Tsao Y P, Li L Y, Tsai T C, Chen S L
Department of Microbiology and Immunology, National Defense Medical Center, Taipei, Taiwan, Republic of China.
J Virol. 1996 Nov;70(11):7535-9. doi: 10.1128/JVI.70.11.7535-7539.1996.
Here we report that the E5 proteins of human papillomavirus type 11 (HPV-11) and HPV-16 suppressed the expression of the p21(WafI/SdiI/CipI) tumor suppressor gene in NIH 3T3 cells and immortalized human keratinocytes. The promoter activity of p21 was repressed by E5 of HPV-11 and -16, suggesting that p21 gene suppression by E5 was at the transcriptional level. Using an inducible system, we demonstrated that increased induction of HPV-11 E5 in NIH 3T3 cells and keratinocytes led to increased repression of p21 promoter activity. The repression of p21 promoter activity by a series of E5 mutants was somewhat correlated with their respective transforming activities. Previously, we and other investigators showed that the E5 proteins of HPV-11 and -16 can activate the expression of c-jun. The repression of p21 gene expression might be a mechanism of oncogene-mediated growth promotion, since the expression of c-jun also led to a reduction of the levels of p21 RNA and protein in keratinocytes. This is the first demonstration that E5 proteins of HPV-11 and -16 repress p21 gene expression, and this might be one of the mechanisms by which E5 stimulates cell proliferation. In addition, this is also the first report of c-jun repression of p21.
在此我们报告,人乳头瘤病毒11型(HPV-11)和HPV-16的E5蛋白在NIH 3T3细胞和永生化人角质形成细胞中抑制了肿瘤抑制基因p21(WafI/SdiI/CipI)的表达。HPV-11和-16的E5抑制了p21的启动子活性,这表明E5对p21基因的抑制作用发生在转录水平。利用诱导系统,我们证明,在NIH 3T3细胞和角质形成细胞中HPV-11 E5诱导的增加导致p21启动子活性的抑制增强。一系列E5突变体对p21启动子活性的抑制作用与其各自的转化活性有一定相关性。此前,我们和其他研究者表明,HPV-11和-16的E5蛋白可激活c-jun的表达。p21基因表达的抑制可能是癌基因介导的生长促进机制之一,因为c-jun的表达也导致角质形成细胞中p21 RNA和蛋白水平的降低。这是首次证明HPV-11和-16的E5蛋白抑制p21基因表达,这可能是E5刺激细胞增殖的机制之一。此外,这也是关于c-jun抑制p21的首次报道。