Department of Plant Sciences, University of Cambridge, Cambridge, UK.
Department of Algal Development and Evolution, Max Planck Institute for Biology Tübingen, Tübingen, Germany.
Methods Mol Biol. 2023;2630:47-66. doi: 10.1007/978-1-0716-2982-6_4.
Small RNAs (sRNAs) are key regulators of transcriptomes and proteomes of organisms through their sequence-specific interaction with complementary RNA targets. sRNAs can be classified according to their origin and mode of action into different classes such as: microRNAs (miRNAs), small interfering RNAs (siRNAs) and PIWI-interacting RNAs (piRNAs). The abundance and specific spatio-temporal expression of many sRNAs, especially miRNAs, is relevant for their biological function. Northern blotting is a widely used technique to study sRNAs because it is quantitative, relatively inexpensive, and readily available for most laboratories. This chapter describes the protocols for radioactive and non-radioactive sRNA Northern blot analysis, which includes RNA extraction, polyacrylamide gel electrophoresis, membrane transfer, hybridisation and detection of sRNA using oligonucleotide probes. The protocol is described to prepare most of the reagents needed in the lab, but also timesaving commercial reagent alternatives are included. Suggestions and nuances obtained from experience are included as Notes.
小 RNA(sRNA)通过与互补 RNA 靶标特异性序列相互作用,成为调控生物转录组和蛋白质组的关键因子。根据起源和作用方式的不同,sRNA 可以分为不同的类别,如 microRNAs(miRNAs)、small interfering RNAs(siRNAs)和 PIWI-interacting RNAs(piRNAs)。许多 sRNA(特别是 miRNAs)的丰度和特定时空表达与其生物学功能相关。Northern 印迹是一种广泛用于研究 sRNA 的技术,因为它具有定量、相对廉价且易于在大多数实验室获得的特点。本章描述了放射性和非放射性 sRNA Northern 印迹分析的方案,包括 RNA 提取、聚丙烯酰胺凝胶电泳、膜转移、杂交以及使用寡核苷酸探针检测 sRNA。该方案描述了制备实验室所需的大部分试剂,但也包括节省时间的商业试剂替代方案。还包括了从经验中获得的建议和细微差别。