Institute of Virology, Saarland University, Kirrbergerstrasse, Building 47, 66421 Homburg/Saar, Germany.
J Virol. 2010 Feb;84(3):1376-86. doi: 10.1128/JVI.01220-09. Epub 2009 Nov 18.
The papillomavirus life cycle parallels keratinocyte differentiation in stratifying epithelia. We have previously shown that the human papillomavirus type 8 (HPV8) E2 protein downregulates beta4-integrin expression in normal human keratinocytes, which may trigger subsequent differentiation steps. Here, we demonstrate that the DNA binding domain of HPV8 E2 is sufficient to displace a cellular factor from the beta4-integrin promoter. We identified the E2-displaceable factor as activator protein 1 (AP-1), a heteromeric transcription factor with differentiation-specific expression in the epithelium. beta4-Integrin-positive epithelial cells displayed strong AP-1 binding activity. Both AP-1 binding activity and beta4-integrin expression were coregulated during keratinocyte differentiation suggesting the involvement of AP-1 in beta4-integrin expression. In normal human keratinocytes the AP-1 complex was composed of JunB and Fra-1 subunits. Chromatin immunoprecipitation assays confirmed that JunB/Fra-1 proteins interact in vivo with the beta4-integrin promoter and that JunB/Fra-1 promoter occupancy is reduced during keratinocyte differentiation as well as in HPV8 E2 positive keratinocytes. Ectopic expression of the tethered JunB/Fra-1 heterodimer in normal human keratinocytes activated the beta4-integrin promoter, while coexpression of HPV8 E2 reverted the JunB/Fra-1 effect. In summary, we identified a novel mechanism of human beta4-integrin regulation that is specifically targeted by the HPV8 E2 protein mimicking transcriptional conditions of differentiation. This may explain the early steps of how HPV8 commits its host cells to the differentiation process required for the viral life cycle.
乳头瘤病毒生命周期与分层上皮角质细胞分化平行。我们之前已经表明,人乳头瘤病毒 8 型(HPV8)E2 蛋白下调正常人类角质细胞中β4-整联蛋白的表达,这可能触发随后的分化步骤。在这里,我们证明 HPV8 E2 的 DNA 结合域足以将细胞因子从β4-整联蛋白启动子上置换下来。我们鉴定出 E2 可置换因子为激活蛋白 1(AP-1),这是一种在表皮中有分化特异性表达的异源二聚体转录因子。β4-整联蛋白阳性上皮细胞显示出强烈的 AP-1 结合活性。在角质细胞分化过程中,β4-整联蛋白表达和 AP-1 结合活性均受到共同调控,提示 AP-1 参与了β4-整联蛋白的表达。在正常的人类角质细胞中,AP-1 复合物由 JunB 和 Fra-1 亚基组成。染色质免疫沉淀实验证实了 JunB/Fra-1 蛋白在体内与β4-整联蛋白启动子相互作用,并且 JunB/Fra-1 启动子占据在角质细胞分化过程中以及 HPV8 E2 阳性角质细胞中减少。在正常的人类角质细胞中异位表达束缚的 JunB/Fra-1 异二聚体激活了β4-整联蛋白启动子,而共表达 HPV8 E2 则逆转了 JunB/Fra-1 的作用。总之,我们鉴定出一种新的人类β4-整联蛋白调控机制,该机制被 HPV8 E2 蛋白特异性靶向,模拟了分化的转录条件。这可能解释了 HPV8 将宿主细胞定向到病毒生命周期所需的分化过程的早期步骤。