Saxena Sandeep, Dutta Anindya
Department of Biochemistry and Molecular Genetics, University of Virginia, Charlottesville, VA 22908, USA.
Mutat Res. 2005 Jan 6;569(1-2):111-21. doi: 10.1016/j.mrfmmm.2004.05.026.
A cell limits its DNA replication activity to once per cell division cycle to maintain its genomic integrity. Studies in a variety of organisms are elucidating how these controls are exercised. Key amongst these is the regulation of replication initiator proteins such as Cdt1. Cdt1 is present in cells in G1 phase where it is required for initiation of replication. Once origins have fired, Cdt1 is either exported out of the nucleus or degraded, thereby preventing another round of replication. Higher eukaryotes have evolved another redundant mechanism, an inhibitor called geminin, to restrain Cdt1 activity. Studies in multiple organisms have shown that unregulated Cdt1 activity stimulates overreplication of the genome. Interestingly, the same seems to be true when geminin is depleted. The imbalance in the activities of these proteins causes the activation of key checkpoint proteins, the ATM/ATR kinases and the tumor suppressor, p53. This review proposes that a balance between Cdt1 and geminin is important for maintaining genomic stability.
细胞将其DNA复制活动限制在每个细胞分裂周期一次,以维持其基因组完整性。对多种生物体的研究正在阐明这些控制是如何实施的。其中关键的是对复制起始蛋白如Cdt1的调控。Cdt1存在于G1期的细胞中,在那里它是复制起始所必需的。一旦复制起点启动,Cdt1要么被输出到细胞核外,要么被降解,从而防止新一轮的复制。高等真核生物进化出了另一种冗余机制,一种名为geminin的抑制剂,以抑制Cdt1的活性。对多种生物体的研究表明,不受调控的Cdt1活性会刺激基因组的过度复制。有趣的是,当geminin缺失时似乎也是如此。这些蛋白质活性的失衡会导致关键检查点蛋白、ATM/ATR激酶和肿瘤抑制因子p53的激活。本综述提出,Cdt1和geminin之间的平衡对于维持基因组稳定性很重要。