Laboratory of Cell Genetics (CEGE), Department of Biology, Vrije Universiteit Brussel (VUB), Brussels, Belgium.
Laboratory of Pathophysiological Cell Signaling (PACS), Department of Biology, Vrije Universiteit Brussel (VUB), Brussels, Belgium.
Dev Growth Differ. 2020 May;62(4):232-242. doi: 10.1111/dgd.12659. Epub 2020 Apr 22.
Polycomb group (PcG) RING finger protein 5 (PCGF5) is a core component of the so-called Polycomb repressive complex 1.5 (PRC1.5), which is involved in epigenetic transcriptional repression. To explore the developmental function of Pcgf5, we generated Pcgf5 knockout (Pcgf5 ) mouse embryonic stem cell (mESC) lines with the help of CRISPR/Cas9 technology. We subjected the Pcgf5 and wild-type (WT) mESCs to a differentiation protocol toward mesodermal-cardiac cell types as aggregated embryoid bodies (EBs) and we found that knockout of Pcgf5 delayed the generation of the three germ layers, especially the ectoderm. Further, disruption of Pcgf5 impacted the epithelial-mesenchymal transition during EB morphogenesis and differentially affected the gene expression of essential developmental signaling pathways such as Nodal and Wnt. Finally, we also unveiled that loss of Pcgf5 induced the repression of genes involved in the Notch pathway, which may explain the enhancement of cardiomyocyte maturation and the dampening of ectodermal-neural differentiation observed in the Pcgf5 EBs.
多梳抑制复合物 1.5(PRC1.5)的核心成分之一是多梳组蛋白(PcG)RING 指蛋白 5(PCGF5),它参与表观遗传转录抑制。为了探索 Pcgf5 的发育功能,我们利用 CRISPR/Cas9 技术生成了 Pcgf5 敲除(Pcgf5 )小鼠胚胎干细胞(mESC)系。我们将 Pcgf5 和野生型(WT)mESC 置于朝向中胚层-心脏细胞类型的分化方案中,作为聚集的胚状体(EBs),我们发现敲除 Pcgf5 延迟了三个胚层的生成,特别是外胚层。此外,Pcgf5 的破坏会影响 EB 形态发生过程中的上皮-间充质转化,并对 Nodal 和 Wnt 等重要发育信号通路的基因表达产生不同的影响。最后,我们还揭示了 Pcgf5 的缺失会诱导 Notch 通路相关基因的抑制,这可能解释了在 Pcgf5 EBs 中观察到的心肌细胞成熟增强和外胚层-神经分化减弱。