Reference : MicroRNAs control de novo DNA methylation through regulation of transcriptional repre...
Scientific journals : Article
Life sciences : Biochemistry, biophysics & molecular biology
http://hdl.handle.net/10993/247
MicroRNAs control de novo DNA methylation through regulation of transcriptional repressors in mouse embryonic stem cells
English
Sinkkonen, Lasse mailto [Friederich Miescher Institute for Biomedical Research > Epigenetics]
Hugenschmidt, Tabea [Friederich Miescher Institute for Biomedical Research > Epigenetics]
Berninger, Philipp [University of Basel > Biozentrum]
Gaidatzis, Dimos [University of Basel > Biozentrum]
Mohn, Fabio [Friederich Miescher Institute for Biomedical Research]
Artus-Revel, Caroline G. [Friederich Miescher Institute for Biomedical Research]
Zavolan, Mihaela [University of Basel > Biozentrum]
Svoboda, Petr [Friederich Miescher Institute for Biomedical Research]
Filipowicz, Witold [Friederich Miescher Institute for Biomedical Research]
Mar-2008
Nature Structural & Molecular Biology
Nature Publishing Group
15
3
259-67
Yes (verified by ORBilu)
International
1545-9993
1545-9985
[en] Loss of microRNA (miRNA) pathway components negatively affects differentiation of embryonic stem (ES) cells, but the underlying molecular mechanisms remain poorly defined. Here we characterize changes in mouse ES cells lacking Dicer (Dicer1). Transcriptome analysis of Dicer-/- cells indicates that the ES-specific miR-290 cluster has an important regulatory function in undifferentiated ES cells. Consistently, many of the defects in Dicer-deficient cells can be reversed by transfection with miR-290 family miRNAs. We demonstrate that Oct4 (also known as Pou5f1) silencing in differentiating Dicer-/- ES cells is accompanied by accumulation of repressive histone marks but not by DNA methylation, which prevents the stable repression of Oct4. The methylation defect correlates with downregulation of de novo DNA methyltransferases (Dnmts). The downregulation is mediated by Rbl2 and possibly other transcriptional repressors, potential direct targets of miR-290 cluster miRNAs. The defective DNA methylation can be rescued by ectopic expression of de novo Dnmts or by transfection of the miR-290 cluster miRNAs, indicating that de novo DNA methylation in ES cells is controlled by miRNAs.
http://hdl.handle.net/10993/247
10.1038/nsmb.1391
http://www.nature.com/nsmb/journal/v15/n3/full/nsmb.1391.html

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