Experimental identification of microRNA-140 targets by silencing and overexpressing miR-140

  1. Francisco Esteban Nicolas1,5,
  2. Helio Pais2,5,
  3. Frank Schwach2,
  4. Morten Lindow3,
  5. Sakari Kauppinen3,4,
  6. Vincent Moulton2, and
  7. Tamas Dalmay1
  1. 1School of Biological Sciences, University of East Anglia, Norwich, NR4 7TJ, United Kingdom
  2. 2School of Computing Sciences, University of East Anglia, Norwich, NR4 7TJ, United Kingdom
  3. 3Santaris Pharma, DK-2970 Hørsholm, Denmark
  4. 4Wilhelm Johannsen Center for Functional Genome Research, Department of Cellular and Molecular Medicine, University of Copenhagen, DK-2200 Copenhagen N, Denmark
  1. 5 These authors contributed equally to this work.

Abstract

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.

Keywords

Footnotes

  • Reprint requests to: Tamas Dalmay, School of Biological Sciences, University of East Anglia, Norwich, NR4 7TJ, United Kingdom; e-mail: t.dalmay{at}uea.ac.uk; fax: 0044 1603 592250.

  • Article published online ahead of print. Article and publication date are at http://www.rnajournal.org/cgi/doi/10.1261/rna.1221108.

    • Received June 13, 2008.
    • Accepted September 3, 2008.
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