Center for Molecular Medicine Cologne (CMMC), University of Cologne, Germany.
Department II of Internal Medicine, University Hospital Cologne, Germany.
Brief Funct Genomics. 2019 Nov 19;18(6):358-366. doi: 10.1093/bfgp/elz022.
Polycomb group proteins (PcGs) control the epigenetic and transcriptional state of developmental genes and regulatory elements during mammalian embryogenesis. Moreover, PcGs can also contribute to 3D genome organization, adding an additional layer of complexity to their regulatory functions. Understanding the mechanistic basis and the dynamics of PcG-dependent chromatin structures will help us untangle the full complexity of PcG function during development. Since most studies concerning the 3D organization of PcG-bound chromatin in mammals have been performed in embryonic stem cells (ESCs), here we will focus on this cell type characterized by its unique self-renewal and pluripotency properties. More specifically, we will highlight recent findings and discuss open questions regarding how PcG-dependent changes in 3D chromatin architecture control gene expression, cellular identity and differentiation potential in ESCs. We believe that this can serve to illustrate the diverse regulatory mechanisms by which PcG proteins control the proper execution of gene expression programs during mammalian embryogenesis.
多梳蛋白组(PcG)蛋白在哺乳动物胚胎发生过程中控制发育基因和调控元件的表观遗传和转录状态。此外,PcG 还可以促进 3D 基因组组织,为其调控功能增加了一个额外的复杂性层次。了解 PcG 依赖性染色质结构的机制基础和动态将有助于我们解开 PcG 在发育过程中的全部功能的复杂性。由于大多数关于哺乳动物中 PcG 结合染色质的 3D 组织的研究都是在胚胎干细胞(ESC)中进行的,因此我们将在这里重点介绍具有独特自我更新和多能性特性的这种细胞类型。更具体地说,我们将强调最近的发现,并讨论有关 PcG 依赖性 3D 染色质结构变化如何控制 ESC 中的基因表达、细胞身份和分化潜能的开放性问题。我们相信,这可以说明 PcG 蛋白在哺乳动物胚胎发生过程中控制基因表达程序的适当执行的多种调节机制。