A C. elegans genome-scale microRNA network contains composite feedback motifs with high flux capacity

  1. Natalia J. Martinez1,2,
  2. Maria C. Ow2,
  3. M. Inmaculada Barrasa1,2,
  4. Molly Hammell2,
  5. Reynaldo Sequerra3,
  6. Lynn Doucette-Stamm3,
  7. Frederick P. Roth4,
  8. Victor R. Ambros2, and
  9. Albertha J.M. Walhout1,2,5
  1. 1 Program in Gene Function and Expression, University of Massachusetts Medical School, Worcester, Massachusetts 01605, USA;
  2. 2 Program in Molecular Medicine, University of Massachusetts Medical School, Worcester, Massachusetts 01605, USA;
  3. 3 Agencourt Bioscience Corporation, Beverly, Massachusetts 01915, USA;
  4. 4 Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, Massachusetts 02115, USA

Abstract

MicroRNAs (miRNAs) and transcription factors (TFs) are primary metazoan gene regulators. Whereas much attention has focused on finding the targets of both miRNAs and TFs, the transcriptional networks that regulate miRNA expression remain largely unexplored. Here, we present the first genome-scale Caenorhabditis elegans miRNA regulatory network that contains experimentally mapped transcriptional TF → miRNA interactions, as well as computationally predicted post-transcriptional miRNA → TF interactions. We find that this integrated miRNA network contains 23 miRNA ↔ TF composite feedback loops in which a TF that controls a miRNA is itself regulated by that same miRNA. By rigorous network randomizations, we show that such loops occur more frequently than expected by chance and, hence, constitute a genuine network motif. Interestingly, miRNAs and TFs in such loops are heavily regulated and regulate many targets. This “high flux capacity” suggests that loops provide a mechanism of high information flow for the coordinate and adaptable control of miRNA and TF target regulons.

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