Pettersson R F, Ambros V, Baltimore D
J Virol. 1978 Aug;27(2):357-65. doi: 10.1128/JVI.27.2.357-365.1978.
A protein similar to that previously demonstrated on poliovirus RNA and replicative intermediate RNA (VPg) was found on all sizes of nascent viral RNA molecules and on the polyuridylic acid isolated from negative-strand RNA. 32P-labeled nascent chains were released from their template RNA and fractionated by exclusion chromatography on agarose. Fingerprint analysis using two-dimensional polyacrylamide gels of RNase T1 oligonucleotides derived from nascent chains of different lengths showed that a size fractionation of nascent chains was achieved. VPg was recovered from nascent chains varying in length from 7,500 nucleotides (full-sized RNA) to about 500 nucleotides. No other type of 5' terminus could be demonstrated on nascent RNA, and the yield of VPg was consistent with one molecule of the protein on each nascent chain. These results are consistent with the concept that the protein is added to the 5' end of the growing RNA chains at a very early stage, possibly as a primer of RNA synthesis. Analysis of the polyuridylic acid tract isolated from the replicative intermediate and double-stranded RNAs indicated that a protein of the same size as that found on the nascent chains and virion RNA is also linked to the negative-strand RNAs. It is likely that a similar mechanism is responsible for initiation of synthesis of both plus- and minus-strand RNAs.
在所有大小的新生病毒RNA分子以及从负链RNA分离出的聚尿苷酸上,发现了一种与先前在脊髓灰质炎病毒RNA和复制中间体RNA(VPg)上所证实的蛋白质相似的蛋白质。用32P标记的新生链从其模板RNA上释放出来,并通过琼脂糖凝胶排阻色谱法进行分级分离。使用二维聚丙烯酰胺凝胶对来自不同长度新生链的核糖核酸酶T1寡核苷酸进行指纹分析,结果表明已实现了新生链的大小分级分离。从长度在7500个核苷酸(全长RNA)至约500个核苷酸不等的新生链中回收了VPg。在新生RNA上未发现其他类型的5'末端,并且VPg的产量与每条新生链上一个蛋白质分子的情况一致。这些结果与这样一种概念相符,即该蛋白质在很早的阶段就被添加到正在生长的RNA链的5'末端,可能作为RNA合成的引物。对从复制中间体和双链RNA中分离出的聚尿苷酸序列的分析表明,一种与在新生链和病毒体RNA上发现的大小相同的蛋白质也与负链RNA相连。很可能一种相似的机制负责正链和负链RNA合成的起始。