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直接观察到复制因子与 PCNA 结合时 DNA 接力传递。

Direct visualization of DNA baton pass between replication factors bound to PCNA.

机构信息

Medical Institute of Bioregulation, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka, 812-8582, Japan.

Department of Bioscience and Biotechnology, Graduate School of Bioresource and Bioenvironmental Sciences, Kyushu University, 744 Motooka, Nishi-ku, Fukuoka, 819-0395, Japan.

出版信息

Sci Rep. 2018 Nov 1;8(1):16209. doi: 10.1038/s41598-018-34176-2.

Abstract

In Eukarya and Archaea, the lagging strand synthesis is accomplished mainly by three key factors, DNA polymerase (Pol), flap endonuclease (FEN), and DNA ligase (Lig), in the DNA replication process. These three factors form important complexes with proliferating cell nuclear antigen (PCNA), thereby constructing a platform that enable each protein factor to act successively and smoothly on DNA. The structures of the Pol-PCNA-DNA and Lig-PCNA-DNA complexes alone have been visualized by single particle analysis. However, the FEN-PCNA-DNA complex structure remains unknown. In this report, we for the first time present this tertiary structure determined by single particle analysis. We also successfully visualized the structure of the FEN-Lig-PCNA-DNA complex, corresponding to a putative intermediate state between the removal of the DNA flap by FEN and the sealing of the nicked DNA by Lig. This structural study presents the direct visualization of the handing-over action, which proceeds between different replication factors on a single PCNA clamp bound to DNA. We detected a drastic conversion of the DNA from a bent form to a straight form, in addition to the dynamic motions of replication factors in the switching process.

摘要

在真核生物和古菌中,滞后链的合成主要由三个关键因素完成,即在 DNA 复制过程中,DNA 聚合酶(Pol)、核酸内切酶(FEN)和 DNA 连接酶(Lig)。这三个因素与增殖细胞核抗原(PCNA)形成重要的复合物,从而构建了一个平台,使每个蛋白因子能够在 DNA 上依次顺利地发挥作用。单独的 Pol-PCNA-DNA 和 Lig-PCNA-DNA 复合物的结构已经通过单颗粒分析得以可视化。然而,FEN-PCNA-DNA 复合物的结构仍然未知。在本报告中,我们首次通过单颗粒分析确定了这种三级结构。我们还成功地可视化了 FEN-Lig-PCNA-DNA 复合物的结构,它对应于 FEN 切除 DNA 发夹和 Lig 封闭缺口 DNA 之间的假定中间状态。这项结构研究直接观察了在单个结合于 DNA 的 PCNA 夹上的不同复制因子之间进行的交接作用。我们检测到了 DNA 从弯曲形式到直线形式的剧烈转换,以及在转换过程中复制因子的动态运动。

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