Department of Pharmacology and Cancer Biology, Duke University Schoolof Medicine, Durham, North Carolina, USA.
Prog Mol Biol Transl Sci. 2012;106:327-41. doi: 10.1016/B978-0-12-396456-4.00008-0.
Entry into and progression through mitosis depends critically on the establishment and maintenance of protein phosphorylation. For this reason, studies on mitotic progression have focused heavily on the activation of MPF (M phase promoting factor), a cyclin-dependent kinase responsible for phosphorylating proteins that execute the dynamic events of mitosis. Recent work, however, has significantly expanded our understanding of mechanisms that allow accumulation of phosphoproteins at M phase, suggesting that mitotic entry relies not only on MPF activation but also on the inhibition of antimitotic phosphatases. It is now clear that there exists a separate, albeit equally important, signaling pathway for the inactivation of protein phosphatases at the G2/M transition. This pathway, which is governed by the kinase Greatwall is essential for both entry into and maintenance of M phase. This chapter will outline the molecular events regulating entry into mitosis, specifically highlighting the role that protein phosphorylation plays in triggering both MPF activation and the inhibition of phosphatase activity that would otherwise prevent accumulation of mitotic phosphoproteins. These intricate regulatory pathways are essential for maintaining normal cell division and preventing inappropriate cell proliferation, a central hallmark of cancer cells.
有丝分裂的进入和进程取决于蛋白质磷酸化的建立和维持。出于这个原因,有丝分裂进程的研究主要集中在 MPF(M 期促进因子)的激活上,MPF 是一种细胞周期蛋白依赖性激酶,负责磷酸化执行有丝分裂动态事件的蛋白质。然而,最近的工作极大地扩展了我们对允许 M 期磷酸蛋白积累的机制的理解,表明有丝分裂的进入不仅依赖于 MPF 的激活,还依赖于抗有丝分裂磷酸酶的抑制。现在很清楚,在 G2/M 转换时,蛋白磷酸酶的失活存在一个单独的、但同样重要的信号通路。这条由激酶 Greatwall 控制的通路对于有丝分裂的进入和维持都是必不可少的。本章将概述调节有丝分裂进入的分子事件,特别强调蛋白质磷酸化在触发 MPF 激活和抑制磷酸酶活性方面的作用,否则磷酸酶活性会阻止有丝分裂磷酸蛋白的积累。这些复杂的调控途径对于维持正常的细胞分裂和防止不适当的细胞增殖至关重要,细胞增殖是癌细胞的一个中心特征。