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Distinct and separable roles for EZH2 in neurogenic astroglia.

Authors :
Hwang WW
Salinas RD
Siu JJ
Kelley KW
Delgado RN
Paredes MF
Alvarez-Buylla A
Oldham MC
Lim DA
Source :
ELife [Elife] 2014 May 27; Vol. 3, pp. e02439. Date of Electronic Publication: 2014 May 27.
Publication Year :
2014

Abstract

The epigenetic mechanisms that enable specialized astrocytes to retain neurogenic competence throughout adult life are still poorly understood. Here we show that astrocytes that serve as neural stem cells (NSCs) in the adult mouse subventricular zone (SVZ) express the histone methyltransferase EZH2. This Polycomb repressive factor is required for neurogenesis independent of its role in SVZ NSC proliferation, as Ink4a/Arf-deficiency in Ezh2-deleted SVZ NSCs rescues cell proliferation, but neurogenesis remains defective. Olig2 is a direct target of EZH2, and repression of this bHLH transcription factor is critical for neuronal differentiation. Furthermore, Ezh2 prevents the inappropriate activation of genes associated with non-SVZ neuronal subtypes. In the human brain, SVZ cells including local astroglia also express EZH2, correlating with postnatal neurogenesis. Thus, EZH2 is an epigenetic regulator that distinguishes neurogenic SVZ astrocytes, orchestrating distinct and separable aspects of adult stem cell biology, which has important implications for regenerative medicine and oncogenesis.DOI: http://dx.doi.org/10.7554/eLife.02439.001.

Details

Language :
English
ISSN :
2050-084X
Volume :
3
Database :
MEDLINE
Journal :
ELife
Publication Type :
Academic Journal
Accession number :
24867641
Full Text :
https://doi.org/10.7554/eLife.02439