Ma C J, Steinfeld J B, Greene E C
Columbia University, New York, NY, United States.
Columbia University, New York, NY, United States.
Methods Enzymol. 2017;582:193-219. doi: 10.1016/bs.mie.2016.08.005. Epub 2016 Oct 22.
Homologous recombination is an important pathway involved in the repair of double-stranded DNA breaks. Genetic studies form the foundation of our knowledge on homologous recombination. Significant progress has also been made toward understanding the biochemical and biophysical properties of the proteins, complexes, and reaction intermediates involved in this essential DNA repair pathway. However, heterogeneous or transient recombination intermediates remain extremely difficult to assess through traditional ensemble methods, leaving an incomplete mechanistic picture of many steps that take place during homologous recombination. To help overcome some of these limitations, we have established DNA curtain methodologies as an experimental platform for studying homologous DNA recombination in real-time at the single-molecule level. Here, we present a detailed overview describing the preparation and use of single-stranded DNA curtains in applications related to the study of homologous DNA recombination with emphasis on recent work related to the study of the eukaryotic recombinase Rad51.
同源重组是参与双链DNA断裂修复的重要途径。遗传学研究构成了我们对同源重组认识的基础。在理解参与这一基本DNA修复途径的蛋白质、复合物和反应中间体的生化及生物物理特性方面也取得了重大进展。然而,通过传统的整体方法评估异质或瞬时重组中间体仍然极其困难,这使得同源重组过程中许多步骤的机制图景不完整。为了帮助克服其中一些限制,我们建立了DNA帘幕方法,作为在单分子水平实时研究同源DNA重组的实验平台。在此,我们提供了一份详细概述,描述了单链DNA帘幕在与同源DNA重组研究相关应用中的制备和使用,重点介绍了与真核重组酶Rad51研究相关的近期工作。