Bernard B A, Bailly C, Lenoir M C, Darmon M, Thierry F, Yaniv M
Centre International de Recherches Dermatologiques Sophia Antipolis, Valbonne, France.
J Virol. 1989 Oct;63(10):4317-24. doi: 10.1128/JVI.63.10.4317-4324.1989.
The human papillomavirus type 18 (HPV18) long control region (LCR) harbors transcriptional promoter and enhancer elements. Recombinant plasmids bearing all or part of the HPV18 LCR cloned in enhancer or promoter configuration upstream of the chloramphenicol acetyltransferase (CAT) gene were transfected into human fibroblasts and keratinocytes. Although the HPV18 enhancer can function in the absence of E2 gene products in both fibroblasts and keratinocytes, the promoter activity of the HPV18 LCR is detectable in keratinocytes but not in fibroblasts, suggesting that it is tissue specific. This promoter activity was repressed in human keratinocytes not only by the bovine papillomavirus type 1 E2 gene product but also by the homologous HPV18 E2 gene product. The promoter involved in the HPV18 E2 repression is located within a 230-base-pair domain directly upstream of the E6 open reading frame of the HPV18 LCR and is probably the previously identified E6 promoter. Although one cannot rule out the possibility that this repressing effect is mediated by a truncated form of HPV18 E2 protein, as was previously demonstrated for bovine papillomavirus type 1, a more likely explanation would be that the full-length HPV18 E2 protein behaves as a repressor. Indeed, at the same doses at which it inhibits transcription from the homologous HPV18 LCR, the HPV18 E2 gene product activates transcription from constructs bearing E2-binding palindromes cloned in enhancer configuration upstream of a heterologous promoter. The fact that the homologous HPV18 E2 gene product acts as a transcriptional repressor of the HPV18 LCR suggests a possible explanation for the overexpression of E6 and E7 open reading frames in cervical carcinoma cells and in cell lines derived from them.
人乳头瘤病毒18型(HPV18)长控制区(LCR)含有转录启动子和增强子元件。将携带全部或部分HPV18 LCR且以增强子或启动子构型克隆于氯霉素乙酰转移酶(CAT)基因上游的重组质粒转染至人成纤维细胞和角质形成细胞。虽然HPV18增强子在成纤维细胞和角质形成细胞中均可在无E2基因产物的情况下发挥作用,但HPV18 LCR的启动子活性在角质形成细胞中可检测到,而在成纤维细胞中则检测不到,这表明其具有组织特异性。这种启动子活性在人角质形成细胞中不仅受到牛乳头瘤病毒1型E2基因产物的抑制,也受到同源HPV18 E2基因产物的抑制。参与HPV18 E2抑制作用的启动子位于HPV18 LCR的E6开放阅读框直接上游的一个230碱基对结构域内,可能就是先前鉴定的E6启动子。虽然不能排除这种抑制作用是由HPV18 E2蛋白的截短形式介导的可能性,正如先前对牛乳头瘤病毒1型所证明的那样,但更可能的解释是全长HPV18 E2蛋白起阻遏物的作用。实际上,在抑制同源HPV18 LCR转录的相同剂量下,HPV18 E2基因产物可激活来自携带以增强子构型克隆于异源启动子上游的E2结合回文序列的构建体的转录。同源HPV18 E2基因产物作为HPV18 LCR的转录阻遏物这一事实,为子宫颈癌细胞及其衍生的细胞系中E6和E7开放阅读框的过表达提供了一种可能的解释。