Detjen B M, Walden W E, Thach R E
J Biol Chem. 1982 Aug 25;257(16):9855-60.
The specificity of protein synthesis in reovirus-infected mouse SC-1 cells was investigated, with the following results: a, extracts from infected and control cells translated saturating levels of capped globin mRNA with the same efficiency; b, infected cell extracts did not display a virus-induced increase in the capacity to translate decapped globin mRNA; c, translation of both cellular and viral messages was equally sensitive to the cap analog, 7-methylguanosine 5'-triphosphate. These findings are consistent with a previously published model (Walden, W., Godefroy-Colburn, T., and Thach, R. E. (1981) J. Biol. Chem. 256, 11739-11746) in which translation rates in reovirus-infected SC-1 cells are regulated by competition of capped host and viral mRNAs for a component of the unaltered protein synthetic system. Similar experimental results were obtained using reovirus-infected mouse L cells, with the following exceptions: a, the shutoff of host translation was far greater in L cells than in SC-1 cells; b, extracts of infected L cells were less active than controls for translation of all mRNAs tested. The reasons for the differences between SC-1 cells and L cells in their response to reovirus infection are being investigated.
对呼肠孤病毒感染的小鼠SC-1细胞中蛋白质合成的特异性进行了研究,结果如下:a,感染细胞和对照细胞的提取物以相同效率翻译饱和水平的加帽珠蛋白mRNA;b,感染细胞提取物在翻译去帽珠蛋白mRNA的能力上未表现出病毒诱导的增加;c,细胞和病毒信息的翻译对帽类似物7-甲基鸟苷5'-三磷酸同样敏感。这些发现与先前发表的模型(Walden, W., Godefroy-Colburn, T., and Thach, R. E. (1981) J. Biol. Chem. 256, 11739 - 11746)一致,在该模型中,呼肠孤病毒感染的SC-1细胞中的翻译速率由加帽的宿主和病毒mRNA竞争未改变的蛋白质合成系统的一个组分来调节。使用呼肠孤病毒感染的小鼠L细胞获得了类似的实验结果,但有以下例外:a,L细胞中宿主翻译的关闭比SC-1细胞中要大得多;b,感染的L细胞提取物对所有测试mRNA的翻译活性低于对照。正在研究SC-1细胞和L细胞对呼肠孤病毒感染反应不同的原因。