Siddell S G, Smith A E
J Virol. 1978 Aug;27(2):427-31. doi: 10.1128/JVI.27.2.427-431.1978.
Polyoma virus mRNA, isolated from the cytoplasm of 3T6 cells late after infection and purified by hybridization to HpaII fragment 3 of polyoma virus DNA, was separated on 50% formamide-containing sucrose density gradients, and the fractionated RNA was recovered and translated in vitro. Analysis of the cell-free products showed that the minor virion protein VP3 was synthesized from an mRNA sedimenting at approximately 18S betweeen the 19S VP2 mRN and the 16S VP1 mRNA. Other experiments showed that the VP2 and VP3 can be labeled with formyl methionine from initiator tRNA. We conclude that there are three late polyoma virus mRNA's, each directing the synthesis of only one viral capsid protein.
从感染后期的3T6细胞胞质中分离出的多瘤病毒mRNA,通过与多瘤病毒DNA的HpaII片段3杂交进行纯化,在含50%甲酰胺的蔗糖密度梯度上进行分离,回收分级分离的RNA并在体外进行翻译。对无细胞产物的分析表明,次要病毒粒子蛋白VP3是由一种mRNA合成的,该mRNA在19S VP2 mRNA和16S VP1 mRNA之间沉降约18S。其他实验表明,VP2和VP3可以用起始tRNA上的甲酰甲硫氨酸进行标记。我们得出结论,有三种晚期多瘤病毒mRNA,每种都仅指导一种病毒衣壳蛋白的合成。