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基于邻近连接的显色原位杂交检测法对单个 RNA 分子的可视化。

Visualization of Individual RNA Molecules by Proximity Ligation-Based Chromogenic In Situ Hybridization Assay.

机构信息

School of Medicine, Huaqiao University, Xiamen, Fujian, China.

College of Materials Science and Engineering, Huaqiao University, Xiamen, Fujian, China.

出版信息

Methods Mol Biol. 2024;2822:143-156. doi: 10.1007/978-1-0716-3918-4_11.

Abstract

RNA in situ hybridization reveals the abundance and location of gene expression in cells or tissues, providing a technical basis for the clinical diagnosis of diseases. In this chapter, we show a "V" shape probe-mediated single-molecule chromogenic in situ hybridization (vsmCISH) technique for bright-field visualization of individual RNA molecules. In our method, several pairs of target hybridization probes are hybridized to RNA molecules and each probe pair forms a "V" shape overhang. The overhang oligonucleotides then mediated the proximity ligation to form DNA circles, followed by rolling circle amplification for signal enhancement and enzyme-catalyzed chromogenic reaction-based readout. The colorimetric assay avoids problems such as photobleaching and autofluorescence of current fluorescent in situ hybridization-based single-molecule RNA detection techniques. Furthermore, the relatively straightforward protocol makes the method useful for biological research and clinical diagnosis applications.

摘要

RNA 原位杂交揭示了细胞或组织中基因表达的丰度和位置,为疾病的临床诊断提供了技术基础。在本章中,我们展示了一种“V”形探针介导的单分子显色原位杂交(vsmCISH)技术,用于单个 RNA 分子的明场可视化。在我们的方法中,几对靶杂交探针与 RNA 分子杂交,每个探针对在 RNA 分子上形成“V”形突出。然后,突出的寡核苷酸介导邻近连接形成 DNA 环,接着进行滚环扩增以增强信号,并进行酶促显色反应的读出。比色测定避免了当前基于荧光原位杂交的单分子 RNA 检测技术中存在的光漂白和自发荧光等问题。此外,相对简单的方案使得该方法可用于生物学研究和临床诊断应用。

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