A role for the Werner syndrome protein in epigenetic inactivation of the pluripotency factor Oct4.
Aging Cell
; 9(4): 580-91, 2010 Aug.
Article
in En
| MEDLINE
| ID: mdl-20477760
ABSTRACT
Werner syndrome (WS) is an autosomal recessive disorder, the hallmarks of which are premature aging and early onset of neoplastic diseases (Orren, 2006; Bohr, 2008). The gene, whose mutation underlies the WS phenotype, is called WRN. The protein encoded by the WRN gene, WRNp, has DNA helicase activity (Gray et al., 1997; Orren, 2006; Bohr, 2008; Opresko, 2008). Extensive evidence suggests that WRNp plays a role in DNA replication and DNA repair (Chen et al., 2003; Hickson, 2003; Orren, 2006; Turaga et al., 2007; Bohr, 2008). However, WRNp function is not yet fully understood. In this study, we show that WRNp is involved in de novo DNA methylation of the promoter of the Oct4 gene, which encodes a crucial stem cell transcription factor. We demonstrate that WRNp localizes to the Oct4 promoter during retinoic acid-induced differentiation of human pluripotent cells and associates with the de novo methyltransferase Dnmt3b in the chromatin of differentiating pluripotent cells. Depletion of WRNp does not affect demethylation of lysine 4 of the histone H3 at the Oct4 promoter, nor methylation of lysine 9 of H3, but it blocks the recruitment of Dnmt3b to the promoter and results in the reduced methylation of CpG sites within the Oct4 promoter. The lack of DNA methylation was associated with continued, albeit greatly reduced, Oct4 expression in WRN-deficient, retinoic acid-treated cells, which resulted in attenuated differentiation. The presented results reveal a novel function of WRNp and demonstrate that WRNp controls a key step in pluripotent stem cell differentiation.
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Gene Silencing
/
Pluripotent Stem Cells
/
Epigenesis, Genetic
/
Octamer Transcription Factor-3
/
Exodeoxyribonucleases
/
RecQ Helicases
Type of study:
Prognostic_studies
Limits:
Humans
Language:
En
Journal:
Aging Cell
Year:
2010
Document type:
Article
Affiliation country:
United States