Friedrich Miescher Institute for Biomedical Research, Basel, Switzerland.
Faculty of Sciences, University of Basel, Basel, Switzerland.
EMBO J. 2021 Jun 15;40(12):e106818. doi: 10.15252/embj.2020106818. Epub 2021 Apr 28.
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.
小鼠胚胎干细胞(mESCs)偏向于产生胚胎内胚层而不是胚胎外胚层命运。在这里,我们确定了这种障碍的机制,并报告组蛋白去乙酰化酶 Hdac3 和转录核心抑制因子 Dax1 通过沉默胚胎外胚层指定转录因子 Gata6 的增强子来共同限制 mESC 的谱系谱。这种限制与多能转录因子 Nr5a2 和 Esrrb 相反,它们促进细胞类型转换。屏障的破坏扩展了 mESC 的效力,并允许形成 3D 球体,模拟早期胚胎中胚胎上胚层和胚胎外胚层的空间分离。总的来说,这项研究表明,转录抑制剂通过偏向于胚胎内胚层和胚胎外胚层谱系之间的平衡来稳定多能性,这种平衡是硬连线到 mESC 转录网络中的。