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实时同源重组:RecA介导的DNA链交换

Homologous recombination in real time: DNA strand exchange by RecA.

作者信息

van der Heijden Thijn, Modesti Mauro, Hage Susanne, Kanaar Roland, Wyman Claire, Dekker Cees

机构信息

Kavli Institute of Nanoscience, Delft University of Technology, Lorentzweg 1, 2628 CJ Delft, The Netherlands.

出版信息

Mol Cell. 2008 May 23;30(4):530-8. doi: 10.1016/j.molcel.2008.03.010.

Abstract

Homologous recombination, the exchange of strands between different DNA molecules, is essential for proper maintenance and accurate duplication of the genome. Using magnetic tweezers, we monitor RecA-driven homologous recombination of individual DNA molecules in real time. We resolve several key aspects of DNA structure during and after strand exchange. Changes in DNA length and twist yield helical parameters for the protein-bound three-stranded structure in conditions in which ATP was not hydrolyzed. When strand exchange was completed under ATP hydrolysis conditions that allow protein dissociation, a "D wrap" structure formed. During homologous recombination, strand invasion at one end and RecA dissociation at the other end occurred at the same rate, and our single-molecule analysis indicated that a region of only about 80 bp is actively involved in the synapsis at any time during the entire reaction involving a long ( approximately 1 kb) region of homology.

摘要

同源重组,即不同DNA分子间链的交换,对于基因组的正常维持和精确复制至关重要。我们使用磁镊实时监测RecA驱动的单个DNA分子的同源重组。我们解析了链交换过程中和之后DNA结构的几个关键方面。在未水解ATP的条件下,DNA长度和扭转的变化产生了与蛋白质结合的三链结构的螺旋参数。当在允许蛋白质解离的ATP水解条件下完成链交换时,形成了一种“D环”结构。在同源重组过程中,一端的链侵入和另一端的RecA解离以相同的速率发生,并且我们的单分子分析表明,在涉及长约1 kb同源区域的整个反应过程中,任何时候只有约80 bp的区域积极参与联会。

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