Experimental strategies for microRNA target identification

被引:417
作者
Thomson, Daniel W. [1 ,2 ]
Bracken, Cameron P. [1 ,2 ]
Goodall, Gregory J. [1 ,2 ]
机构
[1] SA Pathol, Ctr Canc Biol, Adelaide, SA 5000, Australia
[2] Univ Adelaide, Dept Med, Adelaide, SA 5005, Australia
基金
英国医学研究理事会;
关键词
TRANSCRIPTOME-WIDE IDENTIFICATION; RNA-BINDING PROTEINS; MESSENGER-RNAS; MIRNA TARGETS; TRANSLATIONAL REPRESSION; CAENORHABDITIS-ELEGANS; PARALLEL ANALYSIS; MAMMALIAN-CELLS; CLEAVAGE; GENES;
D O I
10.1093/nar/gkr330
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
MicroRNAs (miRNAs) are important regulators of eukaryotic gene expression in most biological processes. They act by guiding the RNAi-induced silencing complex (RISC) to partially complementary sequences in target mRNAs to suppress gene expression by a combination of translation inhibition and mRNA decay. The commonly accepted mechanism of miRNA targeting in animals involves an interaction between the 5'-end of the miRNA called the 'seed region' and the 3' untranslated region (3'-UTR) of the mRNA. Many target prediction algorithms are based around such a model, though increasing evidence demonstrates that targeting can also be mediated through sites other than the 3'-UTR and that seed region base pairing is not always required. The power and validity of such in silico data can be therefore hindered by the simplified rules used to represent targeting interactions. Experimentation is essential to identify genuine miRNA targets, however many experimental modalities exist and their limitations need to be understood. This review summarizes and critiques the existing experimental techniques for miRNA target identification.
引用
收藏
页码:6845 / 6853
页数:9
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