Department of Biology, Indiana University, Simon Hall, 212 South Hawthorne Drive, Bloomington, IN 47405-7003, USA.
Virology. 2013 Jul 5;441(2):171-81. doi: 10.1016/j.virol.2013.03.022. Epub 2013 Apr 17.
Sindbis virus subgenomic mRNA is efficiently translated in infected vertebrate cells whereas host translation is shut-off. Deletions in the 5'UTR of the subgenomic mRNA were made to investigate its role in viral gene expression. Deletion of nucleotides 1-10 and 11-20 caused a small plaque phenotype, reduced levels of subgenomic mRNA and structural proteins, and increased expression of nonstructural proteins. Whereas deletion 1-10 virus inhibited cellular protein synthesis, deletion 11-20 did so inefficiently. A large plaque revertant of deletion 11-20, possessing a duplication of the subgenomic promoter region, produced subgenomic mRNA at WT levels and restored inhibition of host protein synthesis. Further analysis of the mutant and revertant 5'UTR sequences showed the ability to shut-off host cell translation correlated with the efficiency of translation of subgenomic mRNA. We propose that the translational efficiency and quantity of the subgenomic mRNA play a role in inhibition of host cell translation.
辛德毕斯病毒亚基因组 mRNA 在受感染的脊椎动物细胞中能高效翻译,而宿主翻译则被关闭。为了研究亚基因组 mRNA 在病毒基因表达中的作用,我们对其 5'UTR 进行了缺失。亚基因组 mRNA 的 1-10 核苷酸和 11-20 核苷酸缺失导致小斑表型、亚基因组 mRNA 和结构蛋白水平降低,以及非结构蛋白表达增加。而缺失 1-10 病毒抑制细胞蛋白合成,缺失 11-20 病毒则效率低下。缺失 11-20 的大斑回复突变体,具有亚基因组启动子区域的重复,产生了与 WT 水平相当的亚基因组 mRNA,并恢复了对宿主蛋白合成的抑制。对突变体和回复突变体 5'UTR 序列的进一步分析表明,关闭宿主细胞翻译的能力与亚基因组 mRNA 翻译的效率相关。我们提出,亚基因组 mRNA 的翻译效率和数量在抑制宿主细胞翻译中起作用。