Jones D L, Münger K
Department of Pathology, Harvard Medical School, Boston, Massachusetts 02115, USA.
J Virol. 1997 Apr;71(4):2905-12. doi: 10.1128/JVI.71.4.2905-2912.1997.
Cells expressing human papillomavirus type 16 (HPV-16) E7, similar to those which express HPV-16 E6, are resistant to a p53-mediated G1 growth arrest. We examined the p53-mediated DNA damage response pathway in E7-expressing cells to determine the mechanism by which E7-containing cells continue to cycle. In response to DNA damage, no dramatic difference was detected in G1- or S-phase cyclin or cyclin-dependent kinase (Cdk) levels when E7-expressing cells were compared to the parental cell line, RKO. Furthermore, Cdk2 kinase activity was inhibited in both RKO cells and E7-expressing cells, while Cdk2 remained active in E6-expressing cells. However, the steady-state levels of pRB and p107 protein were substantially lower in E7-expressing cells than in the parental RKO cells or E6-expressing cells. There was no reduction in pRB mRNA levels, but the half-life of pRB in E7-expressing cells was markedly shorter. Infection of primary human foreskin keratinocytes with recombinant retroviruses expressing HPV-16 E7 resulted in a decrease in pRB protein levels, indicating this phenomenon is a consequence of E7 expression, not of immortalization or transformation. These data strongly suggest E7 interferes with the stability of pRB and p107 protein. We propose that the removal of these components of the p53-mediated G1 growth arrest pathway in E7-expressing cells contributes to the ability of E7 to overcome a p53-mediated G1 growth arrest.
表达人乳头瘤病毒16型(HPV - 16)E7的细胞,类似于那些表达HPV - 16 E6的细胞,对p53介导的G1期生长停滞具有抗性。我们检测了表达E7的细胞中p53介导的DNA损伤反应途径,以确定含E7的细胞继续循环的机制。在DNA损伤反应中,将表达E7的细胞与亲代细胞系RKO相比,未检测到G1期或S期细胞周期蛋白或细胞周期蛋白依赖性激酶(Cdk)水平有显著差异。此外,Cdk2激酶活性在RKO细胞和表达E7的细胞中均受到抑制,而在表达E6的细胞中Cdk2仍保持活性。然而,表达E7的细胞中pRB和p107蛋白的稳态水平明显低于亲代RKO细胞或表达E6的细胞。pRB mRNA水平没有降低,但表达E7的细胞中pRB的半衰期明显缩短。用表达HPV - 16 E7的重组逆转录病毒感染原代人包皮角质形成细胞导致pRB蛋白水平降低,表明这种现象是E7表达的结果,而非永生化或转化的结果。这些数据强烈表明E7干扰了pRB和p107蛋白的稳定性。我们提出,在表达E7的细胞中去除p53介导的G1期生长停滞途径的这些成分有助于E7克服p53介导的G1期生长停滞的能力。