PRC2
多组蛋白
组蛋白H3
生物
组蛋白甲基转移酶
组蛋白
EZH2型
Hox基因
基因表达调控
组蛋白H2A
甲基转移酶
基因
遗传学
基因表达
细胞生物学
甲基化
抑制因子
作者
Cyril S. Anyetei‐Anum,Mary Leatham‐Jensen,Geoffrey Fox,B. Rutledge Smith,Venkat R. Chirasani,Krzysztof Krajewski,Brian D. Strahl,Jill M. Dowen,A. Gregory Matera,Robert J. Duronio,Daniel J. McKay
标识
DOI:10.1101/gad.352181.124
摘要
Tight control over cell identity gene expression is necessary for proper adult form and function. The opposing activities of Polycomb and trithorax complexes determine the on/off state of cell identity genes such as the Hox factors. Polycomb group complexes repress target genes, whereas trithorax group complexes are required for their expression. Although trithorax and its orthologs function as methyltransferases specific to histone H3 lysine 4 (H3K4), there is no direct evidence that H3K4 regulates Polycomb group target genes in vivo. Using histone gene replacement in Drosophila , we provide evidence of two key roles for replication-dependent histone H3.2K4 in Polycomb target gene control. First, we found that H3.2K4 mutants mimic H3.2K4me3 in antagonizing methyltransferase activity of the PRC2 Polycomb group complex. Second, we found that H3.2K4 is also required for proper activation of Polycomb targets. We conclude that H3.2K4 directly regulates Polycomb target gene expression.
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