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通过夹板连接法检测和标记小非编码RNA

Detection and labeling of small non-coding RNAs by splinted ligation.

作者信息

Bourgeois Gabrielle, Chardon Florian, Tillault Anne-Sophie, Blaud Magali

机构信息

Laboratoire de Biochimie, CNRS UMR 7654, Ecole Polytechnique, Palaiseau, France.

出版信息

Methods Mol Biol. 2015;1296:65-72. doi: 10.1007/978-1-4939-2547-6_7.

Abstract

Discovery and characterization of microRNAs (miRNAs) and other families of small RNAs lead researchers to study their structures/functions and their expression patterns. The splinted ligation method described here is based on nucleic acid hybridization. It is optimized for the direct labeling and quantitative detection of small RNAs. A specific bridge DNA oligonucleotide is used, which is perfectly complementary to both the target small RNA and a labeled ligation nucleic acid. The target RNA is subsequently labeled by ligation, detected by analysis in denaturing conditions, and quantified by phosphorimaging. The protocol doesn't require any specific material, and the procedure is fast and sensitive.

摘要

微小RNA(miRNA)及其他小RNA家族的发现与特性研究促使研究人员去探究它们的结构/功能及其表达模式。本文所述的夹板连接法基于核酸杂交。它针对小RNA的直接标记和定量检测进行了优化。使用了一种特定的桥DNA寡核苷酸,它与靶标小RNA和标记的连接核酸均完全互补。随后通过连接对靶标RNA进行标记,在变性条件下通过分析进行检测,并通过磷光成像进行定量。该方案不需要任何特殊材料,且操作快速灵敏。

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