Wang Qing, Moyret-Lalle Caroline, Couzon Florence, Surbiguet-Clippe Christine, Saurin Jean-Christophe, Lorca Thierry, Navarro Claudine, Puisieux Alain
Centre d'Oncologie Génetique, INSERM U 453, Centre Léon Bérard, Lyon, France.
Oncogene. 2003 Mar 13;22(10):1486-90. doi: 10.1038/sj.onc.1206224.
Ubiquitin-mediated proteolysis of cell cycle regulators is a major element of the cell cycle control. The anaphase-promoting complex (APC/C) is a large multisubunit ubiquitin-protein ligase required for the ubiquitination and degradation of G1 and mitotic checkpoint regulators. APC/C-dependent proteolysis regulates cyclin levels in G1, and triggers the separation of sister chromatids at the metaphase-anaphase transition and the destruction of mitotic cyclins at the end of mitosis. Furthermore, it was recently shown that APC/C regulates the degradation of crucial regulators of signal transduction pathways. We report here gene alterations in several components of this complex in human colon cancer cells, including APC6/CDC16 and APC8/CDC23 which are known to be key function elements. The experimental expression of a truncation mutant of APC8/CDC23 subunit (CDC23DeltaTPR) leads to abnormal levels of APC/C targets such as cyclin B1 and disturbs the cell cycle progression of colon epithelial cells through mitosis. Overall, these data support the hypothesis of a deleterious role of these mutations during colorectal carcinogenesis.
泛素介导的细胞周期调节因子的蛋白水解是细胞周期控制的一个主要因素。后期促进复合物(APC/C)是一种大型多亚基泛素蛋白连接酶,是G1期和有丝分裂检查点调节因子的泛素化和降解所必需的。依赖APC/C的蛋白水解调节G1期的细胞周期蛋白水平,并在中期-后期转换时触发姐妹染色单体的分离以及在有丝分裂末期破坏有丝分裂细胞周期蛋白。此外,最近有研究表明,APC/C调节信号转导通路关键调节因子的降解。我们在此报告人类结肠癌细胞中该复合物几个组分的基因改变,包括已知为关键功能元件的APC6/CDC16和APC8/CDC23。APC8/CDC23亚基截短突变体(CDC23DeltaTPR)的实验性表达导致细胞周期蛋白B1等APC/C靶标的水平异常,并扰乱结肠上皮细胞通过有丝分裂的细胞周期进程。总体而言,这些数据支持了这些突变在结直肠癌发生过程中起有害作用的假说。