The Rockefeller University, New York City, NY 10065.
HHMI, New York City, NY 10065.
Proc Natl Acad Sci U S A. 2023 Dec 26;120(52):e2316466120. doi: 10.1073/pnas.2316466120. Epub 2023 Dec 18.
DNA replication in all cells begins with the melting of base pairs at the duplex origin to allow access to single-stranded DNA templates which are replicated by DNA polymerases. In bacteria, origin DNA is presumed to be melted by accessory proteins that allow loading of two ring-shaped replicative helicases around single-strand DNA (ssDNA) for bidirectional unwinding and DNA replication. In eukaryotes, by contrast, two replicative CMG (Cdc45-Mcm2-7-GINS) helicases are initially loaded head to head around origin double-strand DNA (dsDNA), and there does not appear to be a separate origin unwinding factor. This led us to investigate whether head-to-head CMGs use their adenosine triphosphate (ATP)-driven motors to initiate duplex DNA unwinding at the origin. Here, we show that CMG tracks on one strand of the duplex while surrounding it, and this feature allows two head-to-head CMGs to unwind dsDNA by using their respective motors to pull on opposite strands of the duplex. We further show that while CMG is capable of limited duplex unwinding on its own, the extent of unwinding is greatly and rapidly stimulated by addition of the multifunctional CMG-binding protein Mcm10 that is critical for productive initiation of DNA replication in vivo. On the basis of these findings, we propose that Mcm10 is a processivity or positioning factor that helps translate the work performed by the dual CMG motors at the origin into productive unwinding that facilitates bidirectional DNA replication.
所有细胞中的 DNA 复制都是从双链起始处的碱基对解链开始,从而暴露出单链 DNA 模板,随后由 DNA 聚合酶对其进行复制。在细菌中,假定辅助蛋白可使起始 DNA 解链,以便将两个环形复制解旋酶加载到单链 DNA(ssDNA)周围,从而进行双向解旋和 DNA 复制。相比之下,在真核生物中,两个复制 CMG(Cdc45-Mcm2-7-GINS)解旋酶最初是头对头加载到起始双链 DNA(dsDNA)周围的,似乎没有单独的起始解旋因子。这促使我们研究头对头的 CMG 是否利用其三磷酸腺苷(ATP)驱动的马达在起始处启动双链 DNA 的解旋。在这里,我们表明 CMG 在环绕双链的同时在双链的一条链上追踪,这一特征允许两个头对头的 CMG 通过各自的马达拉动双链的相反链来解开 dsDNA。我们进一步表明,虽然 CMG 本身能够进行有限的双链解旋,但加入对体内 DNA 复制起始至关重要的多功能 CMG 结合蛋白 Mcm10 会大大且快速地刺激解旋程度。基于这些发现,我们提出 Mcm10 是一个延伸因子或定位因子,有助于将双 CMG 马达在起始处执行的工作转化为促进双向 DNA 复制的有效解旋。