Blair G E, Dixon S C, Griffiths S A, Zajdel M E
Department of Biochemistry, University of Leeds, U.K.
Virus Res. 1989 Dec;14(4):339-46. doi: 10.1016/0168-1702(89)90026-9.
Infection of mouse BALB/c 3T3 cells by adenovirus 5 resulted in at least 1000-fold lowered yields of virus compared to human cells. The molecular basis of this restriction was analysed at the level of viral gene expression. Steady-state levels of viral DNA and RNA were greatly reduced in infected mouse, compared to human cells. Both early region 1A (E1A) and E1B mRNAs were decreased in mouse cells and their protein products were barely detectable by metabolic labelling of infected cells. The E2A-72 kDa protein and the hexon protein were detected by metabolic labelling, and immunocytochemical analysis showed that they were correctly located in nuclei of infected mouse cells. Only a minor proportion of infected mouse 3T3 cells expressed the E2A-72 kDa or hexon proteins. Low yields of virus were obtained by infection of SV40 transformed BALB/c 3T3 cells showing that SV40 does not provide a helper function for adenovirus 5 growth in this cell system.
与人类细胞相比,腺病毒5感染小鼠BALB/c 3T3细胞导致病毒产量至少降低1000倍。在病毒基因表达水平上分析了这种限制的分子基础。与人类细胞相比,感染小鼠细胞中病毒DNA和RNA的稳态水平大大降低。早期区域1A(E1A)和E1B mRNA在小鼠细胞中均减少,通过对感染细胞的代谢标记几乎检测不到它们的蛋白质产物。通过代谢标记检测到E2A-72 kDa蛋白和六邻体蛋白,免疫细胞化学分析表明它们正确定位在感染小鼠细胞的细胞核中。只有一小部分感染的小鼠3T3细胞表达E2A-72 kDa或六邻体蛋白。通过感染SV40转化的BALB/c 3T3细胞获得低产量病毒,表明SV40在该细胞系统中不为腺病毒5生长提供辅助功能。