共 33 条
Experimental identification of microRNA-140 targets by silencing and overexpressing miR-140
被引:93
作者:

Nicolas, Francisco Esteban
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机构:
Univ E Anglia, Sch Biol Sci, Norwich NR4 7TJ, Norfolk, England Univ E Anglia, Sch Biol Sci, Norwich NR4 7TJ, Norfolk, England

Pais, Helio
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机构:
Univ E Anglia, Sch Comp Sci, Norwich NR4 7TJ, Norfolk, England Univ E Anglia, Sch Biol Sci, Norwich NR4 7TJ, Norfolk, England

Schwach, Frank
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机构:
Univ E Anglia, Sch Comp Sci, Norwich NR4 7TJ, Norfolk, England Univ E Anglia, Sch Biol Sci, Norwich NR4 7TJ, Norfolk, England

Lindow, Morten
论文数: 0 引用数: 0
h-index: 0
机构:
Santaris Pharma, DK-2970 Horsholm, Denmark Univ E Anglia, Sch Biol Sci, Norwich NR4 7TJ, Norfolk, England

Kauppinen, Sakari
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h-index: 0
机构:
Santaris Pharma, DK-2970 Horsholm, Denmark
Univ Copenhagen, Dept Cellular & Mol Med, Wilhelm Johannsen Ctr Funct Genome Res, DK-2200 Copenhagen, Denmark Univ E Anglia, Sch Biol Sci, Norwich NR4 7TJ, Norfolk, England

Moulton, Vincent
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h-index: 0
机构:
Univ E Anglia, Sch Comp Sci, Norwich NR4 7TJ, Norfolk, England Univ E Anglia, Sch Biol Sci, Norwich NR4 7TJ, Norfolk, England

Dalmay, Tamas
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h-index: 0
机构:
Univ E Anglia, Sch Biol Sci, Norwich NR4 7TJ, Norfolk, England Univ E Anglia, Sch Biol Sci, Norwich NR4 7TJ, Norfolk, England
机构:
[1] Univ E Anglia, Sch Biol Sci, Norwich NR4 7TJ, Norfolk, England
[2] Univ E Anglia, Sch Comp Sci, Norwich NR4 7TJ, Norfolk, England
[3] Santaris Pharma, DK-2970 Horsholm, Denmark
[4] Univ Copenhagen, Dept Cellular & Mol Med, Wilhelm Johannsen Ctr Funct Genome Res, DK-2200 Copenhagen, Denmark
来源:
基金:
英国医学研究理事会;
关键词:
microRNA;
target identification;
cartilage development;
D O I:
10.1261/rna.1221108
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 short noncoding RNA molecules regulating the expression of mRNAs. Target identification of miRNAs is computationally difficult due to the relatively low homology between miRNAs and their targets. We present here an experimental approach to target identification where the cartilage-specific miR-140 was overexpressed and silenced in cells it is normally expressed in separate experiments. Expression of mRNAs was profiled in both experiments and the intersection of mRNAs repressed by miR-140 overexpression and derepressed by silencing of miR-140 was identified. The intersection contained only 49 genes, although both treatments affected the accumulation of hundreds of mRNAs. These 49 genes showed a very strong enrichment for the miR-140 seed sequence implying that the approach is efficient and specific. Twenty-one of these 49 genes were predicted to be direct targets based on the presence of the seed sequence. Interestingly, none of these were predicted by the published target prediction methods we used. One of the potential target mRNAs, Cxcl12, was experimentally validated by Northern blot analysis and a luciferase reporter assay.
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收藏
页码:2513 / 2520
页数:8
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