共 26 条
Tandem affinity purification of miRNA target mRNAs (TAP-Tar)
被引:45
作者:

Nonne, Nora
论文数: 0 引用数: 0
h-index: 0
机构: Inst Andre Lwoff, CNRS, FRE 2944, F-94801 Villejuif, France

Ameyar-Zazoua, Maya
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h-index: 0
机构: Inst Andre Lwoff, CNRS, FRE 2944, F-94801 Villejuif, France

Souidi, Mouloud
论文数: 0 引用数: 0
h-index: 0
机构: Inst Andre Lwoff, CNRS, FRE 2944, F-94801 Villejuif, France

Harel-Bellan, Annick
论文数: 0 引用数: 0
h-index: 0
机构:
Inst Andre Lwoff, CNRS, FRE 2944, F-94801 Villejuif, France Inst Andre Lwoff, CNRS, FRE 2944, F-94801 Villejuif, France
机构:
[1] Inst Andre Lwoff, CNRS, FRE 2944, F-94801 Villejuif, France
关键词:
MICRORNA TARGETS;
IDENTIFICATION;
BIOGENESIS;
MECHANISMS;
CLEAVAGE;
SIRNAS;
CELLS;
D O I:
10.1093/nar/gkp1100
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) bind to Argonaute proteins, and together they form the RISC complex and regulate target mRNA translation and/or stability. Identification of mRNA targets is key to deciphering the physiological functions and mode of action of miRNAs. In mammals, miRNAs are generally poorly homologous to their target sequence, and target identification cannot be based solely on bioinformatics. Here, we describe a biochemical approach, based on tandem affinity purification, in which mRNA/miRNA complexes are sequentially pulled down, first via the Argonaute moiety and then via the miRNA. Our 'TAP-Tar' procedure allows the specific pull down of mRNA targets of miRNA. It is useful for validation of targets predicted in silico, and, potentially, for discovery of previously uncharacterized targets.
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页码:e20.1 / e20.5
页数:5
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