Chu P W, Westaway E G
Virology. 1985 Jan 15;140(1):68-79. doi: 10.1016/0042-6822(85)90446-5.
Only three forms of Kunjin virus-specified RNA were isolated from cytoplasm early after the latent period (about 15 hr) viz., 44 S genomic-sized single-stranded RNA, 20 S double-stranded "replicative form" (RF), and 20-28 S partially ribonuclease-resistant (about 70%) "replicative intermediate" (RI). The RF and RI were resolved by electrophoresis in aqueous-agarose gel only following LiCl fractionation. The RI did not enter urea-polyacrylamide gels. After denaturation of untreated or RNase-treated RI and RF, only 44 S RNA was present in electropherograms. RNA polymerase activity at 8 hr postinfection was detected by in vitro assays of cytoplasmic extracts and reached a maximum at 24 hr, the only major labeled product being RF; a trace amount of free 44 S RNA was also produced. These results, and the kinetics of incorporation of [3H]uridine into RI, RF, and 44 S RNA in pulse and pulse-chase experiments, formed the basis of a model in which flavivirus RF functions as a recycling template for semiconservative and (mainly) asymmetric replication, on which only one nascent strand is synthesized per cycle.
在潜伏期(约15小时)后早期,仅从细胞质中分离出三种昆金病毒特异性RNA,即44S基因组大小的单链RNA、20S双链“复制型”(RF)和20 - 28S部分抗核糖核酸酶(约70%)的“复制中间体”(RI)。仅在LiCl分级分离后,RF和RI才能通过在水琼脂糖凝胶中的电泳分离。RI不能进入尿素 - 聚丙烯酰胺凝胶。在未处理或经核糖核酸酶处理的RI和RF变性后,电泳图谱中仅存在44S RNA。通过对细胞质提取物的体外测定,在感染后8小时检测到RNA聚合酶活性,并在24小时达到最大值,唯一的主要标记产物是RF;还产生了微量的游离44S RNA。这些结果以及在脉冲和脉冲追踪实验中[3H]尿苷掺入RI、RF和44S RNA的动力学,构成了一个模型的基础,在该模型中,黄病毒RF作为半保留和(主要)不对称复制的循环模板,每个循环仅合成一条新生链。