Analyzing mRNA expression identifies Smad3 as a microRNA-140 target regulated only at protein level

  1. Tamas Dalmay2
  1. 1School of Computing Sciences, University of East Anglia, Norwich, NR4 7TJ, United Kingdom
  2. 2School of Biological Sciences, University of East Anglia, Norwich, NR4 7TJ, United Kingdom
  1. 3 These authors contributed equally to this work.

Abstract

mRNA profiling is routinely used to identify microRNA targets, however, this high-throughput technology is not suitable for identifying targets regulated only at protein level. Here, we have developed and validated a novel methodology based on computational analysis of promoter sequences combined with mRNA microarray experiments to reveal transcription factors that are direct microRNA targets at the protein level. Using this approach we identified Smad3, a key transcription factor in the TGFβ signaling pathway, as a direct miR-140 target. We showed that miR-140 suppressed the TGFβ pathway through repression of Smad3 and that TGFβ suppressed the accumulation of miR-140 forming a double negative feedback loop. Our findings establish a valid strategy for the discovery of microRNA targets regulated only at protein level, and we propose that additional targets could be identified by re-analysis of existing microarray datasets.

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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; or Vincent Moulton, School of Computing Sciences, University of East Anglia, Norwich, NR4 7TJ, United Kingdom; e-mail: v.moulton{at}uea.ac.uk; fax: 0044 1603 593345.

  • Article published online ahead of print. Article and publication date are at http://www.rnajournal.org/cgi/doi/10.1261/rna.1701210.

    • Received April 23, 2009.
    • Accepted November 23, 2009.
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