Feigenbaum L, Khalili K, Major E, Khoury G
Proc Natl Acad Sci U S A. 1987 Jun;84(11):3695-8. doi: 10.1073/pnas.84.11.3695.
Human papovavirus JCV is associated with the human demyelinating disorder progressive multifocal leukoencephalopathy. In tissue culture, the virus is largely restricted to growth in primary human fetal glial cell. In this study, we demonstrate two levels of regulation of the viral host range. Expression of the early JCV mRNA, which encodes the essential viral protein, large tumor antigen (T antigen), depends on recognition of the early enhancer/promoter elements by tissue-specific factors found in both human and rodent glial cells. In the presence of JCV T antigen, viral DNA replication requires a species-specific factor, presumably a component of DNA polymerase, which is found in a wide range of primate cells. We further demonstrate that simian virus 40 T antigen has sufficient homology to efficiently substitute for the analogous JCV protein in initiating viral DNA replication.
人乳头多瘤空泡病毒JCV与人类脱髓鞘疾病进行性多灶性白质脑病相关。在组织培养中,该病毒主要局限于在原代人胎儿神经胶质细胞中生长。在本研究中,我们证明了病毒宿主范围的两个调控水平。早期JCV mRNA的表达,其编码必需的病毒蛋白大肿瘤抗原(T抗原),取决于人类和啮齿动物神经胶质细胞中发现的组织特异性因子对早期增强子/启动子元件的识别。在JCV T抗原存在的情况下,病毒DNA复制需要一种物种特异性因子,推测是DNA聚合酶的一个组分,它存在于多种灵长类细胞中。我们进一步证明,猿猴病毒40 T抗原具有足够的同源性,能够在启动病毒DNA复制时有效地替代类似的JCV蛋白。