Faras A J, Dahlberg J E, Sawyer R C, Harada F, Taylor J M, Levinson W E, Bishop J M, Goodman H M
J Virol. 1974 May;13(5):1134-42. doi: 10.1128/JVI.13.5.1134-1142.1974.
The 70S RNA of Rous sarcoma virus contains 4S RNAs which serve as primers for the initiation of DNA synthesis in vitro by the RNA-directed DNA polymerase of the virus. We purified these primers in three different ways-by isolation of the covalent complex between primer and nascent DNA, by differential melting of the 70S RNA, and by two-dimensional electrophoresis in polyacrylamide gels. The 4S RNAs purified by these procedures were homogeneous and possessed very similar if not identical nucleotide compositions and sequences. The RNAs were approximately 75 nucleotides long, had pG at the 5' terminus and CpCpA(OH) at the 3' terminus, and contained a number of minor nucleotides characteristic of tRNA. In contrast to most tRNA's, the primer lacked rTp and contained Gp (Psip, Psip, Cp) Gp (possibly in place of the characteristic sequence GprTpPsipCpGp). At least 50% of the 4S primers available on 70S RNA were utilized in a standard polymerase reaction in vitro.
劳氏肉瘤病毒的70S RNA含有4S RNA,这些4S RNA在体外可作为该病毒的RNA指导的DNA聚合酶启动DNA合成的引物。我们通过三种不同的方法纯化这些引物——通过分离引物与新生DNA之间的共价复合物、通过70S RNA的差异解链以及通过聚丙烯酰胺凝胶二维电泳。通过这些程序纯化的4S RNA是均一的,并且具有非常相似(如果不是完全相同)的核苷酸组成和序列。这些RNA大约75个核苷酸长,5'末端为pG,3'末端为CpCpA(OH),并且含有一些tRNA特有的稀有核苷酸。与大多数tRNA不同,引物缺乏rTp并含有Gp(ψp、ψp、Cp)Gp(可能取代了特征序列GprTpψpCpGp)。70S RNA上至少50%的4S引物可用于体外标准聚合酶反应。