生物
PRC2
甲基化
细胞生物学
细胞分化
DNA甲基化
EZH2型
遗传学
DNA
基因表达
基因
作者
Serena Sanulli,N. Justin,Aurélie Teissandier,Katia Ancelin,Manuela Portoso,Matthieu Caron,Audrey Michaud,Bérangère Lombard,Simão Teixeira da Rocha,John Offer,Damarys Loew,Nicolas Servant,Michel Wassef,Fabienne Burlina,S.J. Gamblin,Édith Heard,Raphaël Margueron
出处
期刊:Molecular Cell
[Elsevier BV]
日期:2015-01-22
卷期号:57 (5): 769-783
被引量:278
标识
DOI:10.1016/j.molcel.2014.12.020
摘要
Polycomb Group (PcG) proteins maintain transcriptional repression throughout development, mostly by regulating chromatin structure. Polycomb Repressive Complex 2 (PRC2), a component of the Polycomb machinery, is responsible for the methylation of histone H3 lysine 27 (H3K27me2/3). Jarid2 was previously identified as a cofactor of PRC2, regulating PRC2 targeting to chromatin and its enzymatic activity. Deletion of Jarid2 leads to impaired orchestration of gene expression during cell lineage commitment. Here, we reveal an unexpected crosstalk between Jarid2 and PRC2, with Jarid2 being methylated by PRC2. This modification is recognized by the Eed core component of PRC2 and triggers an allosteric activation of PRC2's enzymatic activity. We show that Jarid2 methylation is important to promote PRC2 activity at a locus devoid of H3K27me3 and for the correct deposition of this mark during cell differentiation. Our results uncover a regulation loop where Jarid2 methylation fine-tunes PRC2 activity depending on the chromatin context.
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