位置之间。分子量为72,000道尔顿的多肽被证明是其他人描述的单链DNA结合蛋白。来自三种不同腺病毒转化细胞系的RNA,每种都在体外主要指导15K多肽以及不同量的分子量为44,000道尔顿的多肽的合成。这两种多肽的基因位于已知腺病毒转化啮齿动物细胞所需的DNA部分。