Zaĭdes V M, Farashian V R, Boshchenko Iu A, Zhdanov V M
Biokhimiia. 1981 Dec;46(12):2174-8.
The monolayer cultures of chicken embryonic cells were infected with influenza virus and 6 hrs after the infection the relative concentrations of viral mRNAs and the relative rates of virus-specific protein synthesis were determined. For this purpose the infected cells were incubated under conditions of continuous labelling of RNAs by the radioactive precursor; the mRNA fraction was obtained by hybridization of total RNA of infected cells with non-labelled RNA of viral particles and the individual mRNAs were fractionated by polyacrylamide gel electrophoresis of RNA duplexes. The proteins from infected cells were labelled by [14C] amino acids for a short time and the individual virus-specific proteins were separated electrophoretically. There was no correlation between the rates of virus-specific protein synthesis and the relative concentrations of corresponding mRNAs. This indicates the regulation of virus-specific protein synthesis at the post-translational level.
用流感病毒感染鸡胚细胞单层培养物,感染后6小时测定病毒mRNA的相对浓度和病毒特异性蛋白质合成的相对速率。为此,将感染的细胞在放射性前体连续标记RNA的条件下孵育;通过将感染细胞的总RNA与病毒颗粒的未标记RNA杂交获得mRNA部分,并通过RNA双链体的聚丙烯酰胺凝胶电泳对各个mRNA进行分级分离。用[14C]氨基酸对感染细胞的蛋白质进行短时间标记,并通过电泳分离各个病毒特异性蛋白质。病毒特异性蛋白质合成速率与相应mRNA的相对浓度之间没有相关性。这表明在翻译后水平上对病毒特异性蛋白质合成进行调控。