Bauknecht T, See R H, Shi Y
Department of Pathology, Harvard Medical School, Boston, Massachusetts 02115, USA.
J Virol. 1996 Nov;70(11):7695-705. doi: 10.1128/JVI.70.11.7695-7705.1996.
The human papillomavirus type 18 (HPV-18) upstream regulatory region (URR) controls viral gene transcription in a cell-type-specific manner. The HPV-18 URR is active in HeLa cells but inactive in HepG2 cells. The activating activity of YY1 in HeLa cells is dependent on its functional interactions with the switch region which is critical for the HPV-18 URR activity in HeLa cells. Here, we show that a protein complex composed of C/EBP beta and YY1 binds the switch region which is detected only in HeLa cells, not in HepG2 cells. Transfection of C/EBP beta into HepG2 cells restored the formation of the C/EBP beta-YY1-switch region complex, accompanied by increased transcription directed by the HPV-18 URR. Mutations in the switch region that abolished the complex formation also abrogated C/EBP beta-induced transcriptional activation. This provides a strong correlation between the binding of the C/EBP beta-YY1 complex to the switch region and cell-type-specific URR activity. Taken together, we have identified a novel C/EBP beta-YY1 complex that binds the switch region and contributes to cell-type-specific HPV-18 URR activity.
人乳头瘤病毒18型(HPV - 18)上游调控区(URR)以细胞类型特异性方式控制病毒基因转录。HPV - 18 URR在HeLa细胞中具有活性,但在HepG2细胞中无活性。YY1在HeLa细胞中的激活活性取决于其与开关区域的功能相互作用,而开关区域对于HPV - 18 URR在HeLa细胞中的活性至关重要。在此,我们表明由C/EBPβ和YY1组成的蛋白质复合物结合开关区域,该区域仅在HeLa细胞中检测到,而在HepG2细胞中未检测到。将C/EBPβ转染到HepG2细胞中可恢复C/EBPβ - YY1 - 开关区域复合物的形成,并伴随着HPV - 18 URR指导的转录增加。开关区域中消除复合物形成的突变也消除了C/EBPβ诱导的转录激活。这在C/EBPβ - YY1复合物与开关区域的结合和细胞类型特异性URR活性之间建立了强烈的相关性。综上所述,我们鉴定出一种新型的C/EBPβ - YY1复合物,其结合开关区域并有助于细胞类型特异性HPV - 18 URR活性。