MiR-375 is Essential for Human Spinal Motor Neuron Development and May Be Involved in Motor Neuron Degeneration

Stem Cells. 2016 Jan;34(1):124-34. doi: 10.1002/stem.2233. Epub 2015 Nov 20.

Abstract

The transcription factor REST is a key suppressor of neuronal genes in non-neuronal tissues. REST has been shown to suppress proneuronal microRNAs in neural progenitors indicating that REST-mediated neurogenic suppression may act in part via microRNAs. We used neural differentiation of Rest-null mouse ESC to identify dozens of microRNAs regulated by REST during neural development. One of the identified microRNAs, miR-375, was upregulated during human spinal motor neuron development. We found that miR-375 facilitates spinal motor neurogenesis by targeting the cyclin kinase CCND2 and the transcription factor PAX6. Additionally, miR-375 inhibits the tumor suppressor p53 and protects neurons from apoptosis in response to DNA damage. Interestingly, motor neurons derived from a spinal muscular atrophy patient displayed depressed miR-375 expression and elevated p53 protein levels. Importantly, SMA motor neurons were significantly more susceptible to DNA damage induced apoptosis suggesting that miR-375 may play a protective role in motor neurons.

Keywords: CCND2; Motor neuron; PAX6/REST; miR-375.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis / genetics
  • Base Sequence
  • Humans
  • Mice
  • MicroRNAs / genetics*
  • MicroRNAs / metabolism
  • Molecular Sequence Data
  • Motor Neurons / metabolism*
  • Motor Neurons / pathology*
  • Muscular Atrophy, Spinal / genetics
  • Nerve Degeneration / genetics
  • Nerve Degeneration / pathology*
  • Neurogenesis / genetics
  • Signal Transduction / genetics
  • Tumor Suppressor Protein p53 / metabolism

Substances

  • MIRN375 microRNA, human
  • MicroRNAs
  • Tumor Suppressor Protein p53