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人乳头瘤病毒16型和18型编码的E6癌蛋白可促进p53的降解。

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

作者信息

Scheffner M, Werness B A, Huibregtse J M, Levine A J, Howley P M

机构信息

Laboratory of Tumor Virus Biology, National Cancer Institute, Bethesda, Maryland 20892.

出版信息

Cell. 1990 Dec 21;63(6):1129-36. doi: 10.1016/0092-8674(90)90409-8.

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.

摘要

致癌性人乳头瘤病毒16型和18型所编码的E6蛋白是在人乳头瘤病毒相关癌症中表达的两种病毒产物之一。E6是一种癌蛋白,它与E7协同作用使原代人角质形成细胞永生化。人乳头瘤病毒16型和18型所编码的E6蛋白在体外可与野生型p53蛋白形成复合物,这一观察结果为深入了解E6在肿瘤发生中的作用机制提供了线索。野生型p53基因具有肿瘤抑制特性,是几种DNA肿瘤病毒所编码的癌蛋白的作用靶点。在本研究中,我们证明了与p53结合的致癌性人乳头瘤病毒的E6蛋白可刺激p53的降解。E6促进的p53降解依赖于ATP,并涉及泛素依赖性蛋白酶系统。对具有负调控功能的细胞蛋白(如p53)进行选择性降解,为显性作用癌蛋白提供了一种新的作用机制。

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