The E6 oncoprotein encoded by human papillomavirus types 16 and 18 promotes the degradation of p53.

IF 42.5 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Cell Pub Date : 1990-12-21 DOI:10.1016/0092-8674(90)90409-8
M Scheffner, B A Werness, J M Huibregtse, A J Levine, P M Howley
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引用次数: 3969

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.

由16型和18型人乳头瘤病毒编码的E6癌蛋白促进p53的降解。
由致瘤性人乳头瘤病毒16型和18型编码的E6蛋白是hpv相关癌症中表达的两种病毒产物之一。E6是一种癌蛋白,与E7合作使原代人角质形成细胞永生化。通过观察HPV-16和HPV-18编码的E6蛋白可以在体外复合野生型p53蛋白,我们对E6在肿瘤发生中的作用机制有了进一步的了解。野生型p53基因具有肿瘤抑制特性,是DNA肿瘤病毒编码的几种癌蛋白的靶标。在这项研究中,我们证明了与p53结合的致癌hpv的E6蛋白刺激p53的降解。e6促进的p53降解是ATP依赖的,涉及泛素依赖的蛋白酶系统。具有负调控功能的细胞蛋白(如p53)的选择性降解为显性癌蛋白提供了一种新的作用机制。
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来源期刊
Cell
Cell 生物-生化与分子生物学
CiteScore
110.00
自引率
0.80%
发文量
396
审稿时长
2 months
期刊介绍: Cells is an international, peer-reviewed, open access journal that focuses on cell biology, molecular biology, and biophysics. It is affiliated with several societies, including the Spanish Society for Biochemistry and Molecular Biology (SEBBM), Nordic Autophagy Society (NAS), Spanish Society of Hematology and Hemotherapy (SEHH), and Society for Regenerative Medicine (Russian Federation) (RPO). The journal publishes research findings of significant importance in various areas of experimental biology, such as cell biology, molecular biology, neuroscience, immunology, virology, microbiology, cancer, human genetics, systems biology, signaling, and disease mechanisms and therapeutics. The primary criterion for considering papers is whether the results contribute to significant conceptual advances or raise thought-provoking questions and hypotheses related to interesting and important biological inquiries. In addition to primary research articles presented in four formats, Cells also features review and opinion articles in its "leading edge" section, discussing recent research advancements and topics of interest to its wide readership.
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