Pari G S, St Jeor S C
Department of Microbiology, University of Nevada, Reno 89507.
Virology. 1990 Dec;179(2):785-94. doi: 10.1016/0042-6822(90)90146-i.
Previously we had reported that human cytomegalovirus (HCMV) induced replication of plasmids containing the SV40 origin of replication in human fibroblasts that were nonpermissive for SV40 and permissive for HCMV DNA replication. The amplification of SV40 origin-containing plasmids was dependent upon the HCMV-induced expression of T-antigen RNA. From previous studies it was determined that cotransfection of cosmids, containing HCMV genomic DNA, could stimulate SV40 DNA replication and T-antigen production. This indicated that the gene products of HCMV responsible for inducing SV40 DNA replication could be determined. In this study we report that the cotransfection of the major IE gene of HCMV alone was sufficient to facilitate the replication of the SV40 origin-containing plasmid. The HCMV IE1 gene product (i) increased expression of T-antigen RNA and protein and (ii) induced SV40 plasmid DNA replication in a T-antigen-dependent manner. The SV40 replication event was not due only to the expression of T-antigen. When the gene coding for T-antigen was placed under control of the Rous sarcoma viral promoter so that T-antigen expression in HEL cells was constitutive, it was not sufficient to replicate the SV40 plasmid in the absence of the HCMV IE1 protein. Therefore, the major IE gene of HCMV was capable of increasing the expression of T-antigen RNA and facilitating the replication of the SV40 origin. We are currently investigating the mechanism responsible for these observations.
此前我们曾报道,人巨细胞病毒(HCMV)可诱导含SV40复制起点的质粒在对SV40不敏感但对HCMV DNA复制敏感的人成纤维细胞中复制。含SV40起点质粒的扩增依赖于HCMV诱导的T抗原RNA表达。根据以往研究确定,共转染含HCMV基因组DNA的黏粒可刺激SV40 DNA复制和T抗原产生。这表明负责诱导SV40 DNA复制的HCMV基因产物是可以确定的。在本研究中,我们报道单独共转染HCMV的主要立即早期(IE)基因就足以促进含SV40起点质粒的复制。HCMV IE1基因产物(i)增加了T抗原RNA和蛋白质的表达,并且(ii)以T抗原依赖的方式诱导了SV40质粒DNA复制。SV40复制事件并非仅由T抗原的表达所致。当将编码T抗原的基因置于劳氏肉瘤病毒启动子的控制之下,使得HEL细胞中T抗原的表达是组成型的时,在没有HCMV IE1蛋白的情况下,这不足以使SV40质粒复制。因此,HCMV的主要IE基因能够增加T抗原RNA的表达并促进SV40起点的复制。我们目前正在研究导致这些观察结果的机制。