Zarzov Patrick, Decottignies Anabelle, Baldacci Giuseppe, Nurse Paul
Cancer Research UK London Research Institute, 44 Lincoln's Inn Fields, London WC2A 3PX, UK.
EMBO J. 2002 Jul 1;21(13):3370-6. doi: 10.1093/emboj/cdf346.
Cyclin-dependent kinase (CDK) Tyr15 phosphorylation plays a major role in regulating G(2)/M CDKs, but the role of this phosphorylation in regulating G(1)/S CDKs is less clear. We have studied the regulation and function of Cdc2-Tyr15 phosphorylation in the fission yeast Schizosaccharomyces pombe G(1)/S CDK Cig2/Cdc2. This complex is subject to high level Cdc2-Tyr15 phosphorylation inhibiting its kinase activity in hydroxyurea-treated cells blocked in S-phase. We show that this Tyr15 phosphorylation is required to maintain efficient mitotic checkpoint arrest, because Cig2 accumulates during the block and this accumulation can advance mitotic onset. This mitotic induction operates, at least in part, through activation of the normal G(2)/M CDK complex Cdc13/Cdc2. Thus, Tyr15 phosphorylation of G(1)/S CDK complexes is important in the checkpoint control blocking mitotic onset when DNA replication is inhibited.
细胞周期蛋白依赖性激酶(CDK)酪氨酸15位点的磷酸化在调节G(2)/M期CDK中起主要作用,但这种磷酸化在调节G(1)/S期CDK中的作用尚不清楚。我们研究了粟酒裂殖酵母G(1)/S期CDK Cig2/Cdc2中Cdc2-酪氨酸15位点磷酸化的调节及其功能。在被羟基脲处理而阻断在S期的细胞中,该复合物会发生高水平的Cdc2-酪氨酸15位点磷酸化,从而抑制其激酶活性。我们发现,这种酪氨酸15位点的磷酸化对于维持有效的有丝分裂检查点阻滞是必需的,因为在阻滞过程中Cig2会积累,并且这种积累会促进有丝分裂的开始。这种有丝分裂诱导至少部分是通过激活正常的G(2)/M期CDK复合物Cdc13/Cdc2来实现的。因此,当DNA复制受到抑制时,G(1)/S期CDK复合物的酪氨酸15位点磷酸化在阻止有丝分裂开始的检查点控制中起重要作用。