Department of Biology, Howard Hughes Medical Institute, Massachusetts Institute of Technology, Cambridge, United States.
Microbiology Graduate Program, Massachusetts Institute of Technology, Cambridge, United States.
Elife. 2019 Aug 6;8:e45538. doi: 10.7554/eLife.45538.
Licensing of eukaryotic origins of replication requires DNA loading of two copies of the Mcm2-7 replicative helicase to form a head-to-head double-hexamer, ensuring activated helicases depart the origin bidirectionally. To understand the formation and importance of this double-hexamer, we identified mutations in a conserved and essential Mcm4 motif that permit loading of two Mcm2-7 complexes but are defective for double-hexamer formation. Single-molecule studies show mutant Mcm2-7 forms initial hexamer-hexamer interactions; however, the resulting complex is unstable. Kinetic analyses of wild-type and mutant Mcm2-7 reveal a limited time window for double-hexamer formation following second Mcm2-7 association, suggesting that this process is facilitated. Double-hexamer formation is required for extensive origin DNA unwinding but not initial DNA melting or recruitment of helicase-activation proteins (Cdc45, GINS, Mcm10). Our findings elucidate dynamic mechanisms of origin licensing, and identify the transition between initial DNA melting and extensive unwinding as the first initiation event requiring double-hexamer formation.
真核生物复制起点的许可需要将两个 Mcm2-7 复制解旋酶的拷贝加载到 DNA 上,以形成头对头的双六聚体,从而确保激活的解旋酶能够双向离开起始点。为了了解这种双六聚体的形成和重要性,我们鉴定了 Mcm4 基序中的保守和必需突变,这些突变允许加载两个 Mcm2-7 复合物,但不能形成双六聚体。单分子研究表明,突变的 Mcm2-7 形成初始的六聚体-六聚体相互作用;然而,得到的复合物不稳定。对野生型和突变型 Mcm2-7 的动力学分析表明,在第二个 Mcm2-7 结合后,双六聚体形成的时间窗口有限,这表明这个过程是被促进的。双六聚体的形成对于广泛的起始 DNA 解旋是必需的,但不是初始 DNA 熔化或解旋酶激活蛋白(Cdc45、GINS、Mcm10)的募集所必需的。我们的研究结果阐明了起始许可的动态机制,并确定了从初始 DNA 熔化到广泛解旋的转变是需要双六聚体形成的第一个起始事件。