Global Analyses of the Effect of Different Cellular Contexts on MicroRNA Targeting
Author(s)
Nam, Jin-Wu; Rissland, Olivia S.; Abreu-Goodger, Cei; Jan, Calvin H.; Agarwal, Vikram; Yildirim, Muhammed A.; Rodriguez, Antony; Koppstein, David Neal Pira; Bartel, David; Rissland, Olivia S.; Jan, Calvin H.; Yildirim, Muhammed A.; ... Show more Show less
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MicroRNA (miRNA) regulation clearly impacts animal development, but the extent to which development—with its resulting diversity of cellular contexts—impacts miRNA regulation is unclear. Here, we compared cohorts of genes repressed by the same miRNAs in different cell lines and tissues and found that target repertoires were largely unaffected, with secondary effects explaining most of the differential responses detected. Outliers resulting from differential direct targeting were often attributable to alternative 3′ UTR isoform usage that modulated the presence of miRNA sites. More inclusive examination of alternative 3′ UTR isoforms revealed that they influence ~10% of predicted targets when comparing any two cell types. Indeed, considering alternative 3′ UTR isoform usage improved prediction of targeting efficacy significantly beyond the improvements observed when considering constitutive isoform usage. Thus, although miRNA targeting is remarkably consistent in different cell types, considering the 3′ UTR landscape helps predict targeting efficacy and explain differential regulation that is observed.
Date issued
2014-03Department
Massachusetts Institute of Technology. Computational and Systems Biology Program; Massachusetts Institute of Technology. Department of Biology; Whitehead Institute for Biomedical ResearchJournal
Molecular Cell
Publisher
Elsevier
Citation
Nam, Jin-Wu, Olivia S. Rissland, David Koppstein, Cei Abreu-Goodger, Calvin H. Jan, Vikram Agarwal, Muhammed A. Yildirim, Antony Rodriguez, and David P. Bartel. “Global Analyses of the Effect of Different Cellular Contexts on MicroRNA Targeting.” Molecular Cell 53, no. 6 (March 2014): 1031–1043. © 2014 Elsevier Inc.
Version: Final published version
ISSN
10972765
1097-4164