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小RNA的定量逆转录聚合酶链反应

qRT-PCR of Small RNAs.

作者信息

Varkonyi-Gasic Erika, Hellens Roger P

机构信息

HortResearch, Mt Albert Research Centre, Auckland, New Zealand.

出版信息

Methods Mol Biol. 2010;631:109-22. doi: 10.1007/978-1-60761-646-7_10.

Abstract

Plant small RNAs are a class of 19- to 25-nucleotide (nt) RNA molecules that are essential for genome stability, development and differentiation, disease, cellular communication, signaling, and adaptive responses to biotic and abiotic stress. Small RNAs comprise two major RNA classes, short interfering RNAs (siRNAs) and microRNAs (miRNAs). Efficient and reliable detection and quantification of small RNA expression has become an essential step in understanding their roles in specific cells and tissues. Here we provide protocols for the detection of miRNAs by stem-loop RT-PCR. This method enables fast and reliable miRNA expression profiling from as little as 20 pg of total RNA extracted from plant tissue and is suitable for high-throughput miRNA expression analysis. In addition, this method can be used to detect other classes of small RNAs, provided the sequence is known and their GC contents are similar to those specific for miRNAs.

摘要

植物小RNA是一类19至25个核苷酸(nt)的RNA分子,对基因组稳定性、发育与分化、疾病、细胞通讯、信号传导以及对生物和非生物胁迫的适应性反应至关重要。小RNA包括两大类RNA,即小干扰RNA(siRNA)和微小RNA(miRNA)。高效且可靠地检测和定量小RNA表达已成为了解它们在特定细胞和组织中作用的关键步骤。在此,我们提供通过茎环RT-PCR检测miRNA的方案。该方法能够从仅20 pg植物组织提取的总RNA中快速且可靠地进行miRNA表达谱分析,适用于高通量miRNA表达分析。此外,只要序列已知且其GC含量与miRNA特有的GC含量相似,该方法还可用于检测其他类别的小RNA。

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