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Cooperation between HDAC3 and DAX1 mediates lineage restriction of embryonic stem cells.
Olivieri, Daniel; Castelli, Eleonora; Kawamura, Yumiko K; Papasaikas, Panagiotis; Lukonin, Ilya; Rittirsch, Melanie; Hess, Daniel; Smallwood, Sébastien A; Stadler, Michael B; Peters, Antoine H F M; Betschinger, Joerg.
Affiliation
  • Olivieri D; Friedrich Miescher Institute for Biomedical Research, Basel, Switzerland.
  • Castelli E; Friedrich Miescher Institute for Biomedical Research, Basel, Switzerland.
  • Kawamura YK; Faculty of Sciences, University of Basel, Basel, Switzerland.
  • Papasaikas P; Friedrich Miescher Institute for Biomedical Research, Basel, Switzerland.
  • Lukonin I; Friedrich Miescher Institute for Biomedical Research, Basel, Switzerland.
  • Rittirsch M; Swiss Institute of Bioinformatics, Basel, Switzerland.
  • Hess D; Friedrich Miescher Institute for Biomedical Research, Basel, Switzerland.
  • Smallwood SA; Friedrich Miescher Institute for Biomedical Research, Basel, Switzerland.
  • Stadler MB; Friedrich Miescher Institute for Biomedical Research, Basel, Switzerland.
  • Peters AHFM; Friedrich Miescher Institute for Biomedical Research, Basel, Switzerland.
  • Betschinger J; Friedrich Miescher Institute for Biomedical Research, Basel, Switzerland.
EMBO J ; 40(12): e106818, 2021 06 15.
Article in En | MEDLINE | ID: mdl-33909924
Mouse embryonic stem cells (mESCs) are biased toward producing embryonic rather than extraembryonic endoderm fates. Here, we identify the mechanism of this barrier and report that the histone deacetylase Hdac3 and the transcriptional corepressor Dax1 cooperatively limit the lineage repertoire of mESCs by silencing an enhancer of the extraembryonic endoderm-specifying transcription factor Gata6. This restriction is opposed by the pluripotency transcription factors Nr5a2 and Esrrb, which promote cell type conversion. Perturbation of the barrier extends mESC potency and allows formation of 3D spheroids that mimic the spatial segregation of embryonic epiblast and extraembryonic endoderm in early embryos. Overall, this study shows that transcriptional repressors stabilize pluripotency by biasing the equilibrium between embryonic and extraembryonic lineages that is hardwired into the mESC transcriptional network.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: DAX-1 Orphan Nuclear Receptor / Mouse Embryonic Stem Cells / Histone Deacetylases Type of study: Prognostic_studies Limits: Animals Language: En Journal: EMBO J Year: 2021 Type: Article Affiliation country: Switzerland

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: DAX-1 Orphan Nuclear Receptor / Mouse Embryonic Stem Cells / Histone Deacetylases Type of study: Prognostic_studies Limits: Animals Language: En Journal: EMBO J Year: 2021 Type: Article Affiliation country: Switzerland