Loss of functional Dicer in mouse radial glia cell-autonomously prolongs cortical neurogenesis

Dev Biol. 2013 Oct 15;382(2):530-7. doi: 10.1016/j.ydbio.2013.08.023. Epub 2013 Sep 5.

Abstract

Radial glia of the mouse cerebral cortex emerge from neuroepithelial stem cells around embryonic day 11 and produce excitatory cortical neurons until a few days before birth. The molecular mechanisms that regulate the end of cortical neurogenesis remain largely unknown. Here we investigated if the Dicer-dependent microRNA (miRNA) pathway is involved. By electroporating a cre-recombinase expression vector into the cortex of E13.5 embryos carrying a conditional allele of Dicer1, we induced mosaic recombination causing Dicer1 deletion and reporter activation in a subset of radial glia. We analysed the long-term fates of their progeny. We found that mutant radial glia produced abnormally large numbers of Cux1-positive neurons, many of which populated the superficial cortical layers. Injections of the S-phase marker bromodeoxyuridine between postnatal days 3 and 14 showed that much of this population was generated postnatally. Our findings suggest a role for Dicer-dependent processes in limiting the timespan of cortical neurogenesis.

Keywords: Dicer; Mouse; Neurogenesis; Telencephalon; microRNA.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cerebral Cortex / cytology*
  • Cerebral Cortex / embryology
  • Cerebral Cortex / growth & development
  • DEAD-box RNA Helicases / genetics*
  • Embryo, Mammalian / metabolism
  • Mice
  • MicroRNAs / metabolism
  • Neurogenesis / genetics*
  • Neuroglia / physiology*
  • Neurons / cytology*
  • Neurons / metabolism
  • Ribonuclease III / genetics*
  • Stem Cells / cytology
  • Stem Cells / metabolism

Substances

  • MicroRNAs
  • Dicer1 protein, mouse
  • Ribonuclease III
  • DEAD-box RNA Helicases