Zhu Yonghong, Alvarez Carmen, Doll Ronald, Kurata Hirokazu, Schebye Xiao Min, Parry David, Lees Emma
Molecular Oncology Laboratory, Department of Discovery Research, DNAX Research, Inc., Palo Alto, CA 94304, USA.
Mol Cell Biol. 2004 Jul;24(14):6268-77. doi: 10.1128/MCB.24.14.6268-6277.2004.
To ensure proper progression through a cell cycle, checkpoints have evolved to play a surveillance role in maintaining genomic integrity. In this study, we demonstrate that loss of CDK2 activity activates an intra-S-phase checkpoint. CDK2 inhibition triggers a p53-p21 response via ATM- and ATR-dependent p53 phosphorylation at serine 15. Phosphorylation of other ATM and ATR downstream substrates, such as H2AX, NBS1, CHK1, and CHK2 is also increased. We show that during S phase when CDK2 activity is inhibited, there is an unexpected loading of the minichromosome maintenance complex onto chromatin. In addition, there is an increased number of cells with more than 4N DNA content, detected in the absence of p53, suggesting that rereplication can occur as a result of CDK2 disruption. Our findings identify an important role for CDK2 in the maintenance of genomic stability, acting via an ATM- and ATR-dependent pathway.
为确保细胞周期正常进行,关卡机制逐渐进化以在维持基因组完整性方面发挥监测作用。在本研究中,我们证明CDK2活性丧失会激活S期内关卡。CDK2抑制通过ATM和ATR依赖的丝氨酸15位点p53磷酸化触发p53-p21反应。其他ATM和ATR下游底物,如H2AX、NBS1、CHK1和CHK2的磷酸化也增加。我们表明,在S期当CDK2活性被抑制时,微小染色体维持复合体意外地加载到染色质上。此外,在缺乏p53的情况下检测到DNA含量超过4N的细胞数量增加,这表明CDK2破坏可能导致再复制。我们的研究结果确定了CDK2在通过ATM和ATR依赖途径维持基因组稳定性方面的重要作用。