| Literature DB >> 33909924 |
Daniel Olivieri1, Eleonora Castelli1,2, Yumiko K Kawamura1, Panagiotis Papasaikas1,3, Ilya Lukonin1, Melanie Rittirsch1, Daniel Hess1, Sébastien A Smallwood1, Michael B Stadler1,3, Antoine H F M Peters1,2, Joerg Betschinger1.
Abstract
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.Entities:
Keywords: Dax1/Nr0b1; Hdac3; embryonic stem cell; extraembryonic endoderm; pluripotency
Mesh:
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Year: 2021 PMID: 33909924 PMCID: PMC8204867 DOI: 10.15252/embj.2020106818
Source DB: PubMed Journal: EMBO J ISSN: 0261-4189 Impact factor: 14.012