Quinlan M P, Knipe D M
Mol Cell Biol. 1985 May;5(5):957-63. doi: 10.1128/mcb.5.5.957-963.1985.
We examined the expression and localization of herpesvirus proteins in monkey cells transfected with recombinant plasmids containing herpes simplex virus (HSV) DNA sequences. Low levels of expression of the major HSV DNA-binding protein ICP8 were observed when ICP8-encoding plasmids were introduced into cells alone. ICP8 expression was greatly increased when a recombinant plasmid encoding the HSV alpha (immediate-early) ICP4 and ICP0 genes was transfected with the ICP8 gene. Deletion and subcloning analysis indicated that two separate functions capable of stimulating ICP8 expression were encoded on the alpha gene plasmid. One mapped in or near the ICP4 gene, and one mapped in or near the ICP0 gene. Their stimulatory effects were synergistic when introduced on two separate plasmids. Thus, two separate viral functions can activate herpesvirus early gene expression in transfected cells.
我们检测了用含有单纯疱疹病毒(HSV)DNA序列的重组质粒转染的猴细胞中疱疹病毒蛋白的表达和定位。当单独将编码ICP8的质粒导入细胞时,观察到主要的HSV DNA结合蛋白ICP8表达水平较低。当编码HSVα(立即早期)ICP4和ICP0基因的重组质粒与ICP8基因一起转染时,ICP8的表达大大增加。缺失和亚克隆分析表明,α基因质粒上编码了两种能够刺激ICP8表达的独立功能。一种定位在ICP4基因内或附近,另一种定位在ICP0基因内或附近。当它们分别导入两个单独的质粒时,其刺激作用具有协同性。因此,两种独立的病毒功能可以激活转染细胞中的疱疹病毒早期基因表达。