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A conserved Mcm4 motif is required for Mcm2-7 double-hexamer formation and origin DNA unwinding

机译:Mcm2-7双六聚体形成和起始DNA展开需要保守的Mcm4基序

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摘要

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.
机译:真核生物复制起点的许可需要DNA加载两个副本的Mcm2-7复制解旋酶以形成头对头双六聚体,以确保活化的解旋酶双向离开该起点。为了了解这种双六聚体的形成和重要性,我们鉴定了一个保守且必不可少的Mcm4基序中的突变,该突变允许加载两个Mcm2-7复合物,但对双六聚体的形成有缺陷。单分子研究表明,突变体Mcm2-7形成了最初的六聚体-六聚体相互作用。然而,所得的络合物是不稳定的。对野生型和突变型Mcm2-7的动力学分析揭示了在第二次Mcm2-7缔合后双六聚体形成的有限时间窗口,表明该过程得到了促进。展开大量来源的DNA时需要双六聚体的形成,但最初的DNA融化或解旋酶激活蛋白(Cdc45,GINS,Mcm10)的募集则不需要。我们的发现阐明了原产地许可的动态机制,并确定了最初的DNA融化和大量解开之间的过渡是需要双六聚体形成的第一个起始事件。

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