Wu Jun, O'Neill Joseph, Barbosa Miguel S
Signal Research Division of Celgene, 5555 Oberlin Drive, San Diego, CA 92121, USA1.
J Gen Virol. 2001 May;82(Pt 5):1147-1155. doi: 10.1099/0022-1317-82-5-1147.
Toward understanding the temporal regulation of human cytomegalovirus (HCMV) late genes, we studied the regulation of the late gene promoter (pp28US, UL99) when outside the context of the viral genome and its response to the immediate early (IE) proteins. Expression of the luciferase reporter gene, regulated by the pp28US promoter, was synchronous with that of the endogenous viral pp28 gene, independently of whether the reporter was episomal or integrated into the glioblastoma cell line U373MG. Cotransfection of the reporter with expression vectors for each of the three major IE genes, IE72, IE86 and IE55, indicated that only IE86 transactivated the pp28US promoter. However, the magnitude of the promoter activation upon HCMV infection suggested that additional factors are also required for higher promoter activity. The promoter activation was specific to HCMV, as herpes simplex virus type 1 infection did not induce luciferase expression.
为了理解人类巨细胞病毒(HCMV)晚期基因的时间调控,我们研究了病毒基因组外晚期基因启动子(pp28US,UL99)的调控及其对立即早期(IE)蛋白的反应。由pp28US启动子调控的荧光素酶报告基因的表达与内源性病毒pp28基因的表达同步,无论报告基因是游离的还是整合到胶质母细胞瘤细胞系U373MG中。将报告基因与三个主要IE基因IE72、IE86和IE55的表达载体共转染,结果表明只有IE86能反式激活pp28US启动子。然而,HCMV感染后启动子激活的程度表明,更高的启动子活性还需要其他因素。启动子激活是HCMV特有的,因为1型单纯疱疹病毒感染不会诱导荧光素酶表达。