Institute for Systems Genetics, NYU Grossman School of Medicine, New York, NY, USA.
Department of Molecular Genetics and Microbiology, University of Florida, Gainesville, FL, USA.
Methods Mol Biol. 2024;2784:163-176. doi: 10.1007/978-1-0716-3766-1_11.
RNA fluorescence in situ hybridization (FISH) is a powerful method to determine the abundance and localization of mRNA molecules in cells. While modern RNA FISH techniques allow quantification at single molecule resolution, most methods are optimized for mammalian cell culture and are not easily applied to in vivo tissue settings. Single-molecule RNA detection in skeletal muscle cells has been particularly challenging due to the thickness and high autofluorescence of adult muscle tissue and a lack of in vitro models for mature muscle cells (myofibers). Here, we present a method for isolation of adult myofibers from mouse skeletal muscle and detection of single mRNA molecules and proteins using multiplexed RNA FISH and immunofluorescence.
RNA 荧光原位杂交(FISH)是一种确定细胞中 mRNA 分子丰度和定位的强大方法。虽然现代 RNA FISH 技术允许以单分子分辨率进行定量,但大多数方法都针对哺乳动物细胞培养进行了优化,并且不容易应用于体内组织环境。由于成年肌肉组织的厚度和高自发荧光以及缺乏成熟肌肉细胞(肌纤维)的体外模型,骨骼肌细胞中单分子 RNA 的检测一直特别具有挑战性。在这里,我们提出了一种从小鼠骨骼肌中分离成年肌纤维并使用多重 RNA FISH 和免疫荧光检测单个 mRNA 分子和蛋白质的方法。