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DNA复制中间体的几何结构和拓扑结构新见解。

New Insights into the Geometry and Topology of DNA Replication Intermediates.

作者信息

Martínez Victor, Ruiz-Díaz Edith, Cardozo Delia, Cappo Cristian, Schaerer Christian E, Cebrián Jorge, Krimer Dora B, Fernández-Nestosa María José

机构信息

Bioinformatic Laboratory, Polytechnic School, National University of Asuncion, San Lorenzo 2111, Paraguay.

The Technological Research and Development Nucleus, Polytechnic School, National University of Asuncion, San Lorenzo 2111, Paraguay.

出版信息

Biology (Basel). 2025 Apr 26;14(5):478. doi: 10.3390/biology14050478.

Abstract

The regulation of superhelical stress, mediated by the combined action of topoisomerases and fork rotation, is crucial for DNA replication. The conformational changes during DNA replication are still experimentally challenging, mainly due to the rapid kinetics of the replication process. Here, we present the first molecular dynamics simulations of partially replicated circular DNA molecules, with stalled replication forks at both early and late stages of DNA replication. These simulations allowed us to map the distribution of superhelical stress after deproteinization. We propose a five-component model that determines the linking number difference of replication intermediates. At a thermodynamic equilibrium, the contribution of these five components was correlated to the progress of the replication forks. Additionally, we identified four types of segment collision events in replication intermediates, characterized by their geometric properties, including chirality and topological sign. The distribution of these collision events between the early and late stages of DNA replication provides new insights into the coordinated function of topoisomerases, warranting further discussion.

摘要

由拓扑异构酶和叉旋转的联合作用介导的超螺旋应力调节对于DNA复制至关重要。DNA复制过程中的构象变化在实验上仍然具有挑战性,主要是由于复制过程的快速动力学。在这里,我们展示了部分复制的环状DNA分子的首次分子动力学模拟,在DNA复制的早期和晚期都有停滞的复制叉。这些模拟使我们能够绘制去蛋白化后超螺旋应力的分布。我们提出了一个五组分模型,该模型确定复制中间体的连接数差异。在热力学平衡时,这五个组分的贡献与复制叉的进展相关。此外,我们在复制中间体中识别出四种类型的片段碰撞事件,其特征在于它们的几何性质,包括手性和拓扑符号。这些碰撞事件在DNA复制早期和晚期之间的分布为拓扑异构酶的协同功能提供了新的见解,值得进一步讨论。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/daa8/12109278/3b355b09e16f/biology-14-00478-g001.jpg

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