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通过嵌合体PCR(ChimP)检测微小RNA-靶标相互作用

Detection of microRNA-Target Interactions by Chimera PCR (ChimP).

作者信息

Broughton James P, Pasquinelli Amy E

机构信息

Department of Dermatology, Stanford University School of Medicine, Stanford, CA, USA.

Division of Biology, University of California, San Diego, La Jolla, CA, USA.

出版信息

Methods Mol Biol. 2018;1823:153-165. doi: 10.1007/978-1-4939-8624-8_12.

Abstract

MicroRNAs (miRNAs) regulate gene expression by directing Argonaute proteins to target RNAs, which usually results in destabilization and translational inhibition of the target RNA. The prediction of animal miRNA target sites has remained a challenge due to the ability of miRNAs to bind target RNAs through imperfect base pairing. Recently, several labs have established methods to produce biochemical evidence of miRNA-target interactions by generating chimeric reads where the miRNA is ligated to its target RNA. Despite the insights that can be gained from chimera producing methods, the current approaches are inefficient, labor intensive and require computational expertise. Here we describe a method, called Chimera PCR (ChimP), for the validation or testing of specific miRNA-target interactions. This method allows for focused experiments to analyze miRNA targeting in a variety of conditions.

摘要

微小RNA(miRNA)通过引导AGO蛋白作用于靶RNA来调控基因表达,这通常会导致靶RNA的稳定性降低及翻译抑制。由于miRNA能够通过不完全碱基配对与靶RNA结合,因此预测动物miRNA的靶位点仍然是一项挑战。最近,几个实验室已经建立了一些方法,通过生成嵌合 reads(其中miRNA与它的靶RNA连接)来提供miRNA-靶标相互作用的生化证据。尽管嵌合体生成方法能提供一些见解,但目前的方法效率低下、劳动强度大且需要计算专业知识。在这里,我们描述了一种名为嵌合体PCR(ChimP)的方法,用于验证或测试特定的miRNA-靶标相互作用。该方法允许进行针对性实验,以分析各种条件下的miRNA靶向作用。

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