Sze P, Herman R C
Syntex Research, Palo Alto, CA 94304.
Virus Res. 1992 Nov;26(2):141-52. doi: 10.1016/0168-1702(92)90153-z.
Expression from the promoter for the large subunit (ICP6) of the ribonucleotide reductase encoded by herpes simplex virus type 1 (HSV-1) has been examined. Using the lacZ reporter gene fused in-frame with ICP6 regulatory sequences to assay expression quantitatively, we showed that the ICP6 promoter responded very weakly to the alpha-transinducing factor (TIF) in the absence of all other viral gene products, but much more strongly to immediate early proteins. Similar patterns of regulation were observed when the reporter gene construct was located at two different positions within the the viral genome or in a stably transfected Vero cell line. Infection of the stably transfected cells with various HSV-1 mutants identified ICP0 as the major transactivator of the ICP6 promoter.
对单纯疱疹病毒1型(HSV-1)编码的核糖核苷酸还原酶大亚基(ICP6)启动子的表达进行了研究。使用与ICP6调控序列框内融合的lacZ报告基因来定量分析表达,我们发现,在没有所有其他病毒基因产物的情况下,ICP6启动子对α反式诱导因子(TIF)的反应非常微弱,但对立即早期蛋白的反应要强得多。当报告基因构建体位于病毒基因组内的两个不同位置或稳定转染的Vero细胞系中时,观察到了类似的调控模式。用各种HSV-1突变体感染稳定转染的细胞,确定ICP0是ICP6启动子的主要反式激活因子。