后期促进复合物
细胞周期蛋白B
细胞周期蛋白A2
细胞生物学
细胞周期蛋白
CDC20型
细胞周期蛋白D
细胞周期蛋白B1
主轴检查点
后期
G2-M DNA损伤检查点
中期
生物
化学
细胞周期检查点
细胞周期蛋白
细胞周期
主轴装置
细胞周期蛋白依赖激酶1
生物化学
细胞分裂
磷酸化
蛋白激酶A
细胞
基因
染色体
细胞周期蛋白依赖激酶2
作者
Stephan Geley,Edgar R. Kramer,Christian Gieffers,Julian Gannon,Jan‐Michael Peters,Tim Hunt
标识
DOI:10.1083/jcb.153.1.137
摘要
Cyclin A is a stable protein in S and G2 phases, but is destabilized when cells enter mitosis and is almost completely degraded before the metaphase to anaphase transition. Microinjection of antibodies against subunits of the anaphase-promoting complex/cyclosome (APC/C) or against human Cdc20 (fizzy) arrested cells at metaphase and stabilized both cyclins A and B1. Cyclin A was efficiently polyubiquitylated by Cdc20 or Cdh1-activated APC/C in vitro, but in contrast to cyclin B1, the proteolysis of cyclin A was not delayed by the spindle assembly checkpoint. The degradation of cyclin B1 was accelerated by inhibition of the spindle assembly checkpoint. These data suggest that the APC/C is activated as cells enter mitosis and immediately targets cyclin A for degradation, whereas the spindle assembly checkpoint delays the degradation of cyclin B1 until the metaphase to anaphase transition. The “destruction box” (D-box) of cyclin A is 10–20 residues longer than that of cyclin B. Overexpression of wild-type cyclin A delayed the metaphase to anaphase transition, whereas expression of cyclin A mutants lacking a D-box arrested cells in anaphase.
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