Suppr超能文献

霍利迪连接体分支迁移与解离分析

Holliday junction branch migration and resolution assays.

作者信息

Constantinou Angelos, West Stephen C

机构信息

Institute of Biochemistry, University of Lausanne, Epalinges, Switzerland.

出版信息

Methods Mol Biol. 2004;262:239-53. doi: 10.1385/1-59259-761-0:239.

Abstract

Holliday junctions are central intermediates in the process of genetic recombination; they form as a consequence of a reciprocal exchange of strands between paired DNA molecules. Enzymes that specifically recognize and process these junctions are necessary for the formation of recombinant products. In the methods described here, we detail the in vitro construction of two types of Holliday junction: (1) a small synthetic junction formed by the annealing of partially complementary oligonucleotides; and (2) a true recombination intermediate structure formed by RecA protein-mediated strand exchange. The use of these substrates in assays designed to detect Holliday junction branch migration and resolution activities is described.

摘要

霍利迪连接体是基因重组过程中的核心中间体;它们是配对DNA分子之间链的相互交换的结果而形成的。特异性识别和处理这些连接体的酶对于重组产物的形成是必需的。在此处描述的方法中,我们详细说明了两种类型的霍利迪连接体的体外构建:(1)由部分互补寡核苷酸退火形成的小的合成连接体;(2)由RecA蛋白介导的链交换形成的真正的重组中间体结构。还描述了在旨在检测霍利迪连接体分支迁移和拆分活性的分析中使用这些底物的情况。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验