Zöllner Hannah, Hahn Stephan A, Maghnouj Abdelouahid
Labor für Molekulare Gastroenterologische Onkologie (MGO), Zentrum für Klinische Forschung (ZKF), Ruhr Universität Bochum, Bochum, Germany.
Methods Mol Biol. 2014;1095:121-34. doi: 10.1007/978-1-62703-703-7_10.
Quantification of microRNAs (miRNAs) in cells or primary tissues is one of the most important steps in elucidating their biological functions. However, miRNAs are challenging molecules for PCR amplification due to the stable hairpin of the precursor form and the small size of the mature miRNA, which is roughly the same length as the primers used in standard PCR. To date, different assays were introduced for the specific and sensitive quantification of the mature form of miRNAs. In this chapter we describe the extraction of RNA from microdissected tissue and the quantification of miRNAs using two different methods (stem-loop qRT-PCR and polyT adaptor qRT-PCR).
对细胞或原代组织中的微小RNA(miRNA)进行定量分析是阐明其生物学功能的最重要步骤之一。然而,由于前体形式的稳定发夹结构以及成熟miRNA的小尺寸,miRNA对于PCR扩增而言是具有挑战性的分子,成熟miRNA的长度与标准PCR中使用的引物大致相同。迄今为止,已引入了不同的检测方法用于对成熟形式的miRNA进行特异性和灵敏的定量分析。在本章中,我们描述了从显微切割组织中提取RNA以及使用两种不同方法(茎环定量逆转录PCR和聚T接头定量逆转录PCR)对miRNA进行定量分析的方法。