Bayer Livia V, Batish Mona, Formel Stephen K, Bratu Diana P
Department of Biological Sciences, Hunter College of the City University of New York, 695 Park Avenue, New York, NY, 10021, USA.
Methods Mol Biol. 2015;1328:125-36. doi: 10.1007/978-1-4939-2851-4_9.
Detection of nucleic acids in whole tissues has become key in our understanding of gene expression during development. In situ hybridization (ISH) has been an invaluable technique in the making of numerous discoveries. Most recently, the technical advance of using short, fluorescently labeled probes has allowed for the detection of single-mRNA molecules. Thus, quantification of RNA levels in single cells or even within subcellular regions is now possible without RNA isolation. In combination with the immunofluorescence (IF) technique, visualization of nucleic acids and associating proteins is achieved with higher resolution than ever before using light microscopy. Here we describe the steps implemented to achieve the visualization of individual messenger RNAs (mRNA) using single-molecule FISH (smFISH) probes, as well as detection of mRNA/protein (mRNP) complexes via smFISH in combination with IF.
全组织中核酸的检测已成为我们理解发育过程中基因表达的关键。原位杂交(ISH)在众多发现中一直是一项极具价值的技术。最近,使用短的、荧光标记探针的技术进步使得单个mRNA分子的检测成为可能。因此,现在无需分离RNA就可以对单细胞甚至亚细胞区域内的RNA水平进行定量。与免疫荧光(IF)技术相结合,利用光学显微镜可以以前所未有的高分辨率实现核酸和相关蛋白质的可视化。在这里,我们描述了使用单分子FISH(smFISH)探针实现单个信使RNA(mRNA)可视化的步骤,以及通过smFISH结合IF检测mRNA/蛋白质(mRNP)复合物的方法。