The MRC Protein Phosphorylation and Ubiquitylation Unit, School of Life Sciences, University of Dundee, Dundee, UK.
MRC Laboratory of Molecular Biology, Francis Crick Avenue, Cambridge, UK.
Science. 2023 Sep 22;381(6664):eadi4932. doi: 10.1126/science.adi4932.
Assembly of the CMG (CDC-45-MCM-2-7-GINS) helicase is the key regulated step during eukaryotic DNA replication initiation. Until now, it was unclear whether metazoa require additional factors that are not present in yeast. In this work, we show that DNSN-1, the ortholog of human DONSON, functions during helicase assembly in a complex with MUS-101/TOPBP1. DNSN-1 is required to recruit the GINS complex to chromatin, and a cryo-electron microscopy structure indicates that DNSN-1 positions GINS on the MCM-2-7 helicase motor (comprising the six MCM-2 to MCM-7 proteins), by direct binding of DNSN-1 to GINS and MCM-3, using interfaces that we show are important for initiation and essential for viability. These findings identify DNSN-1 as a missing link in our understanding of DNA replication initiation, suggesting that initiation defects underlie the human disease syndrome that results from DONSON mutations.
CMG(CDC-45-MCM-2-7-GINS)解旋酶的组装是真核 DNA 复制起始的关键调节步骤。到目前为止,尚不清楚后生动物是否需要在酵母中不存在的其他因子。在这项工作中,我们表明,人类 DONSON 的直系同源物 DNSN-1 在与 MUS-101/TOPBP1 形成的复合物中,在解旋酶组装过程中发挥作用。DNSN-1 需要招募 GINS 复合物到染色质上,并且低温电子显微镜结构表明,DNSN-1 通过直接结合 DNSN-1 到 GINS 和 MCM-3,使用我们表明对于起始很重要且对生存力至关重要的界面,将 GINS 定位在 MCM-2-7 解旋酶马达(包含六个 MCM-2 到 MCM-7 蛋白)上。这些发现确定了 DNSN-1 是我们理解 DNA 复制起始的缺失环节,表明 DONSON 突变导致的人类疾病综合征的起始缺陷。