Ertl P F, Thomas M S, Powell K L
Department of Molecular Sciences, Wellcome Research Laboratories, Beckenham, Kent, U.K.
J Gen Virol. 1991 Jul;72 ( Pt 7):1729-34. doi: 10.1099/0022-1317-72-7-1729.
The DNA polymerase genes of human cytomegalovirus (HCMV) and varicella-zoster virus (VZV) were inserted separately into the polyhedrin gene of Autographa californica nuclear polyhedrosis virus (AcNPV) by cotransfection of Spodoptera frugiperda (SF9) cells with baculovirus transfer vectors carrying the genes and AcNPV infectious DNA. Infection of SF9 cells with the recombinant viruses resulted in expression from the polyhedrin promoter of proteins of the expected Mrs. These proteins possessed DNA polymerase activities similar to that of the enzymes induced by the respective herpesvirus in infected cells, and were identified as HCMV and VZV DNA polymerase using inhibitors and specific antisera reactive with each enzyme.
通过将携带人巨细胞病毒(HCMV)和水痘 - 带状疱疹病毒(VZV)DNA聚合酶基因的杆状病毒转移载体与苜蓿银纹夜蛾核型多角体病毒(AcNPV)感染性DNA共转染草地贪夜蛾(SF9)细胞,将HCMV和VZV的DNA聚合酶基因分别插入AcNPV的多角体蛋白基因中。用重组病毒感染SF9细胞导致从多角体蛋白启动子表达预期分子量的蛋白质。这些蛋白质具有与相应疱疹病毒在感染细胞中诱导的酶相似的DNA聚合酶活性,并且使用与每种酶反应的抑制剂和特异性抗血清鉴定为HCMV和VZV DNA聚合酶。