Yamaura I, Cavalieri L F
J Virol. 1978 Aug;27(2):300-6. doi: 10.1128/JVI.27.2.300-306.1978.
We studied the kinetics of the reverse transcription of 70S and 35S RNA of avian myeloblastosis virus in the presence and absence of various tRNA's. All tRNA's inhibited synthesis. tRNA's from Escherichia coli and yeast exhibited a noncompetitive type of inhibition, i.e., they bound reversibly and randomly and did not alter the affinity of the viral RNA for the polymerase. Nonprimer tRNA's obtained from 70S RNA molecules produced a complex pattern of inhibition. The results show that the nonprimer tRNA's which bound to the reverse transcriptase decreased the affinity of the viral RNA for the enzyme. The maximum rate of synthesis with 70S RNA as the template was less than that with 35S RNA, presumably because the former contains nonprimer tRNA's which can interact with the polymerase.
我们研究了在有和没有各种转运RNA(tRNA)存在的情况下,禽成髓细胞瘤病毒70S和35S RNA逆转录的动力学。所有tRNA均抑制合成。来自大肠杆菌和酵母的tRNA表现出非竞争性抑制类型,即它们可逆且随机结合,并且不会改变病毒RNA对聚合酶的亲和力。从70S RNA分子获得的非引物tRNA产生了复杂的抑制模式。结果表明,与逆转录酶结合的非引物tRNA降低了病毒RNA对该酶的亲和力。以70S RNA为模板的最大合成速率低于以35S RNA为模板的最大合成速率,推测是因为前者含有可与聚合酶相互作用的非引物tRNA。