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首页> 外文期刊>Journal of Virology >Measles Virus Ribonucleic Acid and Protein Synthesis: Effects of 6-Azauridine and Cycloheximide on Viral Replication
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Measles Virus Ribonucleic Acid and Protein Synthesis: Effects of 6-Azauridine and Cycloheximide on Viral Replication

机译:麻疹病毒核糖核糖酸和蛋白质合成:6-氮酮和环己酰亚胺对病毒复制的影响

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摘要

Cycloheximide and 6-azauridine were employed to study the time course of measles virus protein and nucleic acid syntheses in AV3 cells. Synthesis of ribonucleic acid (RNA) essential for infectivity was first detected at 6 hr and increased concurrently with the formation of essential protein. Maximum levels of virus-specific RNA and protein were present by 18 hr, a time when only 5% of progeny virus was detected. Essential RNA and protein syntheses preceded the formation of infectious virus by at least 10 to 12 hr. The time course of RNA and protein syntheses essential for the formation of complement-fixing (CF) antigen and salt-dependent agglutinin (SDA) was also determined. RNA synthesis essential for the formation of SDA was first detected at 2 hr and was present maximally by 6 hr, whereas SDA-protein increased concurrently with the protein essential for infectivity. This suggested that the last protein essential for infectivity may be SDA. RNA synthesis essential for the formation of CF antigen was first detected at 4 hr, while CF-protein increased at 5 hr and preceded SDA-protein and protein essential for infectivity by approximately 3 hr. Reversal of inhibition of protein synthesis by cycloheximide indicated that early protein synthesis (1 to 3 hr) was required for the formation of infectious virus. The data suggest that the relatively long eclipse period observed with measles virus is related to a long maturation period rather than to late formation of early proteins, viral RNA, or structural proteins.
机译:使用环己酰亚胺和6-氮酮在AV3细胞中研究麻疹病毒蛋白和核酸合成的时间过程。首先在6小时内检测到感染性必需的核糖核酸(RNA),并随着必需蛋白质的形成同时增加。最大程度的病毒特异性RNA和蛋白质是18小时的,当检测到仅5%的后代病毒时的时间是时间。基本RNA和蛋白质合成在形成传染性病毒的形成至少10至12小时。还测定了对形成补体固定(CF)抗原和盐依赖性凝集素(SDA)的形成的RNA和蛋白质合成的时间过程。首先在2小时以2小时检测到形成SDA的RNA合成,并最大限度地以6小时最大化,而SDA-蛋白同时随着感染性必需的蛋白质而增加。这表明对感染性至关重要的最后蛋白质可能是SDA。首先在4小时以4小时检测到形成CF抗原的RNA合成,而CF-蛋白在5小时和前面的SDA-蛋白质和蛋白质中升高约3小时。环己酰亚胺的蛋白质合成抑制的反转表明,形成传染性病毒所需的早期蛋白质合成(1至3小时)。该数据表明,用麻疹病毒观察到的相对长的Eclipse周期与较长的成熟时期,而不是晚期形成早期蛋白质,病毒RNA或结构蛋白。

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