Walker D H, DePaoli-Roach A A, Maller J L
Howard Hughes Medical Institute, University of Colorado School of Medicine, Denver 80262.
Mol Biol Cell. 1992 Jun;3(6):687-98. doi: 10.1091/mbc.3.6.687.
Using cytostatic factor metaphase II-arrested extracts as a model system, we show that protein phosphatase 1 is regulated during early embryonic cell cycles in Xenopus. Phosphatase 1 activity peaks during interphase and decreases shortly before the onset of mitosis. A second peak of activity appears in mitosis at about the same time that cdc2 becomes active. If extracts are inhibited in S-phase with aphidicolin, then phosphatase 1 activity remains high. The activity of phosphatase 1 appears to determine the timing of exit from S-phase and entry into M-phase; inhibition of phosphatase 1 by the specific inhibitor, inhibitor 2 (Inh-2), causes premature entry into mitosis, whereas exogenously added phosphatase 1 lengthens the interphase period. Analysis of DNA synthesis in extracts treated with Inh-2, but lacking the A- and B-type cyclins, shows that phosphatase 1 is also required for the process of DNA replication. These data indicate that phosphatase 1 is a component of the signaling pathway that ensures that M-phase is not initiated until DNA synthesis is complete.
我们以细胞静止因子中期 II 阻滞提取物作为模型系统,证明了爪蟾早期胚胎细胞周期中蛋白磷酸酶 1 受到调控。磷酸酶 1 的活性在间期达到峰值,并在有丝分裂开始前不久下降。第二个活性峰值出现在有丝分裂期,与 cdc2 激活的时间大致相同。如果在 S 期用阿非迪霉素抑制提取物,那么磷酸酶 1 的活性会保持较高水平。磷酸酶 1 的活性似乎决定了退出 S 期并进入 M 期的时间;特异性抑制剂抑制剂 2(Inh - 2)抑制磷酸酶 1 会导致过早进入有丝分裂,而外源添加磷酸酶 1 则会延长间期。对用 Inh - 2 处理但缺乏 A 型和 B 型细胞周期蛋白的提取物中的 DNA 合成进行分析表明,DNA 复制过程也需要磷酸酶 1。这些数据表明,磷酸酶 1 是信号通路的一个组成部分,可确保在 DNA 合成完成之前不启动 M 期。