Veldman T, Horikawa I, Barrett J C, Schlegel R
Departments of Pathology and Oncology, Georgetown University Medical School, Washington, D.C. 20007, USA.
J Virol. 2001 May;75(9):4467-72. doi: 10.1128/JVI.75.9.4467-4472.2001.
The E6 and E7 oncogenes of human papillomavirus type 16 (HPV-16) are sufficient for the immortalization of human genital keratinocytes in vitro. The products of these viral genes associate with p53 and pRb tumor suppressor proteins, respectively, and interfere with their normal growth-regulatory functions. The HPV-16 E6 protein has also been shown to increase the telomerase enzyme activity in primary epithelial cells by an unknown mechanism. We report here that a study using reverse transcription-PCR and RNase protection assays in transduced primary human foreskin keratinocytes (HFKs) shows that the E6 gene (but not the E7 gene) increases telomerase hTERT gene transcription coordinately with E6-induced telomerase activity. In these same cells, the E6 gene induces a 6.5-fold increase in the activity of a 1,165-bp 5' promoter/regulatory region of the hTERT gene, and this induction is attributable to a minimal 251-bp sequence (-211 to +40). Furthermore, there is a 35-bp region (+5 to +40) within this minimal E6-responsive promoter that is responsible for 60% of E6 activity. Although the minimal hTERT promoter contains Myc-responsive E-box elements and recent studies have suggested a role for Myc protein in hTERT transcriptional control, we found no alterations in the abundance of either c-Myc or c-Mad in E6-transduced HFKs, suggesting that there are other or additional transcription factors critical for regulating hTERT expression.
人乳头瘤病毒16型(HPV - 16)的E6和E7癌基因足以使人泌尿生殖系统角质形成细胞在体外永生化。这些病毒基因的产物分别与p53和pRb肿瘤抑制蛋白结合,并干扰它们正常的生长调节功能。HPV - 16 E6蛋白还被证明可通过未知机制提高原代上皮细胞中的端粒酶活性。我们在此报告,一项在转导的原代人包皮角质形成细胞(HFK)中使用逆转录 - PCR和核糖核酸酶保护分析的研究表明,E6基因(而非E7基因)与E6诱导的端粒酶活性协同增加端粒酶hTERT基因转录。在这些相同的细胞中,E6基因使hTERT基因1165 bp的5'启动子/调控区域的活性增加6.5倍,这种诱导归因于最小的251 bp序列(-211至+40)。此外,在这个最小的E6反应性启动子内有一个35 bp区域(+5至+40),它负责E6活性的60%。尽管最小的hTERT启动子包含Myc反应性E - 盒元件,并且最近的研究表明Myc蛋白在hTERT转录控制中起作用,但我们发现在E6转导的HFK中c - Myc或c - Mad的丰度没有改变,这表明存在其他或额外的对调节hTERT表达至关重要的转录因子。