Su H K, Courtney R J
Department of Biochemistry and Molecular Biology, Louisiana State University Medical Center, Shreveport 71130-3932.
J Virol. 1988 Oct;62(10):3668-74. doi: 10.1128/JVI.62.10.3668-3674.1988.
The gG-2 glycoprotein gene of herpes simplex virus type 2 (HSV-2) was cloned into the mammalian expression vector pMSG under the control of the inducible mouse mammary tumor virus promoter. Transfection of this cloned gG-2 construct into NIH 3T3 cells resulted in the stable expression of gG-2 upon induction with dexamethasone. In addition, the 104,000-molecular-weight (104K) and 72K gG-2 precursors as well as the 34K secreted component were generated in the transformed cells. The synthesis of gG-2 in these transformed cells appeared to follow the same cleavage-processing pathway as gG-2 synthesis during an HSV-2 infection. These results indicate that the processing of gG-2 can occur in the absence of an HSV-2 infection.
将2型单纯疱疹病毒(HSV - 2)的gG - 2糖蛋白基因克隆到受诱导型小鼠乳腺肿瘤病毒启动子控制的哺乳动物表达载体pMSG中。将此克隆的gG - 2构建体转染到NIH 3T3细胞中,用地塞米松诱导后可导致gG - 2的稳定表达。此外,在转化细胞中产生了分子量为104,000(104K)和72K的gG - 2前体以及34K的分泌成分。这些转化细胞中gG - 2的合成似乎遵循与HSV - 2感染期间gG - 2合成相同的切割加工途径。这些结果表明,gG - 2的加工可以在没有HSV - 2感染的情况下发生。