Author:
Pais Helio,Nicolas Francisco Esteban,Soond Surinder M.,Swingler Tracey E.,Clark Ian M.,Chantry Andrew,Moulton Vincent,Dalmay Tamas
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.
Publisher
Cold Spring Harbor Laboratory
Cited by
108 articles.
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