Return to quiescence of mouse neural stem cells by degradation of a proactivation protein
journal contributionposted on 02.10.2020 by Noelia Urbán, Debbie LC van den Berg, Antoine Forget, Jimena Andersen, Jeroen AA Demmers, Charles Hunt, Olivier Ayrault, François Guillemot
Any type of content formally published in an academic journal, usually following a peer-review process.
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.