Guadagno T M, Ferrell J E
Department of Molecular Pharmacology, Stanford University School of Medicine, Stanford, CA 94305-5332, USA.
Science. 1998 Nov 13;282(5392):1312-5. doi: 10.1126/science.282.5392.1312.
The p42 mitogen-activated protein kinase (MAPK) is required for progression through meiotic M phase in Xenopus oocytes. This report examines whether it also plays a role in normal mitotic progression. MAPK was transiently activated during mitosis in cycling Xenopus egg extracts after activation of the cyclin-dependent kinase Cdc2-cyclin B. Interference with MAPK activation by immunodepletion of its activator MEK, or by addition of the MEK inhibitor PD98059, caused precocious termination of mitosis and interfered with production of normal mitotic microtubules. Sustained activation of MAPK arrested extracts in mitosis in the absence of active Cdc2-cyclin B. These findings identify a role for MEK and MAPK in maintaining the mitotic state.
非洲爪蟾卵母细胞减数分裂M期的进程需要p42丝裂原活化蛋白激酶(MAPK)。本报告研究了它在正常有丝分裂进程中是否也发挥作用。在细胞周期蛋白依赖性激酶Cdc2 - 细胞周期蛋白B激活后,非洲爪蟾卵提取物在有丝分裂过程中MAPK会短暂激活。通过免疫去除其激活剂MEK或添加MEK抑制剂PD98059来干扰MAPK激活,会导致有丝分裂过早终止,并干扰正常有丝分裂微管的产生。在没有活性Cdc2 - 细胞周期蛋白B的情况下,MAPK的持续激活会使提取物停滞在有丝分裂期。这些发现确定了MEK和MAPK在维持有丝分裂状态中的作用。