Huibregtse J M, Scheffner M, Howley P M
Laboratory of Tumor Virus Biology, National Cancer Institute, Bethesda, Maryland 20892.
Mol Cell Biol. 1993 Feb;13(2):775-84. doi: 10.1128/mcb.13.2.775-784.1993.
The E6 oncoproteins of the cancer-associated or high-risk human papillomaviruses (HPVs) target the cellular p53 protein. The association of E6 with p53 leads to the specific ubiquitination and degradation of p53 in vitro, suggesting a model by which E6 deregulates cell growth control by the elimination of the p53 tumor suppressor protein. Complex formation between E6 and p53 requires an additional cellular factor, designated E6-AP (E6-associated protein), which has a native and subunit molecular mass of approximately 100 kDa. Here we report the purification of E6-AP and the cloning of its corresponding cDNA, which contains a novel open reading frame encoding 865 amino acids. E6-AP, translated in vitro, has the following properties: (i) it associates with wild-type p53 in the presence of the HPV16 E6 protein and simultaneously stimulates the association of E6 with p53, (ii) it associates with the high-risk HPV16 and HPV18 E6 proteins in the absence of p53, and (iii) it induces the E6- and ubiquitin-dependent degradation of p53 in vitro.
癌症相关或高危型人乳头瘤病毒(HPV)的E6癌蛋白作用于细胞p53蛋白。E6与p53的结合导致p53在体外发生特异性泛素化和降解,提示了一种模型,即E6通过消除p53肿瘤抑制蛋白来解除对细胞生长的控制。E6与p53之间形成复合物需要另一种细胞因子,即E6相关蛋白(E6-AP),其天然亚基分子量约为100 kDa。在此我们报道了E6-AP的纯化及其相应cDNA的克隆,该cDNA含有一个编码865个氨基酸的新开放阅读框。体外翻译的E6-AP具有以下特性:(i)在HPV16 E6蛋白存在的情况下,它与野生型p53结合,同时刺激E6与p53的结合;(ii)在没有p53的情况下,它与高危型HPV16和HPV18 E6蛋白结合;(iii)它在体外诱导E6和泛素依赖性的p53降解。