You Zhiying, Masai Hisao
Genome Dynamics Project, Department of Basic Medical Sciences, Tokyo Metropolitan Institute of Medical Science, Setagaya-ku, Tokyo 156-8506, Japan.
Department of Computational Biology and Medical Sciences, Graduate School of Frontier Sciences, The University of Tokyo, Chiba 277-8561, Japan.
Biology (Basel). 2024 Aug 17;13(8):629. doi: 10.3390/biology13080629.
In this review, we summarize the processes of the assembly of multi-protein replisomes at the origins of replication. Replication licensing, the loading of inactive minichromosome maintenance double hexamers (dhMCM2-7) during the G1 phase, is followed by origin firing triggered by two serine-threonine kinases, Cdc7 (DDK) and CDK, leading to the assembly and activation of Cdc45/MCM2-7/GINS (CMG) helicases at the entry into the S phase and the formation of replisomes for bidirectional DNA synthesis. Biochemical and structural analyses of the recruitment of initiation or firing factors to the dhMCM2-7 for the formation of an active helicase and those of origin melting and DNA unwinding support the steric exclusion unwinding model of the CMG helicase.
在本综述中,我们总结了多蛋白复制体在复制起点处的组装过程。复制许可,即在G1期加载无活性的微型染色体维持双六聚体(dhMCM2-7),随后由两种丝氨酸 - 苏氨酸激酶Cdc7(DDK)和CDK触发复制起点激活,导致在进入S期时Cdc45/MCM2-7/GINS(CMG)解旋酶的组装和激活,并形成用于双向DNA合成的复制体。对起始或激活因子募集到dhMCM2-7以形成活性解旋酶的生化和结构分析,以及对复制起点解链和DNA解旋的分析,支持了CMG解旋酶的空间排斥解旋模型。