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SCF 型泛素连接酶对细胞周期的调控。

Regulation of the cell cycle by SCF-type ubiquitin ligases.

作者信息

Nakayama Keiichi I, Nakayama Keiko

机构信息

Department of Molecular and Cellular Biology, Medical Institute of Bioregulation, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka, Fukuoka 812-8582, Japan.

出版信息

Semin Cell Dev Biol. 2005 Jun;16(3):323-33. doi: 10.1016/j.semcdb.2005.02.010.

Abstract

Regulation of the cell cycle is dependent on protein degradation by the ubiquitin-proteasome system. Two major ubiquitin ligases, the anaphase-promoting complex or cyclosome (APC/C) and SCF complex, are responsible for the periodic proteolysis of many regulators of the cell cycle. The receptor component of the SCF complex is one of many F-box proteins, three of which--Skp2, Fbw7, and beta-TrCP--are well characterized and implicated in cell cycle regulation. We have generated mice deficient in Skp2, Fbw7, or beta-TrCP1 and have identified the roles of these proteins in both cell cycle regulation and mouse development. Clinical evidence also suggests that dysregulation of these F-box proteins contributes to human cancers.

摘要

细胞周期的调控依赖于泛素 - 蛋白酶体系统介导的蛋白质降解。两种主要的泛素连接酶,后期促进复合物或周期体(APC/C)和SCF复合物,负责细胞周期许多调节因子的周期性蛋白水解。SCF复合物的受体成分是众多F - 盒蛋白之一,其中三种——Skp2、Fbw7和β-TrCP——已得到充分表征并与细胞周期调控有关。我们已培育出缺乏Skp2、Fbw7或β-TrCP1的小鼠,并确定了这些蛋白质在细胞周期调控和小鼠发育中的作用。临床证据还表明,这些F - 盒蛋白的失调与人类癌症有关。

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