King R W, Deshaies R J, Peters J M, Kirschner M W
Department of Cell Biology, Harvard Medical School, 240 Longwood Ave., Boston, MA 02115, USA.
Science. 1996 Dec 6;274(5293):1652-9. doi: 10.1126/science.274.5293.1652.
Oscillations in the activity of cyclin-dependent kinases (CDKs) promote progression through the eukaryotic cell cycle. This review examines how proteolysis regulates CDK activity-by degrading CDK activators or inhibitors-and also how proteolysis may directly trigger the transition from metaphase to anaphase. Proteolysis during the cell cycle is mediated by two distinct ubiquitin-conjugation pathways. One pathway, requiring CDC34, initiates DNA replication by degrading a CDK inhibitor. The second pathway, involving a large protein complex called the anaphase-promoting complex or cyclosome, initiates chromosome segregation and exit from mitosis by degrading anaphase inhibitors and mitotic cyclins. Proteolysis therefore drives cell cycle progression not only by regulating CDK activity, but by directly influencing chromosome and spindle dynamics.
细胞周期蛋白依赖性激酶(CDK)活性的振荡促进真核细胞周期的进程。本综述探讨了蛋白水解如何通过降解CDK激活剂或抑制剂来调节CDK活性,以及蛋白水解如何直接触发从中期到后期的转变。细胞周期中的蛋白水解由两条不同的泛素结合途径介导。一条途径需要CDC34,通过降解CDK抑制剂来启动DNA复制。第二条途径涉及一种称为后期促进复合物或细胞周期体的大型蛋白质复合物,通过降解后期抑制剂和有丝分裂细胞周期蛋白来启动染色体分离和有丝分裂退出。因此,蛋白水解不仅通过调节CDK活性来驱动细胞周期进程,还通过直接影响染色体和纺锤体动力学来实现。