Kiyama Takae, Mao Chai-An
Ruiz Department of Ophthalmology and Visual Science, McGovern Medical School, The University of Texas Health Science Center at Houston (UTHealth), Houston, TX, USA.
Methods Mol Biol. 2020;2092:147-158. doi: 10.1007/978-1-0716-0175-4_11.
In situ hybridization (ISH) techniques provide important information regarding gene expression in cells and tissues. Especially, ISH details complex spatial RNA expression in highly heterogeneous tissues, such as developing and mature central nervous systems, where rare genes involved in many fundamental developmental or biological events are expressed. Although several techniques have been developed to detect low levels of RNA expression, there are still problematic issues caused by a low signal-to-noise ratio after signal amplification. RNAscope is a recently developed ISH technique with high sensitivity and low background. RNAscope utilizes a unique probe system (double Z probe) to amplify signal from rare RNAs. Additionally, the double Z probe enables a significant reduction in nonspecific signal amplification. Here we report detailed procedures of the brown-color RNAscope ISH on embryonic and adult mouse retinas.
原位杂交(ISH)技术提供了有关细胞和组织中基因表达的重要信息。特别是,ISH能详细显示高度异质性组织中复杂的空间RNA表达情况,比如发育中和成熟的中枢神经系统,其中涉及许多基本发育或生物学事件的稀有基因会在此处表达。尽管已经开发了多种技术来检测低水平的RNA表达,但信号放大后仍存在信噪比低所导致的问题。RNAscope是一种最近开发的具有高灵敏度和低背景的ISH技术。RNAscope利用独特的探针系统(双Z探针)来放大稀有RNA的信号。此外,双Z探针能够显著减少非特异性信号放大。在此,我们报告在胚胎和成年小鼠视网膜上进行棕色RNAscope原位杂交的详细步骤。