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用于检测植物微小RNA的茎环定量逆转录聚合酶链反应

Stem-Loop qRT-PCR for the Detection of Plant microRNAs.

作者信息

Varkonyi-Gasic Erika

机构信息

The New Zealand Institute for Plant & Food Research Limited (Plant & Food Research) Mt Albert, Private Bag 92169, Auckland, 1142, New Zealand.

出版信息

Methods Mol Biol. 2017;1456:163-175. doi: 10.1007/978-1-4899-7708-3_13.

Abstract

Plant microRNAs (miRNAs) play important roles in the posttranscriptional regulation of protein-coding genes, and they are essential for a normal development and survival. Mature miRNAs are cleaved from larger precursor RNAs and are typically 21-22 nt long.The small size, the lack of a common feature like a poly(A) tail, 3' end-modifications, and presence of a precursor-all these factors affect the detection and hinder the quantification of miRNAs. The stem-loop qRT-PCR method described here is designed to detect and quantify mature miRNAs in a fast, specific, accurate, and reliable manner. Firstly, a miRNA-specific stem-loop RT primer is hybridized to miRNA and then reverse transcribed. Next, the RT product is amplified and monitored in real time using a miRNA-specific forward primer and a universal reverse primer. This method enables miRNA expression profiling from as little as 10 pg of total RNA, and it is suitable for a relatively high-throughput analysis of miRNA expression.

摘要

植物微小RNA(miRNA)在蛋白质编码基因的转录后调控中发挥着重要作用,对正常发育和生存至关重要。成熟的miRNA从较大的前体RNA中切割而来,通常长度为21-22个核苷酸。其体积小、缺乏诸如多聚腺苷酸尾、3'端修饰等共同特征以及存在前体等所有这些因素都会影响miRNA的检测并阻碍其定量。本文所述的茎环定量逆转录聚合酶链反应(qRT-PCR)方法旨在以快速、特异、准确和可靠的方式检测和定量成熟的miRNA。首先,将miRNA特异性茎环逆转录引物与miRNA杂交,然后进行逆转录。接下来,使用miRNA特异性正向引物和通用反向引物对逆转录产物进行扩增并实时监测。该方法能够从低至10 pg的总RNA中进行miRNA表达谱分析,适用于miRNA表达的相对高通量分析。

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