Huang Xingxu, Tran Thanh, Zhang Lingna, Hatcher Rashieda, Zhang Pumin
Department of Molecular Physiology, Baylor College of Medicine, Houston, TX 77030, USA.
Proc Natl Acad Sci U S A. 2005 Jan 25;102(4):1065-70. doi: 10.1073/pnas.0409130102. Epub 2005 Jan 13.
Mitotic catastrophe is the response of mammalian cells to mitotic DNA damage. It produces tetraploid cells with a range of different nuclear morphologies from binucleated to multimicronucleated. In response to DNA damage, checkpoints are activated to delay cell cycle progression and to coordinate repair. Cells in different cell cycle phases use different mechanisms to arrest their cell cycle progression. It has remained unclear whether the termination of mitosis in a mitotic catastrophe is regulated by DNA damage checkpoints. Here, we report the presence of a mitotic exit DNA damage checkpoint in mammalian cells. This checkpoint delays mitotic exit and prevents cytokinesis and, thereby, is responsible for mitotic catastrophe. The DNA damage-induced mitotic exit delay correlates with the inhibition of Cdh1 activation and the attenuated degradation of cyclin B1. We demonstrate that the checkpoint is Chk1-dependent.
有丝分裂灾难是哺乳动物细胞对有丝分裂期DNA损伤的反应。它会产生具有一系列不同核形态的四倍体细胞,从双核到多核。作为对DNA损伤的反应,细胞周期检查点被激活,以延迟细胞周期进程并协调修复。处于不同细胞周期阶段的细胞使用不同机制来阻止其细胞周期进程。目前尚不清楚在有丝分裂灾难中,有丝分裂的终止是否受DNA损伤检查点的调控。在此,我们报告在哺乳动物细胞中存在一个有丝分裂退出DNA损伤检查点。这个检查点延迟有丝分裂退出并阻止胞质分裂,因此,它导致了有丝分裂灾难。DNA损伤诱导的有丝分裂退出延迟与Cdh1激活的抑制以及细胞周期蛋白B1降解的减弱相关。我们证明该检查点依赖于Chk1。