Martinet C, Combard A, Printz-Ané C, Printz P
J Virol. 1979 Jan;29(1):123-33. doi: 10.1128/JVI.29.1.123-133.1979.
Temperature-sensitive (ts) mutants of vesicular stomatitis virus belonging to complementation groups III and V were investigated for their in vivo RNA synthesis. The sucrose gradient patterns of the RNA species which they produced at nonpermissive temperature (39.2 degrees C) were systematically compared under different experimental conditions: variation of input multiplicity and of time of infection, superinfection with T particles, and temperature shifts. Finally, a more precise analysis of the various RNA species synthesized was carried out. It appeared that the characteristics of RNA synthesis specified at 39.2 degrees C by tsIII or tsV mutants differed from the normal RNA synthesis of vesicular stomatitis virus wild type. Their common depression at 39.2 degrees C in virion-like RNA (38S) production--i.e., so-called genome replication--was tentatively paralleled with the concomitant ts events which have been previously shown to affect the two viral envelope proteins. An overproduction of the RNA transcripts was described for mutants in group III and posed the question of a regulation process to determine the amount of RNA to be transcribed.
对属于互补群III和V的水泡性口炎病毒温度敏感(ts)突变体进行了体内RNA合成研究。在不同实验条件下,系统比较了它们在非允许温度(39.2℃)下产生的RNA种类的蔗糖梯度图谱:输入复数和感染时间的变化、T颗粒的超感染以及温度转换。最后,对合成的各种RNA种类进行了更精确的分析。结果表明,tsIII或tsV突变体在39.2℃下指定的RNA合成特征与水泡性口炎病毒野生型的正常RNA合成不同。它们在39.2℃下病毒样RNA(38S)产生(即所谓的基因组复制)方面的共同降低,初步与先前已证明影响两种病毒包膜蛋白的伴随ts事件相平行。III组突变体的RNA转录本过量产生,这提出了一个调节过程的问题,以确定要转录的RNA量。