Aboud M, Moldovan-Levin D, Salzberg S
J Virol. 1981 Feb;37(2):836-9. doi: 10.1128/JVI.37.2.836-839.1981.
Cytoplasmic viral DNA synthesis can be followed efficiently by [3H]thymidine labeling of cells exogenously infected with Moloney murine leukemia virus. Both the negative and the positive strands of viral DNA reached their maximal level in the cytoplasm at 3.5 h postinfection. Interferon treatment before infection markedly reduced the amount of viral DNA formed during the first 3.5 h, but led to a second major wave of viral DNA synthesis, peaking at 7.5 h postinfection. No such late cytoplasmic DNA synthesis occurred in the untreated control. Inhibition of protein synthesis by cycloheximide, on the other hand, stimulated cytoplasmic viral DNA synthesis during the first 3.5 h.
通过用[3H]胸苷标记外源性感染莫洛尼鼠白血病病毒的细胞,可有效地追踪细胞质中的病毒DNA合成。病毒DNA的负链和正链在感染后3.5小时在细胞质中均达到最高水平。感染前用干扰素处理显著减少了感染后最初3.5小时内形成的病毒DNA量,但导致了病毒DNA合成的第二个主要高峰,在感染后7.5小时达到峰值。未处理的对照中未发生这种晚期细胞质DNA合成。另一方面,用环己酰亚胺抑制蛋白质合成在最初3.5小时内刺激了细胞质中的病毒DNA合成。