Laboratory of Muscle Stem Cells and Gene Regulation, National Institute of Arthritis, Musculoskeletal and Skin Diseases, National Institutes of Health, Bethesda, MD 20852, USA.
Mol Cell. 2012 Jan 27;45(2):255-62. doi: 10.1016/j.molcel.2011.11.019. Epub 2011 Dec 22.
Polycomb group (PcG) proteins initiate the formation of repressed chromatin domains and regulate developmental gene expression. A mammalian PcG protein, enhancer of zeste homolog 2 (Ezh2), triggers transcriptional repression by catalyzing the addition of methyl groups onto lysine 27 of histone H3 (H3K27me2/3). This action facilitates the binding of other PcG proteins to chromatin for purposes of transcriptional silencing. Interestingly, there exists a paralog of Ezh2, termed Ezh1, whose primary function remains unclear. Here, we provide evidence for genome-wide association of Ezh1 complex with active epigenetic mark (H3K4me3), RNA polymerase II (Pol II), and mRNA production. Ezh1 depletion reduced global Pol II occupancy within gene bodies and resulted in delayed transcriptional activation during differentiation of skeletal muscle cells. Conversely, overexpression of wild-type Ezh1 led to premature gene activation and rescued Pol II occupancy defects in Ezh1-depleted cells. Collectively, these findings reveal a role for a PcG complex in promoting mRNA transcription.
多梳抑制复合物(PcG)蛋白启动抑制性染色质结构域的形成,并调节发育相关基因的表达。一种哺乳动物 PcG 蛋白,EZH2(enhancer of zeste homolog 2),通过催化组蛋白 H3 赖氨酸 27(H3K27me2/3)上的甲基化来触发转录抑制。该作用促进了其他 PcG 蛋白与染色质的结合,从而实现转录沉默。有趣的是,存在 Ezh2 的一个旁系同源物,称为 Ezh1,但其主要功能仍不清楚。在这里,我们提供了 Ezh1 复合物与活性表观遗传标记(H3K4me3)、RNA 聚合酶 II(Pol II)和 mRNA 产生的全基因组关联的证据。Ezh1 缺失减少了基因体内的全局 Pol II 占据,导致在骨骼肌细胞分化过程中转录激活延迟。相反,野生型 Ezh1 的过表达导致基因过早激活,并挽救了 Ezh1 缺失细胞中 Pol II 占据的缺陷。总之,这些发现揭示了 PcG 复合物在促进 mRNA 转录中的作用。