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

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 mo...

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Veröffentlicht in:Science (American Association for the Advancement of Science) 2016-07, Vol.353 (6296), p.292-295
Hauptverfasser: Urbán, Noelia, van den Berg, Debbie L. C., Forget, Antoine, Andersen, Jimena, Demmers, Jeroen A. A., Hunt, Charles, Ayrault, Olivier, Guillemot, François
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Sprache:eng
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Zusammenfassung: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 AscI1 (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.
ISSN:0036-8075
1095-9203
DOI:10.1126/science.aaf4802