DAZL regulates Tet1 translation in murine embryonic stem cells

Embryonic stem cell (ESC) cultures display a heterogeneous gene expression profile, ranging from a pristine naïve pluripotent state to a primed epiblast state. Addition of inhibitors of GSK3β and MEK (so‐called 2i conditions) pushes ESC cultures toward a more homogeneous naïve pluripotent state, but...

Full description

Saved in:
Bibliographic Details
Published inEMBO reports Vol. 16; no. 7; pp. 791 - 802
Main Authors Welling, Maaike, Chen, Hsu-Hsin, Muñoz, Javier, Musheev, Michael U, Kester, Lennart, Junker, Jan Philipp, Mischerikow, Nikolai, Arbab, Mandana, Kuijk, Ewart, Silberstein, Lev, Kharchenko, Peter V, Geens, Mieke, Niehrs, Christof, van de Velde, Hilde, van Oudenaarden, Alexander, Heck, Albert JR, Geijsen, Niels
Format Journal Article
LanguageEnglish
Published London Blackwell Publishing Ltd 01.07.2015
Nature Publishing Group UK
John Wiley & Sons, Ltd
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Embryonic stem cell (ESC) cultures display a heterogeneous gene expression profile, ranging from a pristine naïve pluripotent state to a primed epiblast state. Addition of inhibitors of GSK3β and MEK (so‐called 2i conditions) pushes ESC cultures toward a more homogeneous naïve pluripotent state, but the molecular underpinnings of this naïve transition are not completely understood. Here, we demonstrate that DAZL, an RNA‐binding protein known to play a key role in germ‐cell development, marks a subpopulation of ESCs that is actively transitioning toward naïve pluripotency. Moreover, DAZL plays an essential role in the active reprogramming of cytosine methylation. We demonstrate that DAZL associates with mRNA of Tet1, a catalyst of 5‐hydroxylation of methyl‐cytosine, and enhances Tet1 mRNA translation. Overexpression of DAZL in heterogeneous ESC cultures results in elevated TET1 protein levels as well as increased global hydroxymethylation. Conversely, null mutation of Dazl severely stunts 2i‐mediated TET1 induction and hydroxymethylation. Our results provide insight into the regulation of the acquisition of naïve pluripotency and demonstrate that DAZL enhances TET1‐mediated cytosine hydroxymethylation in ESCs that are actively reprogramming to a pluripotent ground state. Synopsis This study reports that by enhancing Tet1 mRNA translation, the RNA‐binding protein DAZL regulates TET1‐mediated cytosine hydroxymethylation in ESCs during active reprogramming to a pluripotent ground state. DAZL marks ESCs actively transitioning to a naïve pluripotent state. DAZL enhances Tet1 mRNA translation. DAZL overexpression results in increased hydroxymethylation. Graphical Abstract This study reports that by enhancing Tet1 mRNA translation, the RNA‐binding protein DAZL regulates TET1‐mediated cytosine hydroxymethylation in ESCs during active reprogramming to a pluripotent ground state.
Bibliography:Netherlands Institute for Regenerative Medicine
istex:DB274E8A84C7A9D3F117F250F70F8A02304B0EEC
Netherlands Proteomics Centre
ArticleID:EMBR201540538
ark:/67375/WNG-MW17QTTN-R
AppendixTable EV1Table EV2Table EV3Table EV4Table EV5Table EV6Review Process File
The Netherlands Organization for Scientific Research (NWO) - No. 91796323
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
Research Institute of Molecular Pathology, Mass Spectrometry & Protein Chemistry, Vienna, Austria
Present address: Proteomics Unit, Spanish National Cancer Research Centre (CNIO), Madrid, Spain
These authors contributed equally to this manuscript
Subject Categories Stem Cells
ISSN:1469-221X
1469-3178
DOI:10.15252/embr.201540538