MRC Human Genetics Unit, Institute of Genetics and Molecular Medicine, University of Edinburgh, Crewe Road South, Edinburgh EH4 2XU, UK.
MRC Human Genetics Unit, Institute of Genetics and Molecular Medicine, University of Edinburgh, Crewe Road South, Edinburgh EH4 2XU, UK; Northern Institute for Cancer Research, Framlington Place, Medical Faculty, Newcastle upon Tyne NE2 4HH, UK.
Cell Rep. 2019 Nov 12;29(7):1974-1985.e6. doi: 10.1016/j.celrep.2019.10.031.
The DNA hypomethylation that occurs when embryonic stem cells (ESCs) are directed to the ground state of naive pluripotency by culturing in two small molecule inhibitors (2i) results in redistribution of polycomb (H3K27me3) away from its target loci. Here, we demonstrate that 3D genome organization is also altered in 2i, with chromatin decompaction at polycomb target loci and a loss of long-range polycomb interactions. By preventing DNA hypomethylation during the transition to the ground state, we are able to restore to ESC in 2i the H3K27me3 distribution, as well as polycomb-mediated 3D genome organization that is characteristic of primed ESCs grown in serum. However, these cells retain the functional characteristics of 2i ground-state ESCs. Our findings demonstrate the central role of DNA methylation in shaping major aspects of 3D genome organization but caution against assuming causal roles for the epigenome and 3D genome in gene regulation and function in ESCs.
当胚胎干细胞 (ESCs) 通过在两种小分子抑制剂 (2i) 中培养而被引导到原始多能性的基础状态时,会发生 DNA 去甲基化,导致多梳体(H3K27me3)从其靶位重新分布。在这里,我们证明 2i 中也会改变 3D 基因组组织,多梳靶位的染色质疏松,长距离多梳相互作用丧失。通过在向基础状态过渡期间防止 DNA 去甲基化,我们能够使 2i 中的 ESC 恢复 H3K27me3 分布,以及多梳体介导的、特征在于在血清中生长的原始 ESCs 的 3D 基因组组织。然而,这些细胞保留了 2i 基础状态 ESC 的功能特征。我们的研究结果表明 DNA 甲基化在塑造 3D 基因组组织的主要方面方面起着核心作用,但要谨慎对待在 ESC 中基因调控和功能的表观基因组和 3D 基因组的因果作用。