Wymer J P, Aurelian L
Department of Pharmacology and Experimental Therapeutics, University of Maryland School of Medicine, Baltimore 21201.
J Gen Virol. 1990 Aug;71 ( Pt 8):1817-21. doi: 10.1099/0022-1317-71-8-1817.
Activation of the herpes simplex virus type 2 (HSV-2) large subunit of the ribonucleotide reductase (ICP10) gene by papillomavirus DNA encoding the E2 or E7 proteins was studied directly by immunofluorescence or by chloramphenicol acetyltransferase (CAT) analysis with hybrid ICP10 or IE175 and 38K promoter constructions. Cotransfection with bovine papillomavirus type 1 or human papillomavirus type 16 (HPV-16) E2 DNA enhanced CAT expression from constructions in which CAT is regulated by the ICP10 but not by other HSV promoters. Expression was not enhanced by cotransfection with HPV-16 E7 DNA. Sequence analysis of the ICP10 promoter identified a consensus E2-binding motif. Activation was significantly reduced by site-directed mutagenesis of the consensus motif.
通过免疫荧光法,或使用杂交的ICP10或IE175及38K启动子构建体进行氯霉素乙酰转移酶(CAT)分析,直接研究了编码E2或E7蛋白的乳头瘤病毒DNA对单纯疱疹病毒2型(HSV-2)核糖核苷酸还原酶大亚基(ICP10)基因的激活作用。用1型牛乳头瘤病毒或16型人乳头瘤病毒(HPV-16)E2 DNA共转染,可增强由ICP10而非其他HSV启动子调控CAT的构建体中的CAT表达。与HPV-16 E7 DNA共转染不会增强表达。对ICP10启动子的序列分析确定了一个共有E2结合基序。通过对该共有基序进行定点诱变,激活作用显著降低。