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Rapid identification of regulatory microRNAs by miTRAP (miRNA trapping by RNA in vitro affinity purification)
被引:44
作者:

Braun, Juliane
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机构:
Univ Halle Wittenberg, Mol Cell Biol Div, Inst Mol Med, D-06120 Halle, Germany Univ Halle Wittenberg, Mol Cell Biol Div, Inst Mol Med, D-06120 Halle, Germany

Misiak, Danny
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Univ Halle Wittenberg, Mol Cell Biol Div, Inst Mol Med, D-06120 Halle, Germany Univ Halle Wittenberg, Mol Cell Biol Div, Inst Mol Med, D-06120 Halle, Germany

Busch, Bianca
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机构:
Univ Halle Wittenberg, Mol Cell Biol Div, Inst Mol Med, D-06120 Halle, Germany Univ Halle Wittenberg, Mol Cell Biol Div, Inst Mol Med, D-06120 Halle, Germany

Krohn, Knut
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机构:
Univ Leipzig, Interdisciplinary Ctr Clin Res, D-04103 Leipzig, Germany Univ Halle Wittenberg, Mol Cell Biol Div, Inst Mol Med, D-06120 Halle, Germany

Huettelmaier, Stefan
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Univ Halle Wittenberg, Mol Cell Biol Div, Inst Mol Med, D-06120 Halle, Germany Univ Halle Wittenberg, Mol Cell Biol Div, Inst Mol Med, D-06120 Halle, Germany
机构:
[1] Univ Halle Wittenberg, Mol Cell Biol Div, Inst Mol Med, D-06120 Halle, Germany
[2] Univ Leipzig, Interdisciplinary Ctr Clin Res, D-04103 Leipzig, Germany
关键词:
DIFFERENTIAL EXPRESSION ANALYSIS;
C-MYC EXPRESSION;
MESSENGER-RNA;
BIOCONDUCTOR PACKAGE;
FEEDBACK LOOP;
BINDING;
TARGETS;
SUPPRESSION;
RECOGNITION;
PROTEINS;
D O I:
10.1093/nar/gku127
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) control gene expression at the post-transcriptional level. However, the identification of miRNAs regulating the fate of a specific messenger RNA remains limited due to the imperfect complementarity of miRNAs and targeted transcripts. Here, we describe miTRAP (miRNA trapping by RNA in vitro affinity purification), an advanced protocol of previously reported MS2-tethering approaches. MiTRAP allows the rapid identification of miRNAs targeting an in vitro transcribed RNA in cell lysates. Selective co-purification of regulatory miRNAs was confirmed for the MYC- as well as ZEB2-3'UTR, two well-established miRNA targets in vivo. Combined with miRNA-sequencing, miTRAP identified in addition to miRNAs reported to control MYC expression, 18 novel candidates including not in silico predictable miRNAs. The evaluation of 10 novel candidate miRNAs confirmed 3'UTR-dependent regulation of MYC expression as well as putative non-canonical targeting sites for the not in silico predictable candidates. In conclusion, miTRAP provides a rapid, cost-effective and easy-to-handle protocol allowing the identification of regulatory miRNAs for RNAs of choice in a cellular context of interest. Most notably, miTRAP not only identifies in silico predictable but also unpredictable miRNAs regulating the expression of a specific target RNA.
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