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利用 Psora-seq 进行体内基因组超螺旋作图。

In Vivo Genomic Supercoiling Mapping Using Psora-seq.

机构信息

Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.

出版信息

Methods Mol Biol. 2024;2819:147-156. doi: 10.1007/978-1-0716-3930-6_8.

Abstract

Supercoiling is a fundamental property of DNA that governs all strand opening reactions, including DNA replication, transcription, and homologous recombination. However, traditional genomic supercoiling assays are difficult and lack sensitivity. Building on prior assays using the DNA intercalator psoralen, we developed a supercoil mapping assay that is robust and sensitive to a wide range of supercoiling while requiring only commercially available reagents and common laboratory equipment. This method, psoralen affinity purification with genomic sequencing (Psora-seq), utilizes biotinylated psoralen and streptavidin-conjugated magnetic beads to facilitate efficient pull-down of psoralen-bound DNA, followed by deep sequencing to identify and quantify supercoiling at 1 kb resolution. Psora-seq overcomes two major bottlenecks associated with existing psoralen pull-down assays, inefficient photo-binding of psoralen-bound molecules, and poor recovery of cross-linked DNA.

摘要

超螺旋是 DNA 的基本性质,它控制着所有链打开反应,包括 DNA 复制、转录和同源重组。然而,传统的基因组超螺旋检测方法既困难又缺乏灵敏度。在先前使用 DNA 嵌入剂补骨脂素的检测方法的基础上,我们开发了一种超螺旋作图检测方法,该方法对广泛的超螺旋具有稳健性和敏感性,同时只需要商业上可用的试剂和常见的实验室设备。这种方法,即补骨脂素亲和纯化与基因组测序(Psora-seq),利用生物素化补骨脂素和链霉亲和素修饰的磁珠来促进补骨脂素结合的 DNA 的有效下拉,然后进行深度测序,以确定和定量 1kb 分辨率的超螺旋。Psora-seq 克服了与现有补骨脂素下拉检测方法相关的两个主要瓶颈,即补骨脂素结合分子的光结合效率低和交联 DNA 的回收率差。

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