Functional regulation of FoxO1 in neural stem cell differentiation

Cell Death Differ. 2015 Dec;22(12):2034-45. doi: 10.1038/cdd.2015.123. Epub 2015 Oct 16.

Abstract

Forkhead transcription factor family O (FoxO) maintains adult stem cell reserves by supporting their long-term proliferative potential. MicroRNAs (miRs) regulate neuronal stem/progenitor cell (NSPC) proliferation and differentiation during neural development by controlling the expression of a specific set of target genes. In the neurogenic subventricular zone, FoxO1 is specifically expressed in NSPCs and is no longer detected during the transition to neuroblast stage, forming an inverse correlation with miR-9 expression. The 3'-untranslated region of FoxO1 contains a conserved target sequence of miR-9 and FoxO1 expression is coordinated in concert with miR-9 during neuronal differentiation. Our study demonstrates that FoxO1 contributes to NSPC fate decision through its cooperation with the Notch signaling pathway.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3' Untranslated Regions
  • Animals
  • Base Sequence
  • Cell Differentiation
  • Cells, Cultured
  • Doublecortin Domain Proteins
  • Forkhead Box Protein O1
  • Forkhead Transcription Factors / chemistry
  • Forkhead Transcription Factors / genetics
  • Forkhead Transcription Factors / metabolism*
  • Mice
  • MicroRNAs / genetics
  • MicroRNAs / metabolism
  • Microtubule-Associated Proteins / genetics
  • Microtubule-Associated Proteins / metabolism
  • Nestin / genetics
  • Nestin / metabolism
  • Neural Stem Cells / cytology
  • Neural Stem Cells / metabolism
  • Neuropeptides / genetics
  • Neuropeptides / metabolism
  • Receptors, Notch / genetics
  • Receptors, Notch / metabolism
  • Sequence Alignment
  • Signal Transduction
  • Tubulin / genetics
  • Tubulin / metabolism

Substances

  • 3' Untranslated Regions
  • Doublecortin Domain Proteins
  • Forkhead Box Protein O1
  • Forkhead Transcription Factors
  • Foxo1 protein, mouse
  • MIRN9 microRNA, mouse
  • MicroRNAs
  • Microtubule-Associated Proteins
  • Nestin
  • Neuropeptides
  • Receptors, Notch
  • Tubulin