Laux G, Freese U K, Fischer R, Polack A, Kofler E, Bornkamm G W
Institut fur Virologie, Zentrum fur Hygiene, Albert-Ludwigs-Universitet Freiburg, Federal Republic of Germany.
Virology. 1988 Feb;162(2):503-7. doi: 10.1016/0042-6822(88)90496-5.
A number of agents including the tumor promoter 12-O-tetradecanoylphorbol-13-acetate (TPA) can induce an abortive virus cycle in the EBV nonproducer Burkitt's lymphoma line Raji. We describe the pattern of viral RNAs transcribed in uninduced cells and in cells treated with TPA for 8 hr, as analyzed by Northern blotting. By comparing the patterns of RNAs observed in cells treated with TPA, TPA plus cycloheximide, or cycloheximide alone, we have tested whether any EBV gene in TPA-treated Raji cells would be inducible directly by TPA in the presence of protein synthesis inhibitors, similarly to immediate-early genes induced by superinfection of Raji cells with P3HR-1 virus in the presence of cycloheximide. We demonstrate here that induction of all early EBV genes is dependent on ongoing protein synthesis. The experiments do not provide an answer to whether TPA acts by activating an initial step in the cascade of virus production or whether TPA has a simultaneous pleiotropic effect on the regulation of a large number of viral genes.
包括肿瘤启动子12 - O - 十四烷酰佛波醇 - 13 - 乙酸酯(TPA)在内的多种因子可在EBV非生产性伯基特淋巴瘤细胞系Raji中诱导一个流产性病毒周期。我们描述了在未诱导细胞以及用TPA处理8小时的细胞中转录的病毒RNA模式,通过Northern印迹法进行分析。通过比较在用TPA、TPA加放线菌酮或单独用放线菌酮处理的细胞中观察到的RNA模式,我们测试了在蛋白质合成抑制剂存在的情况下,TPA处理的Raji细胞中的任何EBV基因是否会被TPA直接诱导,类似于在放线菌酮存在的情况下用P3HR - 1病毒超感染Raji细胞所诱导的立即早期基因。我们在此证明,所有EBV早期基因的诱导都依赖于正在进行的蛋白质合成。这些实验并未回答TPA是通过激活病毒产生级联反应中的初始步骤起作用,还是TPA对大量病毒基因的调控具有同时的多效性作用。