PRC2
生物
心理压抑
多组蛋白
组蛋白
细胞生物学
胚胎干细胞
泛素
遗传学
组蛋白H3
抑制因子
基因
基因表达
作者
Simone Tamburri,Elisa Lavarone,Daniel Fernández-Pérez,Eric Conway,Marika Zanotti,Daria Manganaro,Diego Pasini
出处
期刊:Molecular Cell
[Elsevier BV]
日期:2019-12-26
卷期号:77 (4): 840-856.e5
被引量:299
标识
DOI:10.1016/j.molcel.2019.11.021
摘要
Polycomb group proteins (PcGs) maintain transcriptional repression to preserve cellular identity in two distinct repressive complexes, PRC1 and PRC2, that modify histones by depositing H2AK119ub1 and H3K27me3, respectively. PRC1 and PRC2 exist in different variants and show a complex regulatory cross-talk. However, the contribution that H2AK119ub1 plays in mediating PcG repressive functions remains largely controversial. Using a fully catalytic inactive RING1B mutant, we demonstrated that H2AK119ub1 deposition is essential to maintain PcG-target gene repression in embryonic stem cells (ESCs). Loss of H2AK119ub1 induced a rapid displacement of PRC2 activity and a loss of H3K27me3 deposition. This preferentially affected PRC2.2 variant with respect to PRC2.1, destabilizing canonical PRC1 activity. Finally, we found that variant PRC1 forms can sense H2AK119ub1 deposition, which contributes to their stabilization specifically at sites where this modification is highly enriched. Overall, our data place H2AK119ub1 deposition as a central hub that mounts PcG repressive machineries to preserve cell transcriptional identity.
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