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泛素-蛋白酶体途径与人类疾病的发病机制。

The ubiquitin-proteasome pathway and pathogenesis of human diseases.

作者信息

Schwartz A L, Ciechanover A

机构信息

Department of Pediatrics, Washington University School of Medicine, St. Louis, Missouri 63110, USA.

出版信息

Annu Rev Med. 1999;50:57-74. doi: 10.1146/annurev.med.50.1.57.

Abstract

The ubiquitin-proteasome pathway plays a pivotal role in the degradation of short-lived and regulatory proteins important in a variety of basic cellular processes, including regulation of the cell cycle, modulation of cell surface receptors and ion channels, and antigen presentation. The pathway involves an enzymatic cascade through which multiple ubiquitin molecules are covalently attached to the protein substrate, which is then degraded by the 26S proteasome complex. The pathway has been implicated in several forms of malignancy, in the pathogenesis of several genetic diseases (including cystic fibrosis, Angelman's syndrome, and Liddle syndrome), in immune surveillance/viral pathogenesis, and in the pathology of muscle wasting. The molecular mechanisms that underlie these processes are being unraveled at present.

摘要

泛素-蛋白酶体途径在多种基本细胞过程中对短命和调节蛋白的降解起着关键作用,这些过程包括细胞周期调控、细胞表面受体和离子通道的调节以及抗原呈递。该途径涉及一个酶促级联反应,通过该反应多个泛素分子共价连接到蛋白质底物上,然后由26S蛋白酶体复合物将其降解。该途径与多种恶性肿瘤形式、几种遗传疾病(包括囊性纤维化、天使综合征和利德尔综合征)的发病机制、免疫监视/病毒发病机制以及肌肉萎缩的病理学有关。目前正在揭示这些过程背后的分子机制。

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