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槽式印迹杂交检测 R 环。

Slot Blot Assay for Detection of R Loops.

机构信息

Department of BioEngineering and BioMedical Sciences, Biological Systems and Engineering Division, Lawrence Berkeley National Laboratory, Berkeley, CA, USA.

出版信息

Methods Mol Biol. 2023;2701:149-156. doi: 10.1007/978-1-0716-3373-1_9.

Abstract

R loops (DNA-RNA hybrid) are three-stranded nucleic acid structures that comprise of template DNA strand hybridized with the nascent RNA leaving the displaced non-template strand. Although a programmed R loop formation can serve as powerful regulators of gene expression, these structures can also turn into major sources of genomic instability and contribute to the development of diseases. Therefore, understanding how cells prevent the deleterious consequences of R loops yet allow R loop formation to participate in various physiological processes will help to understand how their homeostasis is maintained. Detection and quantitative measurements of R loops are critical that largely relied on S9.6 antibody. Immunofluorescence methods are frequently used to localize and quantify R loops in the cell but they require specialized tools for analysis and relatively expensive; therefore, they are not always useful for initial assessments of R loop accumulation. Here, we describe an improved slot blot protocol to detect and estimate R loops and show its sensitivity and specificity using the S9.6 antibody. Since specific factors protecting cells from harmful R loop accumulation are expanding, this protocol can be used to determine R loop accumulation in research and clinical settings.

摘要

R 环(DNA-RNA 杂交)是由模板 DNA 链与新生 RNA 杂交形成的三链核酸结构,留下了取代的非模板链。虽然有计划的 R 环形成可以作为基因表达的强大调节剂,但这些结构也可能成为基因组不稳定性的主要来源,并导致疾病的发展。因此,了解细胞如何防止 R 环的有害后果,同时允许 R 环形成参与各种生理过程,将有助于了解它们的动态平衡是如何维持的。R 环的检测和定量测量非常关键,这在很大程度上依赖于 S9.6 抗体。免疫荧光法常用于在细胞中定位和定量 R 环,但它们需要专门的分析工具,且相对昂贵;因此,它们并不总是对 R 环积累的初步评估有用。在这里,我们描述了一种改进的狭缝印迹杂交(slot blot)协议来检测和估计 R 环,并使用 S9.6 抗体显示其灵敏度和特异性。由于保护细胞免受有害 R 环积累的特定因素正在不断增加,因此该协议可用于研究和临床环境中的 R 环积累的检测。

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