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通过二维(2D)天然-天然琼脂糖凝胶电泳分析原核细胞中的分支DNA复制和重组中间体。

Analysis of branched DNA replication and recombination intermediates from prokaryotic cells by two-dimensional (2D) native-native agarose gel electrophoresis.

作者信息

Robinson Nicholas P

机构信息

Department of Biochemistry, University of Cambridge, Cambridge, UK.

出版信息

Methods Mol Biol. 2013;1054:45-61. doi: 10.1007/978-1-62703-565-1_3.

Abstract

Branched DNA molecules are generated by the essential processes of replication and recombination. Owing to their distinctive extended shapes, these intermediates migrate differently from linear double-stranded DNA under certain electrophoretic conditions. However, these branched species exist in the cell at much low abundance than the bulk linear DNA. Consequently, branched molecules cannot be visualized by conventional electrophoresis and ethidium bromide staining. Two-dimensional native-native agarose electrophoresis has therefore been developed as a method to facilitate the separation and visualization of branched replication and recombination intermediates. A wide variety of studies have employed this technique to examine branched molecules in eukaryotic, archaeal, and bacterial cells, providing valuable insights into how DNA is duplicated and repaired in all three domains of life.

摘要

分支DNA分子是通过复制和重组的基本过程产生的。由于其独特的伸展形状,在某些电泳条件下,这些中间体的迁移方式与线性双链DNA不同。然而,这些分支物种在细胞中的丰度比大量的线性DNA低得多。因此,分支分子无法通过传统的电泳和溴化乙锭染色来观察。二维天然-天然琼脂糖电泳因此被开发为一种便于分离和观察分支复制和重组中间体的方法。各种各样的研究都采用了这种技术来检测真核细胞、古细菌和细菌细胞中的分支分子,为生命的三个领域中DNA如何复制和修复提供了有价值的见解。

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