School of Medicine, Huaqiao University, Xiamen, Fujian, China.
College of Materials Science and Engineering, Huaqiao University, Xiamen, Fujian, China.
Methods Mol Biol. 2024;2822:143-156. doi: 10.1007/978-1-0716-3918-4_11.
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.
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。