Ertl P F, Powell K L
Department of Molecular Sciences, Wellcome Research Laboratories, Beckenham, Kent, United Kingdom.
J Virol. 1992 Jul;66(7):4126-33. doi: 10.1128/JVI.66.7.4126-4133.1992.
Expression of the human cytomegalovirus (HCMV) (AD169) DNA polymerase gene under the control of the polyhedrin promoter of Autographa californica nuclear polyhedrosis virus in Spodoptera frugiperda (Sf9) cells has provided a source of highly active CMV DNA polymerase. In extracts from CMV-infected cells, the CMV DNA polymerase is found strongly associated with an additional polypeptide, ICP36. This protein has been identified as the CMV homolog of the herpes simplex virus type 1 UL42 gene product and may have a similar function. We have expressed HCMV DNA polymerase and ICP36 in the same system and demonstrated that they interact to form a stable complex. Moreover, ICP36 functions to stimulate the DNA polymerase activity in a template-dependent manner. We have compared the activity of the recombinant DNA polymerase in the presence and absence of ICP36 on a number of DNA templates and measured the effect of the polymerase inhibitors phosphonoformic acid and acyclovir triphosphate.
在苜蓿银纹夜蛾核型多角体病毒多角体蛋白启动子控制下,人巨细胞病毒(HCMV)(AD169)DNA聚合酶基因在草地贪夜蛾(Sf9)细胞中的表达提供了一种高活性CMV DNA聚合酶的来源。在CMV感染细胞的提取物中,发现CMV DNA聚合酶与另一种多肽ICP36紧密相关。该蛋白已被鉴定为单纯疱疹病毒1型UL42基因产物的CMV同源物,可能具有类似功能。我们已在同一系统中表达了HCMV DNA聚合酶和ICP36,并证明它们相互作用形成稳定复合物。此外,ICP36以模板依赖的方式刺激DNA聚合酶活性。我们比较了在有和没有ICP36的情况下,重组DNA聚合酶在多种DNA模板上的活性,并测定了聚合酶抑制剂膦甲酸和阿昔洛韦三磷酸的作用。