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Nature communications. 2024 Nov 2;15(1):9485. doi: 10.1038/s41467-024-53187-4 Q114.72024

Molecular mechanism of parental H3/H4 recycling at a replication fork

父母本H3/H4在复制叉上的分子回收机制 翻译改进

Fritz Nagae  1, Yasuto Murayama  2  3, Tsuyoshi Terakawa  4

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作者单位

  • 1 Department of Biophysics, Graduate School of Science, Kyoto University, Kyoto, Japan.
  • 2 Department of Chromosome Science, National Institute of Genetics, Shizuoka, Japan.
  • 3 Department of Genetics, Graduate University for Advanced Studies (SOKENDAI), Shizuoka, Japan.
  • 4 Department of Biophysics, Graduate School of Science, Kyoto University, Kyoto, Japan. terakawa@biophys.kyoto-u.ac.jp.
  • DOI: 10.1038/s41467-024-53187-4 PMID: 39488545

    摘要 中英对照阅读

    In chromatin replication, faithful recycling of histones from parental DNA to replicated strands is essential for maintaining epigenetic information across generations. A previous experiment has revealed that disrupting interactions between the N-terminal tail of Mcm2, a subunit in DNA replication machinery, and a histone H3/H4 tetramer perturb the recycling. However, the molecular pathways and the factors that regulate the ratio recycled to each strand and the destination location are yet to be revealed. Here, we performed molecular dynamics simulations of yeast DNA replication machinery, an H3/H4 tetramer, and replicated DNA strands. The simulations demonstrated that histones are recycled via Cdc45-mediated and unmediated pathways without histone chaperones, as our in vitro biochemical assays supported. Also, RPA binding regulated the ratio recycled to each strand, whereas DNA bending by Pol ε modulated the destination location. Together, the simulations provided testable hypotheses, which are vital for elucidating the molecular mechanisms of histone recycling.

    Keywords:molecular mechanism; parental h3/h4; recycling; replication fork

    在染色质复制过程中,从亲代DNA到复制品链的组蛋白忠实回收对于跨世代保持表观遗传信息至关重要。之前的一项实验揭示了破坏Mcm2(DNA复制机器的一个亚基)N端尾部与H3/H4四聚体之间的相互作用会干扰这一过程。然而,调控每条链回收比例和目的地位置的分子途径及因子尚未被揭示。在这里,我们对酵母DNA复制机器、H3/H4四聚体和复制品链进行了分子动力学模拟。这些模拟表明组蛋白通过Cdc45介导和非中介的途径进行回收,并且没有组蛋白伴侣参与,这一点也得到了我们在体外生化实验的支持。此外,RPA结合调控了每条链的回收比例,而Pol ε对DNA的弯曲则调节了目的地位置。综上所述,这些模拟提供了可测试的假说,这对于阐明组蛋白回收的分子机制至关重要。

    © 2024. The Author(s).

    关键词:分子机制; 父母h3/h4; 循环; 复制叉

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    期刊名:Nature communications

    缩写:NAT COMMUN

    ISSN:2041-1723

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    IF/分区:14.7/Q1

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