Oh S T, Kyo S, Laimins L A
Department of Microbiology-Immunology, Northwestern University Medical School, Chicago, Illinois 60611, USA.
J Virol. 2001 Jun;75(12):5559-66. doi: 10.1128/JVI.75.12.5559-5566.2001.
High-risk human papillomaviruses (HPVs) immortalize keratinocytes by disrupting the retinoblastoma protein (Rb)/p16 pathway and activating telomerase. The E7 oncoprotein targets Rb, while the E6 oncoprotein induces telomerase activity in human keratinocytes. This study has examined the mechanism by which E6 activates telomerase. Expression of human telomerase reverse transcriptase (hTERT), the catalytic subunit of telomerase, was found to be increased in keratinocytes stably expressing HPV type 16 E6, suggesting that E6 acts to increase hTERT transcription. hTERT expression and telomerase activity were activated to significantly higher levels in cells expressing both E6 and E7 than in cells expressing E6 alone. This indicates that E7 may augment E6-mediated activation of hTERT transcription. In transient-transfection assays using hTERT reporters, the induction of hTERT expression by E6 was found to be mediated by a 258-bp fragment of the hTERT promoter, proximal to the ATG initiation codon. Previous studies have demonstrated that overexpression of Myc can activate hTERT expression, suggesting that Myc may be a mediator of E6-mediated hTERT induction. However, in cells stably expressing E6, no strict correlation between the level of Myc and the activation of hTERT was found. Consistent with this observation, mutation of the two Myc binding sites in the hTERT promoter only modestly reduced responsiveness to E6 in transient reporter assays. This indicates that activation of Myc-dependent transcription is not essential for E6-mediated upregulation of hTERT expression. The hTERT promoter also contains five GC-rich elements that can bind Sp1. Mutation of these sites within the 258-bp fragment partially reduced hTERT induction by E6. However, when mutations in the Sp1 sites were combined with the mutated Myc binding sites, all activation by E6 was lost. This indicates that it is the combinatorial binding of factors to Myc and Sp1 cis elements that is responsible for hTERT induction by E6.
高危型人乳头瘤病毒(HPV)通过破坏视网膜母细胞瘤蛋白(Rb)/p16通路并激活端粒酶,使角质形成细胞永生化。E7癌蛋白作用于Rb,而E6癌蛋白可诱导人角质形成细胞中的端粒酶活性。本研究探讨了E6激活端粒酶的机制。在稳定表达16型HPV E6的角质形成细胞中,发现端粒酶的催化亚基人端粒酶逆转录酶(hTERT)的表达增加,这表明E6的作用是增加hTERT转录。与单独表达E6的细胞相比,同时表达E6和E7的细胞中hTERT表达和端粒酶活性被激活到显著更高的水平。这表明E7可能增强E6介导的hTERT转录激活。在使用hTERT报告基因的瞬时转染实验中,发现E6对hTERT表达的诱导作用是由hTERT启动子靠近ATG起始密码子的一段258 bp片段介导的。先前的研究表明,Myc的过表达可激活hTERT表达,这表明Myc可能是E6介导的hTERT诱导的介质。然而,在稳定表达E6的细胞中,未发现Myc水平与hTERT激活之间存在严格的相关性。与此观察结果一致,在瞬时报告基因实验中,hTERT启动子中两个Myc结合位点的突变仅适度降低了对E6的反应性。这表明Myc依赖性转录的激活对于E6介导的hTERT表达上调并非必不可少。hTERT启动子还包含五个可结合Sp1的富含GC的元件。在258 bp片段内这些位点的突变部分降低了E6对hTERT的诱导作用。然而,当Sp1位点的突变与突变的Myc结合位点结合时,E6的所有激活作用均丧失。这表明是因子与Myc和Sp1顺式元件的组合结合导致了E6对hTERT的诱导。