Clare Hall Laboratories, Cancer Research UK, South Mimms, UK.
Methods. 2012 Jun;57(2):222-6. doi: 10.1016/j.ymeth.2012.06.008. Epub 2012 Jun 23.
Licensing of origins of eukaryotic DNA replication involves the loading of six minichromosome maintenance proteins (Mcm2-7) into pre-replicative complexes (pre-RCs). The assembly of the pre-RC is restricted to G1 phase of the cell cycle, which is crucial to ensure once per cell cycle DNA replication. Mcm2-7 is loaded by the action of the origin recognition complex (ORC), Cdc6 and Cdt1 and requires ATP. In vitro reconstitution of this reaction has shown that Mcm2-7 is loaded onto DNA as a symmetrical head-to-head double hexamer. We describe in detail how pre-RC proteins are purified and used to reconstitute pre-RC formation in vitro. This method is useful for studying the biochemical mechanisms of Mcm2-7 loading as well as subsequent steps in DNA replication.
真核生物 DNA 复制原点的许可涉及将六个微小染色体维持蛋白(Mcm2-7)装入复制前复合物(pre-RC)中。pre-RC 的组装仅限于细胞周期的 G1 期,这对于确保细胞周期中 DNA 复制一次至关重要。Mcm2-7 通过原点识别复合物(ORC)、Cdc6 和 Cdt1 的作用加载,并需要 ATP。体外重建该反应表明,Mcm2-7 作为对称的头对头双六聚体加载到 DNA 上。我们详细描述了如何纯化 pre-RC 蛋白并用于体外重建 pre-RC 形成。该方法可用于研究 Mcm2-7 加载的生化机制以及 DNA 复制的后续步骤。