Identifying Targets of Human microRNAs with the LightSwitch Luciferase Assay System using 3′UTR-reporter Constructs and a microRNA Mimic in Adherent Cells

被引:14
作者
Aldred, Shelley Force [1 ]
Collins, Patrick [1 ]
Trinklein, Nathan [1 ]
机构
[1] SwitchGear Genom, Menlo Pk, CA 94025 USA
来源
JOVE-JOURNAL OF VISUALIZED EXPERIMENTS | 2011年 / 55期
关键词
Genetics; Issue; 55; MicroRNA; miRNA; mimic; Clone; 3 ' UTR; Assay; vector; LightSwitch; luciferase; co-transfection; 3 ' UTR REPORTER; mirna target; microrna target; reporter; GoClone; Reporter construct; MESSENGER-RNAS; CANCER;
D O I
10.3791/3343
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
MicroRNAs (miRNAs) are important regulators of gene expression and play a role in many biological processes. More than 700 human miRNAs have been identified so far with each having up to hundreds of unique target mRNAs. Computational tools, expression and proteomics assays, and chromatin-immunoprecipitation-based techniques provide important clues for identifying mRNAs that are direct targets of a particular miRNA. In addition, 3'UTR-reporter assays have become an important component of thorough miRNA target studies because they provide functional evidence for and quantitate the effects of specific miRNA-3'UTR interactions in a cell-based system. To enable more researchers to leverage 3'UTR-reporter assays and to support the scale-up of such assays to high-throughput levels, we have created a genome-wide collection of human 3'UTR luciferase reporters in the highly-optimized LightSwitch Luciferase Assay System. The system also includes synthetic miRNA target reporter constructs for use as positive controls, various endogenous 3'UTR reporter constructs, and a series of standardized experimental protocols. Here we describe a method for co-transfection of individual 3'UTR-reporter constructs along with a miRNA mimic that is efficient, reproducible, and amenable to high-throughput analysis.
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