Guadagno T M, Newport J W
Department of Biology, University of California, San Diego, La Jolla 92093-0347, USA.
Cell. 1996 Jan 12;84(1):73-82. doi: 10.1016/s0092-8674(00)80994-0.
In higher eukaryotes, Cdk2 kinase plays an essential role in regulating the G1-S transition. Here, we use cycling Xenopus egg extracts to examine the requirement of Cdk2 kinase on progression into mitosis. Interestingly, when Cdk2 kinase activity is inhibited by the Cdk-specific inhibitor, p21Cip1, a block to mitosis occurs, and inactive Cdc2-cyclin B accumulates. This block occurs in the absence of nuclei and is not due to direct inhibition of Cdc2 by Cip. Importantly, this block to mitosis is reversible by restoring Cdk2-cyclin E kinase activity to a Cip-treated cycling extract. Moreover, immunodepletion of Cdk2 from interphase extracts prevents activation of Cdc2 upon the addition of exogenous cyclin B. Thus, our data show that Cdk2 kinase is a positive regulator of Cdc2-cyclin B complexes and establish a link between Cdk2 kinase and cell cycle progression into mitosis.
在高等真核生物中,细胞周期蛋白依赖性激酶2(Cdk2)在调控G1期向S期的转变过程中发挥着至关重要的作用。在此,我们利用处于细胞周期循环的非洲爪蟾卵提取物来研究Cdk2激酶对于进入有丝分裂进程的必要性。有趣的是,当Cdk特异性抑制剂p21Cip1抑制Cdk2激酶活性时,会出现有丝分裂阻滞,并且无活性的细胞周期蛋白依赖性激酶2(Cdc2)-细胞周期蛋白B会积累。这种阻滞在没有细胞核的情况下也会发生,并且并非由于Cip直接抑制Cdc2所致。重要的是,通过将Cdk2-细胞周期蛋白E激酶活性恢复到经Cip处理的处于细胞周期循环的提取物中,这种有丝分裂阻滞是可逆的。此外,从间期提取物中免疫去除Cdk2会阻止在添加外源细胞周期蛋白B后Cdc2的激活。因此,我们的数据表明Cdk2激酶是Cdc2-细胞周期蛋白B复合物的正向调节因子,并在Cdk2激酶与进入有丝分裂的细胞周期进程之间建立了联系。