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使用单分子 DNA 幕技术和电泳迁移率变动分析研究 R 环识别蛋白。

Studying R-Loop Recognizing Proteins Using Single-Molecule DNA Curtain Technique and Electrophoretic Mobility Shift Assay.

机构信息

Department of Biological Sciences, Ulsan National Institute of Science and Technology, Ulsan, Republic of Korea.

Center for Genomic Integrity, Institute for Basic Science, Ulsan, Republic of Korea.

出版信息

Methods Mol Biol. 2022;2528:253-269. doi: 10.1007/978-1-0716-2477-7_16.

Abstract

R-loops are nucleic acid structures containing a DNA-RNA hybrid and the associated non-template single-stranded DNA. R-loops are not only involved in many biological processes but also cause genomic instability when they are abnormally regulated. The R-loop regulation pathway consists of multiple steps associated with diverse proteins. The initial and essential step of the pathway is to recognize R-loops in long DNA of human genome. To elucidate the molecular mechanism underlying R-loop recognition by proteins, we utilize a novel high-throughput single-molecule approach called "DNA curtain" as well as electrophoretic mobility shift assays. Here, we describe the detailed protocols for these techniques that both can be used for studying the R-loop recognition mechanisms.

摘要

R 环是一种含有 DNA-RNA 杂合体和相关非模板单链 DNA 的核酸结构。R 环不仅参与许多生物过程,而且当它们被异常调节时还会导致基因组不稳定。R 环调节途径包含与多种蛋白质相关的多个步骤。该途径的初始和基本步骤是识别人类基因组中长 DNA 中的 R 环。为了阐明蛋白质识别 R 环的分子机制,我们利用一种称为“DNA 幕帘”的新型高通量单分子方法以及电泳迁移率变动分析。在这里,我们描述了这两种技术的详细方案,均可用于研究 R 环识别机制。

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