Abstract
MicroRNAs coordinate networks of mRNAs, but predicting specific sites of interactions is complicated by the very few bases of complementarity needed for regulation. Although efforts to characterize the specific requirements for microRNA (miR) regulation have made some advances, no general model of target recognition has been widely accepted. In this work, we describe an entirely novel approach to miR target identification. The genomic events responsible for the creation of individual miR loci have now been described with many miRs now known to have been initially formed from transposable element (TE) sequences. In light of this, we propose that limiting miR target searches to transcripts containing a miR’s progenitor TE can facilitate accurate target identification. In this report we outline the methodology behind OrbId (Origin-based identification of microRNA targets). In stark contrast to the principal miR target algorithms (which rely heavily on target site conservation across species and are therefore...
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CITATION STYLE
Filshtein, T. J., Mackenzie, C. O., Dale, M. D., Dela-Cruz, P. S., Ernst, D. M., Frankenberger, E. A., … Larson, E. D. (2012). OrbId. Mobile Genetic Elements, 2(4), 184–192. https://doi.org/10.4161/mge.21617
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