Morgan I M, Grindlay G J, Campo M S
Beatson Institute for Cancer Research, CRC Beatson Laboratories, Glasgow, UK.
J Gen Virol. 1998 Mar;79 ( Pt 3):501-8. doi: 10.1099/0022-1317-79-3-501.
Bovine papillomavirus 4 (BPV-4) is a mucosal epitheliotropic papillomavirus. It encodes a transcriptional regulator, E2, which acts on the BPV-4 transcriptional control region (the long control region or LCR) to regulate transcription. The distribution of E2 binding sites within the LCR of BPV-4 is identical to that of the human papillomaviruses HPV-16 and HPV-18, indicating that the mechanism of transcriptional control by E2 of mucosal epitheliotropic papillomaviruses is conserved. In this study it has been shown that E2 activates transcription through the BPV-4 LCR promoter in primary bovine palate keratinocytes but not in primary bovine palate fibroblasts. The epithelial specific transcriptional activation of the BPV-4 LCR by E2 is promoter-specific because following binding to the BPV-4 LCR placed in an enhancer mode, E2 can activate transcription from heterologous promoters, such as SV40, in both keratinocytes and fibroblasts. Chimaeric VP16-E2 molecules suggest that the epithelial specific transcriptional activation of the BPV-4 LCR promoter is mediated by the E2 transactivation domain. Although low to intermediate levels of E2 can activate transcription from the BPV-4 LCR promoter, high levels of E2 result in down-regulation of transcription from this promoter in keratinocytes. Mutation of E2 binding site 1 (BS1), which is 3 bp upstream from the TATA box, abrogates down-regulation of transcription by high levels of E2. The results present a model system for studying transcriptional regulation of mucosal epitheliotropic papillomavirus LCRs by E2.
牛乳头瘤病毒4型(BPV - 4)是一种嗜黏膜上皮的乳头瘤病毒。它编码一种转录调节因子E2,该因子作用于BPV - 4转录控制区(长控制区或LCR)以调节转录。BPV - 4的LCR内E2结合位点的分布与人类乳头瘤病毒HPV - 16和HPV - 18的相同,这表明嗜黏膜上皮乳头瘤病毒E2转录控制机制是保守的。在本研究中已表明,E2通过BPV - 4 LCR启动子在原代牛腭角质形成细胞中激活转录,但在原代牛腭成纤维细胞中则不然。E2对BPV - 4 LCR的上皮特异性转录激活是启动子特异性的,因为在与以增强子模式放置的BPV - 4 LCR结合后,E2可以在角质形成细胞和成纤维细胞中激活来自异源启动子(如SV40)的转录。嵌合的VP16 - E2分子表明,BPV - 4 LCR启动子的上皮特异性转录激活是由E2反式激活域介导的。虽然低至中等水平的E2可以激活BPV - 4 LCR启动子的转录,但高水平的E2会导致角质形成细胞中该启动子的转录下调。TATA框上游3 bp处的E2结合位点1(BS1)发生突变会消除高水平E2对转录的下调作用。这些结果提供了一个用于研究嗜黏膜上皮乳头瘤病毒LCRs由E2进行转录调控的模型系统。