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

Authors :
Urbán N
van den Berg DL
Forget A
Andersen J
Demmers JA
Hunt C
Ayrault O
Guillemot F
Source :
Science (New York, N.Y.) [Science] 2016 Jul 15; Vol. 353 (6296), pp. 292-5.
Publication Year :
2016

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.<br /> (Copyright © 2016, American Association for the Advancement of Science.)

Details

Language :
English
ISSN :
1095-9203
Volume :
353
Issue :
6296
Database :
MEDLINE
Journal :
Science (New York, N.Y.)
Publication Type :
Academic Journal
Accession number :
27418510
Full Text :
https://doi.org/10.1126/science.aaf4802