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Akt-Mediated Phosphorylation of EZH2 Suppresses Methylation of Lysine 27 in Histone H3

机译:AZH介导的EZH2磷酸化抑制组蛋白H3中赖氨酸27的甲基化

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摘要

Enhancer of Zeste homolog 2 (EZH2) is a methyltransferase that plays an important role in many biological processes through its ability to trimethylate lysine 27 in histone H3. Here, we show that Akt phosphorylates EZH2 at serine 21 and suppresses its methyltransferase activity by impeding EZH2 binding to histone H3, which results in a decrease of lysine 27 trimethylation and derepression of silenced genes. Our results imply that Akt regulates the methylation activity, through phosphorylation of EZH2, which may contribute to oncogenesis.
机译:Zeste同源物2(EZH2)的增强剂是一种甲基转移酶,通过其对组蛋白H3中的赖氨酸27进行三甲基化的能力,在许多生物学过程中均起着重要作用。在这里,我们显示Akt磷酸化EZH2在丝氨酸21,并通过阻止EZH2结合组蛋白H3抑制其甲基转移酶活性,这导致赖氨酸27三甲基化的减少和沉默基因的抑制。我们的结果表明,Akt通过EZH2的磷酸化调节甲基化活性,这可能有助于肿瘤发生。

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