Burnett S, Ström A C, Jareborg N, Alderborn A, Dillner J, Moreno-Lopez J, Pettersson U, Kiessling U
Department of Medical Genetics, Biomedical Center, Uppsala, Sweden.
J Virol. 1990 Nov;64(11):5529-41. doi: 10.1128/JVI.64.11.5529-5541.1990.
The bovine papillomavirus type 1 (BPV-1) genome replicates as a latent plasmid in mouse C127 cells transformed in vitro by the virus. However, we have recently shown that BPV-1 DNA amplification can be induced in a subpopulation of cells under culture conditions which suppress cell proliferation, a finding which led us to hypothesize that expression of a viral replication factor was regulated by cell growth stage. In this report, we describe the detection in these cells of abundant BPV-1 nuclear E2 antigen by immunofluorescence analysis. Expression of E2 antigen in fibropapilloma tissue was similarly localized to nonproliferating epidermal cells of the lower spinous layers--the natural site of induction of vegetative viral DNA replication. Immunoprecipitation analysis showed that the previously characterized 48-kilodalton (transactivator) and 31-kilodalton (repressor) E2 proteins were both induced in growth-arrested cell cultures. In parallel with E2 antigen synthesis under conditions of serum-deprivation in vitro, we observed a significant increase in levels of BPV-1 early region mRNAs. Furthermore, we present evidence for preferential induction of the P2443 promoter, in addition to specific induction of the P7940 promoter in response to serum deprivation. These observations indicate a central role for E2 transcription factors in the induction of viral DNA amplification in division-arrested cells in vitro and in vivo and suggest that this process is associated with a qualitative switch in the expression of viral early region genes.
牛乳头瘤病毒1型(BPV-1)基因组在经该病毒体外转化的小鼠C127细胞中作为潜伏质粒进行复制。然而,我们最近发现,在抑制细胞增殖的培养条件下,BPV-1 DNA扩增可在细胞亚群中被诱导,这一发现使我们推测病毒复制因子的表达受细胞生长阶段调控。在本报告中,我们通过免疫荧光分析描述了在这些细胞中检测到大量的BPV-1核E2抗原。纤维乳头瘤组织中E2抗原的表达同样定位于棘层下部的非增殖表皮细胞——这是营养性病毒DNA复制诱导的天然部位。免疫沉淀分析表明,先前鉴定的48千道尔顿(反式激活因子)和31千道尔顿(阻遏因子)E2蛋白在生长停滞的细胞培养物中均被诱导。与体外血清剥夺条件下E2抗原的合成同时,我们观察到BPV-1早期区域mRNA水平显著增加。此外,我们还提供了证据,证明除了P7940启动子在血清剥夺时被特异性诱导外,P2443启动子也被优先诱导。这些观察结果表明E2转录因子在体外和体内分裂停滞细胞中病毒DNA扩增的诱导中起核心作用,并表明这一过程与病毒早期区域基因表达的定性转变有关。