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.

doi.org/10.1126/science.aaf4802, hdl.handle.net/1765/97653
Science
Erasmus MC: University Medical Center Rotterdam

Urbán, N. (Noelia), van den Berg, D., Forget, A. (Antoine), Andersen, J. (Jimena), Demmers, J., Hunt, C. (Charles), … Guillemot, F. (2016). Return to Quiescence of mouse neural stem cells by degradation of a proactivation protein. Science, 353(6296), 292–295. doi:10.1126/science.aaf4802