Nishitani Hideo, Lygerou Zoi
Department of Molecular Biology, Graduate School of Medical Science, Kyushu University, Fukuoka, 812-8582, Japan.
Genes Cells. 2002 Jun;7(6):523-34. doi: 10.1046/j.1365-2443.2002.00544.x.
To maintain genome integrity in eukaryotes, DNA must be duplicated precisely once before cell division occurs. A process called replication licensing ensures that chromosomes are replicated only once per cell cycle. Its control has been uncovered by the discovery of the CDKs (cyclin dependent kinases) as master regulators of the cell cycle and the initiator proteins of DNA replication, such as the Origin Recognition Complex (ORC), Cdc6/18, Cdt1 and the MCM complex. At the end of mitosis, the MCM complex is loaded on to chromatin with the aid of ORC, Cdc6/18 and Cdt1, and chromatin becomes licensed for replication. CDKs, together with the Cdc7 kinase, trigger the initiation of replication, recruiting the DNA replicating enzymes on sites of replication. The activated MCM complex appears to play a key role in the DNA unwinding step, acting as a replicating helicase and moves along with the replication fork, at the same time bringing the origins to the unlicensed state. The cycling of CDK activity in the cell cycle separates the two states of replication origins, the licensed state in G1-phase and the unlicensed state for the rest of the cell cycle. Only when CDK drops at the completion of mitosis, is the restriction on licensing relieved and a new round of replication is allowed. Such a CDK-regulated licensing control is conserved from yeast to higher eukaryotes, and ensures that DNA replication takes place only once in a cycle. Xenopus laevis and mammalian cells have an additional system to control licensing. Geminin, whose degradation at the end of mitosis is essential for a new round of licensing, has been shown to bind Cdt1 and negatively regulate it, providing a new insight into the regulation of DNA replication in higher eukaryotes.
为维持真核生物基因组的完整性,DNA在细胞分裂发生之前必须精确复制一次。一种称为复制许可的过程可确保染色体在每个细胞周期仅复制一次。细胞周期蛋白依赖性激酶(CDK)作为细胞周期的主要调节因子以及DNA复制起始蛋白(如起始识别复合物(ORC)、Cdc6/18、Cdt1和MCM复合物)的发现,揭示了其控制机制。在有丝分裂末期,MCM复合物借助ORC、Cdc6/18和Cdt1加载到染色质上,染色质即获得复制许可。CDK与Cdc7激酶一起触发复制起始,将DNA复制酶招募到复制位点。活化的MCM复合物似乎在DNA解旋步骤中起关键作用,作为复制解旋酶并随着复制一起移动,同时使起始点进入非许可状态。细胞周期中CDK活性的循环将复制起始点的两种状态区分开来,即G1期的许可状态和细胞周期其余阶段的非许可状态。只有当有丝分裂完成时CDK活性下降,许可限制才会解除,新一轮复制才被允许。这种由CDK调节的许可控制从酵母到高等真核生物都是保守的,并确保DNA在一个周期中仅复制一次。非洲爪蟾和哺乳动物细胞还有一个额外的系统来控制许可。Geminin在有丝分裂末期的降解对于新一轮许可至关重要,已证明它可与Cdt1结合并对其进行负调控,这为高等真核生物中DNA复制的调控提供了新的见解。