McCusker C T, Bacchetti S
Department of Pathology, McMaster University, Hamilton, Ontario, Canada.
Virus Res. 1988 Oct;11(3):199-207. doi: 10.1016/0168-1702(88)90083-4.
We have tested the responsiveness of the upstream regulatory regions (URR) of human papillomaviruses (HPV) to transactivation by the herpes simplex virus type 1 (HSV-1) immediate early proteins ICP4 (Vmw175) and ICP0 (Vmw110), using recombinant plasmids which contain URRs of HPV 1, 11 or 16 upstream of an SV40-promoted CAT gene. Transfection of the HPV-CAT plasmids into mouse cells expressing a temperature-sensitive ICP4 protein enabled us to demonstrate that ICP4 enhances transcription of the HPV 1 and 16 URRs, but not of the HPV 11 URR. Cotransfection of the HPV CAT plasmids with a plasmid encoding ICP0 indicated that only the URR of HPV 16 responded to this protein, and that the response was host cell dependent.
我们利用重组质粒测试了人乳头瘤病毒(HPV)上游调控区(URR)对单纯疱疹病毒1型(HSV-1)立即早期蛋白ICP4(Vmw175)和ICP0(Vmw110)反式激活的反应性,这些重组质粒在SV40启动子驱动的CAT基因上游含有HPV 1、11或16的URR。将HPV-CAT质粒转染到表达温度敏感型ICP4蛋白的小鼠细胞中,使我们能够证明ICP4增强了HPV 1和16 URR的转录,但没有增强HPV 11 URR的转录。HPV CAT质粒与编码ICP0的质粒共转染表明,只有HPV 16的URR对该蛋白有反应,并且这种反应是宿主细胞依赖性的。