Toots Mart, Männik Andres, Kivi Gaily, Ustav Mart, Ustav Ene, Ustav Mart
Institute of Technology, University of Tartu, Tartu, Tartumaa, Estonia.
Icosagen Cell Factory OÜ, Ülenurme vald, Tartumaa, Estonia.
PLoS One. 2014 Dec 30;9(12):e116151. doi: 10.1371/journal.pone.0116151. eCollection 2014.
The human osteosarcoma cell line U2OS is useful for studying genome replication of human papillomavirus (HPVs) subtypes that belong to different phylogenetic genera. In this study, we defined the HPV18 transcription map in U2OS cells during transient replication, stable maintenance and vegetative amplification by identifying viral promoter regions, transcription polyadenylation and splicing sites during HPV18 genome replication. Mapping of the HPV18 transcription start sites in U2OS cells revealed five distinct promoter regions (P102, P520, P811, P1193 and P3000). With the exception of P3000, all of these regions have been previously identified during productive HPV18 infection. Collectively, the data suggest that U2OS cells are suitable for studying the replication and transcription properties of HPVs and to serve as a platform for conducting high-throughput drug screens to identify HPV replication inhibitors. In addition, we have identified mRNA species that are initiated from the promoter region P3000, which can encode two E2C regulator proteins that contain only the C-terminal hinge and DNA-binding and dimerization domains of E2. We show that these proteins regulate the initial amplification of HPV18 by modulating viral transcription. Moreover, we show that one of these proteins can act as a transcriptional activator of promoter P102.
人骨肉瘤细胞系U2OS对于研究属于不同系统发育属的人乳头瘤病毒(HPV)亚型的基因组复制很有用。在本研究中,我们通过在HPV18基因组复制过程中鉴定病毒启动子区域、转录聚腺苷酸化和剪接位点,确定了U2OS细胞在瞬时复制、稳定维持和营养扩增过程中的HPV18转录图谱。对U2OS细胞中HPV18转录起始位点的定位揭示了五个不同的启动子区域(P102、P520、P811、P1193和P3000)。除P3000外,所有这些区域先前在HPV18的有效感染过程中已被鉴定。总体而言,数据表明U2OS细胞适用于研究HPV的复制和转录特性,并可作为进行高通量药物筛选以鉴定HPV复制抑制剂的平台。此外,我们鉴定了从启动子区域P3000起始的mRNA种类,其可编码两种E2C调节蛋白,这些蛋白仅包含E2的C末端铰链区以及DNA结合和二聚化结构域。我们表明这些蛋白通过调节病毒转录来调控HPV18的初始扩增。此外,我们表明这些蛋白之一可作为启动子P102的转录激活因子。