Return to quiescence of mouse neural stem cells by degradation of a proactivation protein

Science. 2016 Jul 15;353(6296):292-5. doi: 10.1126/science.aaf4802.

Abstract

Quiescence is essential for long-term maintenance of adult stem cells. Niche signals regulate the transit of stem cells from dormant to activated states. Here, we show that the E3-ubiquitin ligase Huwe1 (HECT, UBA, and WWE domain-containing 1) is required for proliferating stem cells of the adult mouse hippocampus to return to quiescence. Huwe1 destabilizes proactivation protein Ascl1 (achaete-scute family bHLH transcription factor 1) in proliferating hippocampal stem cells, which prevents accumulation of cyclin Ds and promotes the return to a resting state. When stem cells fail to return to quiescence, the proliferative stem cell pool becomes depleted. Thus, long-term maintenance of hippocampal neurogenesis depends on the return of stem cells to a transient quiescent state through the rapid degradation of a key proactivation factor.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult Stem Cells / cytology
  • Adult Stem Cells / metabolism
  • Adult Stem Cells / physiology*
  • Animals
  • Basic Helix-Loop-Helix Transcription Factors / metabolism
  • Cell Proliferation
  • Hippocampus / cytology
  • Hippocampus / embryology*
  • Mice
  • Mice, Knockout
  • Neural Stem Cells / cytology
  • Neural Stem Cells / metabolism
  • Neural Stem Cells / physiology*
  • Neurogenesis*
  • Protein Stability
  • Proteolysis
  • Tumor Suppressor Proteins
  • Ubiquitin-Protein Ligases / genetics
  • Ubiquitin-Protein Ligases / metabolism*

Substances

  • Ascl1 protein, mouse
  • Basic Helix-Loop-Helix Transcription Factors
  • Tumor Suppressor Proteins
  • Huwe1 protein, mouse
  • Ubiquitin-Protein Ligases