Chen S L, Tsao Y P, Yang C M, Lin Y K, Huang C H, Kuo S W
Department of Microbiology and Immunology, National Defense Medical Center, Taipei, Taiwan, Republic of China.
J Gen Virol. 1995 Nov;76 ( Pt 11):2653-9. doi: 10.1099/0022-1317-76-11-2653.
The E5a gene of human papillomavirus type 11 (HPV-11) is a transforming oncogene. In this study, we investigated the mechanism of E5a induced transformation. Our results show that the expression of c-jun and junB, but not junD, was activated by HPV-11 E5a in NIH 3T3 cells and human epidermal keratinocytes. However, the expression of c-fos was activated by E5a in NIH 3T3 cells, but not in keratinocytes. We further investigated the mechanism of c-jun and junB induction by E5a. The amount of c-jun and junB RNAs correlated with the amount of E5a RNA in the heavy metal inducible system. E5a constitutively activated the expression of c-jun and junB at the initiation of transcription level. In addition, analyses of the effect of serum on c-jun expression in E5a transformed human epidermal keratinocytes show that EGF might have a stimulatory effect on c-jun gene expression in E5a expressing keratinocytes.
人乳头瘤病毒11型(HPV - 11)的E5a基因是一种具有转化作用的致癌基因。在本研究中,我们探究了E5a诱导转化的机制。我们的结果表明,在NIH 3T3细胞和人表皮角质形成细胞中,HPV - 11 E5a可激活c - jun和junB的表达,但不激活junD的表达。然而,E5a可在NIH 3T3细胞中激活c - fos的表达,但在角质形成细胞中则不然。我们进一步研究了E5a诱导c - jun和junB的机制。在重金属诱导系统中,c - jun和junB RNA的量与E5a RNA的量相关。E5a在转录起始水平组成性地激活c - jun和junB的表达。此外,对血清对E5a转化的人表皮角质形成细胞中c - jun表达的影响分析表明,表皮生长因子(EGF)可能对表达E5a的角质形成细胞中c - jun基因的表达具有刺激作用。