生物
癌变
抑制器
泛素
基因
泛素连接酶
细胞生物学
抑癌基因
机制(生物学)
肿瘤病毒
人乳头瘤病毒
癌症研究
病毒学
遗传学
病毒
医学
哲学
认识论
内科学
作者
Martin Scheffner,Bruce A. Werness,Jon M. Huibregtse,Arnold J. Levine,Peter M. Howley
出处
期刊:Cell
[Cell Press]
日期:1990-12-01
卷期号:63 (6): 1129-1136
被引量:3919
标识
DOI:10.1016/0092-8674(90)90409-8
摘要
Abstract
The E6 protein encoded by the oncogenic human papillomavirus types 16 and 18 is one of two viral products expressed in HPV-associated cancers. E6 is an oncoprotein which cooperates with E7 to immortalize primary human keratinocytes. Insight into the mechanism by which E6 functions in oncogenesis is provided by the observation that the E6 protein encoded by HPV-16 and HPV-18 can complex the wild-type p53 protein in vitro. Wild-type p53 gene has tumor suppressor properties, and is a target for several of the oncoproteins encoded by DNA tumor viruses. In this study we demonstrate that the E6 proteins of the oncogenic HPVs that bind p53 stimulate the degradation of p53. The E6-promoted degradation of p53 is ATP dependent and involves the ubiquitin-dependent protease system. Selective degradation of cellular proteins such as p53 with negative regulatory functions provides a novel mechanism of action for dominant-acting oncoproteins.
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