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真核生物解旋的机制是双链 DNA 解旋酶的剪切过程。

Mechanism of eukaryotic origin unwinding is a dual helicase DNA shearing process.

机构信息

The Rockefeller University, New York City, NY 10065.

HHMI, New York City, NY 10065.

出版信息

Proc Natl Acad Sci U S A. 2023 Dec 26;120(52):e2316466120. doi: 10.1073/pnas.2316466120. Epub 2023 Dec 18.

DOI:10.1073/pnas.2316466120
PMID:38109526
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10756200/
Abstract

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.

摘要

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。

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Nucleus. 2023 Dec;14(1):2229642. doi: 10.1080/19491034.2023.2229642.
2
AtMCM10 promotes DNA replication-coupled nucleosome assembly in Arabidopsis.AtMCM10 促进拟南芥中 DNA 复制偶联核小体组装。
J Integr Plant Biol. 2023 Jan;65(1):203-222. doi: 10.1111/jipb.13438. Epub 2023 Jan 13.
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SV40 T-antigen uses a DNA shearing mechanism to initiate origin unwinding.SV40 T 抗原利用 DNA 剪切机制启动起始解旋。
四十年的真核生物 DNA 复制:从酵母遗传学到复制体的高分辨率冷冻电镜结构。
Proc Natl Acad Sci U S A. 2024 Oct 15;121(42):e2415231121. doi: 10.1073/pnas.2415231121. Epub 2024 Oct 4.
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S-CDK-regulated bipartite interaction of Mcm10 with MCM is essential for DNA replication.S-CDK 调控的 Mcm10 与 MCM 的二元相互作用对 DNA 复制至关重要。
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Assembly, Activation, and Helicase Actions of MCM2-7: Transition from Inactive MCM2-7 Double Hexamers to Active Replication Forks.MCM2-7的组装、激活及解旋酶作用:从无活性的MCM2-7双六聚体到活性复制叉的转变
Biology (Basel). 2024 Aug 17;13(8):629. doi: 10.3390/biology13080629.
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Unwinding of a eukaryotic origin of replication visualized by cryo-EM.冷冻电镜直观呈现真核复制起始点的解旋过程。
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7
Starting DNA Synthesis: Initiation Processes during the Replication of Chromosomal DNA in Humans.起始 DNA 合成:人类染色体 DNA 复制过程中的起始机制。
Genes (Basel). 2024 Mar 14;15(3):360. doi: 10.3390/genes15030360.
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The Initiation of Eukaryotic DNA Replication.真核生物 DNA 复制的启动。
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