Liu Hong, Wang Yanchang
Department of Biomedical Sciences, College of Medicine, Florida State University, Tallahassee, FL 32306, USA.
Mol Biol Cell. 2006 Jun;17(6):2746-56. doi: 10.1091/mbc.e05-11-1093. Epub 2006 Mar 29.
Periodically regulated cyclin-dependent kinase (Cdk) is required for DNA synthesis and mitosis. Hydroxyurea (HU) inhibits DNA synthesis by depleting dNTPs, the basic unit for DNA synthesis. HU treatment triggers the S-phase checkpoint, which arrests cells at S-phase, inhibits late origin firing and stabilizes replication forks. Using budding yeast as a model system, we found that Swe1, a negative regulator of Cdk, appears at S-phase and accumulates in HU treatment cells. Interestingly, this accumulation is not dependent on S-phase checkpoint. Deltahsl1, Deltahsl7, and cdc5-2 mutants, which have defects in Swe1 degradation, show HU sensitivity because of high Swe1 protein levels. We further demonstrated that their HU sensitivity is not a result of DNA damage accumulation or incomplete DNA synthesis; instead the sensitivity is due to their dramatically delayed recovery from HU-induced S-phase arrest. Strikingly, our in vivo data indicate that Swe1 inhibits the kinase activity of Clb2-Cdk1, but not that of Clb5-Cdk1. Therefore, S-phase accumulated Swe1 prevents Clb2-Cdk1-mediated mitotic activities, but has little effects on Clb5-Cdk1-associated S-phase progression.
周期性调控的细胞周期蛋白依赖性激酶(Cdk)是DNA合成和有丝分裂所必需的。羟基脲(HU)通过消耗DNA合成的基本单位dNTP来抑制DNA合成。HU处理会触发S期检查点,使细胞停滞在S期,抑制晚期起始点激发并稳定复制叉。以芽殖酵母作为模型系统,我们发现Cdk的负调控因子Swe1出现在S期并在HU处理的细胞中积累。有趣的是,这种积累不依赖于S期检查点。在Swe1降解方面存在缺陷的Deltahsl1、Deltahsl7和cdc5-2突变体,由于Swe1蛋白水平较高而表现出对HU的敏感性。我们进一步证明,它们对HU的敏感性不是DNA损伤积累或DNA合成不完全的结果;相反,这种敏感性是由于它们从HU诱导的S期停滞中恢复的时间显著延迟。引人注目的是,我们的体内数据表明,Swe1抑制Clb2-Cdk1的激酶活性,但不抑制Clb5-Cdk1的激酶活性。因此,S期积累的Swe1可防止Clb2-Cdk1介导的有丝分裂活动,但对Clb5-Cdk1相关的S期进程影响很小。