Laboratory of Biosignaling & Therapeutics, Department of Molecular Cell Biology, University of Leuven, B-3000 Leuven, Belgium.
Trends Cell Biol. 2009 Oct;19(10):531-41. doi: 10.1016/j.tcb.2009.06.005. Epub 2009 Sep 4.
While the importance of protein kinases for the spatial and temporal control of mitotic events has long been recognized, mitotic phosphatases have only recently come into the limelight. It is now well established that protein phosphatases counteract mitotic kinases, so contributing to the generation of switch-like responses at mitotic stage transitions. In addition, the timely dephosphorylation of mitotic phosphoproteins by tightly regulated phosphatases is required for the assembly and stability of the mitotic spindle, the initiation of anaphase, and exit from mitosis. Mitotic phosphatases also emerge as effectors of the DNA damage and spindle assembly checkpoints. These new findings show that protein phosphatases regulate every step of mitosis and provide novel insights into the dynamic and versatile nature of mitotic phosphoregulation.
虽然蛋白激酶对于有丝分裂事件的时空控制的重要性早已被认识,但有丝分裂磷酸酶直到最近才受到关注。现在已经确定,蛋白磷酸酶与有丝分裂激酶相互作用,因此有助于在有丝分裂阶段转换时产生类似开关的反应。此外,有丝分裂磷酸蛋白通过受严格调控的磷酸酶进行及时去磷酸化,对于有丝分裂纺锤体的组装和稳定性、后期起始以及有丝分裂退出都是必需的。有丝分裂磷酸酶也作为 DNA 损伤和纺锤体组装检查点的效应物出现。这些新发现表明,蛋白磷酸酶调节有丝分裂的每一步,并为有丝分裂磷酸调节的动态和多功能性质提供了新的见解。