Tyers M, Jorgensen P
Programme in Molecular Biology and Cancer, Graduate Department of Molecular and Medical Genetics, Samuel Lunenfeld Research Institute, Mount Sinai Hospital, University of Toronto, Toronto, M5G 1X5, M5S 1A8, Canada.
Curr Opin Genet Dev. 2000 Feb;10(1):54-64. doi: 10.1016/s0959-437x(99)00049-0.
The ubiquitin system drives the cell division cycle by the timely destruction of numerous regulatory proteins. Remarkably, the two main activities that catalyze substrate ubiquitination in the cell cycle, the Skp1-Cdc53/cullin-F-box protein (SCF) complexes and the anaphase-promoting complex/cyclosome (APC/C), define a new superfamily of E3 ubiquitin ligases, all based on related cullin and RING-H2 finger protein subunits. The circuits that interconnect the SCF, APC/C and cyclin-dependent kinase activities form a master oscillator that coordinates the replication and segregation of the genome.
泛素系统通过及时降解众多调节蛋白来驱动细胞分裂周期。值得注意的是,在细胞周期中催化底物泛素化的两个主要活性成分,即Skp1-Cdc53/类cullin-F盒蛋白(SCF)复合物和后期促进复合物/细胞周期体(APC/C),定义了一个新的E3泛素连接酶超家族,它们均基于相关的类cullin和RING-H2指蛋白亚基。将SCF、APC/C和细胞周期蛋白依赖性激酶活性相互连接的信号通路形成了一个主振荡器,该振荡器协调基因组的复制和分离。