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

Author:

Urbán Noelia1,van den Berg Debbie L. C.1,Forget Antoine23,Andersen Jimena1,Demmers Jeroen A. A.4,Hunt Charles1,Ayrault Olivier23,Guillemot François1

Affiliation:

1. The Francis Crick Institute–Mill Hill Laboratory, NW7 1AA, London, UK.

2. Institut Curie, PSL Research University, CNRS UMR 3347, INSERM U1021, 91405, Orsay, France.

3. Université Paris Sud, Université Paris Saclay, CNRS UMR 3347, INSERM U1021, 91405, Orsay, France.

4. Proteomics Center, Erasmus MC, Wytemaweg 80, 3015 CN Rotterdam, Netherlands.

Abstract

Sending neural stem cells back to the garage In the brain's hippocampus, which modulates memories and emotions, neural stem cells generate new neurons, even during adulthood. How many new neurons are generated, and when, follows from the balance between quiescence and proliferation in the pool of neural stem cells. Urbán et al. asked what signals send proliferating stem cells back into a quiescent state. They found that a key transcription factor that promotes cellular proliferation was degraded through the ubiquitinylation system. This molecular interaction regulated the return to a resting state, but one that was not quite as quiescent as the original state. Stem cells in this resting but primed state sustained the stem cell pool. Science , this issue p. 292

Funder

Medical Research Council (MRC)

Federation of European Biochemical Societies

Netherlands Organisation for Scientific Research (NWO)

Fondation de France

Wellcome Trust

Biotechnology and Biological Sciences Research Council

MRC

Francis Crick Institute

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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