A feedforward regulatory loop between HuR and the long noncoding RNA linc-MD1 controls early phases of myogenesis

Mol Cell. 2014 Feb 6;53(3):506-14. doi: 10.1016/j.molcel.2013.12.012. Epub 2014 Jan 16.

Abstract

The muscle-specific long noncoding RNA linc-MD1 was shown to be expressed during early phases of muscle differentiation and to trigger the switch to later stages by acting as a sponge for miR-133 and miR-135. Notably, linc-MD1 is also the host transcript of miR-133b, and their biogenesis is mutually exclusive. Here, we describe that this alternative synthesis is controlled by the HuR protein, which favors linc-MD1 accumulation through its ability to bind linc-MD1 and repress Drosha cleavage. We show that HuR is under the repressive control of miR-133 and that the sponging activity of linc-MD1 consolidates HuR expression in a feedforward positive loop. Finally, we show that HuR also acts in the cytoplasm, reinforcing linc-MD1 sponge activity by cooperating for miRNA recruitment. An increase in miR-133 synthesis, mainly from the two unrelated miR-133a coding genomic loci, is likely to trigger the exit from this circuitry and progression to later differentiation stages.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Differentiation
  • Cell Line
  • Cytoplasm / metabolism
  • ELAV Proteins / genetics
  • ELAV Proteins / metabolism
  • ELAV Proteins / physiology*
  • Feedback, Physiological
  • Mice
  • MicroRNAs / analysis
  • MicroRNAs / metabolism
  • Muscle Development / genetics*
  • RNA, Long Noncoding / genetics
  • RNA, Long Noncoding / metabolism
  • RNA, Long Noncoding / physiology*

Substances

  • ELAV Proteins
  • MicroRNAs
  • Mirn133 microRNA, mouse
  • RNA, Long Noncoding
  • long noncoding RNA, linc-MD1, mouse