Graduate School of Engineering, The University of Tokyo, Tokyo 113-0033, Japan.
Graduate School of Engineering, The University of Tokyo, Tokyo 113-0033, Japan.
Curr Opin Neurobiol. 2019 Dec;59:164-173. doi: 10.1016/j.conb.2019.07.003. Epub 2019 Aug 6.
While all the developmental genes are temporarily repressed for future activation in the pluripotent stem cells, non-neural genes become persistently repressed in the course of commitment to the neuronal lineage. Although Polycomb group proteins (PcG) are key factors for both temporary and persistent repression of the developmental genes, how the same group of proteins can differentially repress target genes remains unclarified. The identification of a variety of PcG complexes and activities sheds light on these issues. In this review, based on the recent findings including those with the use of interactome and Chromosome Conformation Capture (3C)-type analyses, we summarize the molecular mechanisms of PcG-mediated gene regulation and discuss how PcG regulates cell fate specification during neural development.
虽然所有的发育基因在多能干细胞中都被暂时抑制,以便将来激活,但在向神经元谱系分化的过程中,非神经基因会持续被抑制。尽管 Polycomb 组蛋白 (PcG) 是暂时和持续抑制发育基因的关键因素,但同一组蛋白如何能差异地抑制靶基因尚不清楚。多种 PcG 复合物和活性的鉴定为这些问题提供了线索。在这篇综述中,我们基于最近的发现,包括使用互作组和染色质构象捕获(3C)分析的发现,总结了 PcG 介导的基因调控的分子机制,并讨论了 PcG 如何在神经发育过程中调节细胞命运特化。