IGMM, CNRS, Université de Montpellier, Montpellier, France.
Université de Lorraine, CNRS, IMoPA, F-54000 Nancy, France.
Methods Mol Biol. 2021;2300:119-131. doi: 10.1007/978-1-0716-1386-3_12.
This chapter describes one of the most reliable quantitative assays to test the silencing of a possible target gene by a specific miRNA using a luciferase reporter gene. The experimental procedure first consists in cloning both the wild-type and mutated forms of the 3'UTR of the miRNA-predicted mRNA target downstream of a firefly luciferase reporter. Next, each construct is co-transfected together with the miRNA into HeLa cells, and the reporter expression is monitored. Changes in luciferase levels will indicate whether or not an miRNA can bind to the UTR and regulate its expression.
本章描述了一种最可靠的定量测定方法,用于使用荧光素酶报告基因检测特定 miRNA 对可能的靶基因的沉默作用。实验程序首先包括将 miRNA 预测的 mRNA 靶基因的 3'UTR 的野生型和突变型克隆到萤火虫荧光素酶报告基因的下游。接下来,将每个构建体与 miRNA 一起共转染到 HeLa 细胞中,并监测报告基因的表达。荧光素酶水平的变化将表明 miRNA 是否可以结合到 UTR 并调节其表达。