Greehey Children's Cancer Research Institute, UT Health San Antonio, San Antonio, Texas.
Altos Labs, Redwood City, California.
Curr Protoc. 2024 Apr;4(4):e1037. doi: 10.1002/cpz1.1037.
R-loops are nucleic acid structures composed of a DNA:RNA hybrid with a displaced non-template single-stranded DNA. Current approaches to identify and map R-loop formation across the genome employ either an antibody targeted against R-loops (S9.6) or a catalytically inactivated form of RNase H1 (dRNH1), a nuclease that can bind and resolve DNA:RNA hybrids via RNA exonuclease activity. This overview article outlines several ways to map R-loops using either methodology, explaining the differences and similarities among the approaches. Bioinformatic analysis of R-loops involves several layers of quality control and processing before visualizing the data. This article provides resources and tools that can be used to accurately process R-loop mapping data and explains the advantages and disadvantages of the resources as compared to one another. © 2024 Wiley Periodicals LLC.
R 环是由 DNA:RNA 杂合体和位移的非模板单链 DNA 组成的核酸结构。目前,识别和绘制基因组中 R 环形成的方法要么使用针对 R 环的抗体(S9.6),要么使用 RNase H1 的无催化活性形式(dRNH1),后者是一种可以通过 RNA 外切核酸酶活性结合和解开 DNA:RNA 杂合体的核酸酶。本文概述了使用这两种方法中的任何一种来绘制 R 环的几种方法,解释了这些方法之间的差异和相似之处。R 环的生物信息学分析在可视化数据之前涉及几个质量控制和处理层。本文提供了可用于准确处理 R 环作图数据的资源和工具,并解释了与彼此相比这些资源的优缺点。© 2024 Wiley Periodicals LLC。