Goorha R
J Virol. 1982 Aug;43(2):519-28. doi: 10.1128/JVI.43.2.519-528.1982.
Viral DNA synthesis in frog virus 3 (FV3)-infected cells occurs both in the nucleus and in the cytoplasm (Goorha et al., Virology 84:32-51, 1978). Relationships between viral DNA molecules synthesized in these two compartments and their role in the virus replication were examined. The data presented here suggest that (i) FV3 DNA replicated in two stages and (ii) nucleus and cytoplasm were the sites of stages 1 and 2 of DNA replication, respectively. Stages 1 and 2 were further distinguished by their temporal appearance during infection and by the sizes of the replicating DNA as determined by sedimentation in neutral sucrose gradients. In stage 1, replicating molecules, between the size of unit and twice the unit length, were produced early in infection (2 h postinfection). In contrast, stage 2 of DNA replication occurred only after 3 h postinfection, and replicating molecules were large concatemers. Results of pulse-chase experiments showed that the concatemeric DNA served as the precursor for the production of mature FV3 DNA. Denaturation of concatemeric DNA with alkali or digestion with S1 nuclease reduced it to less than genome size molecules, indicating the presence of extensive single-stranded regions. Analysis of replicating DNA by equilibrium centrifugation in CsCl gradients after a pulse-chase suggested that these single-stranded regions were subsequently repaired. Based on these and previous data, a scheme of FV3 replication is presented. According to this scheme, FV3 utilizes the nucleus for early transcription and stage 1 of DNA replication. The viral DNA is then transported to the cytoplasm, where it participates in stage 2 DNA replication to form a concatemeric replication complex. The processing of concatemers to produce mature viral DNA and virus assembly also occurs in the cytoplasm. This mode of replication is strikingly different from any other known DNA virus.
蛙病毒3(FV3)感染细胞中的病毒DNA合成发生在细胞核和细胞质中(戈尔哈等人,《病毒学》84:32 - 51,1978)。研究了在这两个区室中合成的病毒DNA分子之间的关系及其在病毒复制中的作用。此处呈现的数据表明:(i)FV3 DNA分两个阶段复制;(ii)细胞核和细胞质分别是DNA复制第1阶段和第2阶段的发生位点。第1阶段和第2阶段在感染期间的出现时间以及通过中性蔗糖梯度沉降测定的复制DNA大小方面进一步区分。在第1阶段,感染早期(感染后2小时)产生大小在单位长度和单位长度两倍之间的复制分子。相比之下,DNA复制的第2阶段仅在感染后3小时才发生,并且复制分子是大的多联体。脉冲追踪实验结果表明,多联体DNA是产生成熟FV3 DNA的前体。用碱使多联体DNA变性或用S1核酸酶消化会使其减少到小于基因组大小的分子,表明存在广泛的单链区域。脉冲追踪后通过在CsCl梯度中进行平衡离心分析复制DNA表明,这些单链区域随后被修复。基于这些以及先前的数据,提出了FV3复制的方案。根据该方案,FV3利用细胞核进行早期转录和DNA复制的第1阶段。然后病毒DNA被转运到细胞质中,在那里它参与第2阶段的DNA复制以形成多联体复制复合体。多联体加工以产生成熟病毒DNA和病毒组装也发生在细胞质中。这种复制模式与任何其他已知的DNA病毒显著不同。