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Methylation of the Arginine 2 in Histone H3 Controls Deposition of Lysine 4 Tri-Methylation

机译:组蛋白H3中精氨酸2的甲基化控制赖氨酸4 Tri-甲基化的沉积

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In a recent study, Kirmizis et al. demonstrated that H3R2 is methylated not only in mammals but also in Saccharomyces cerevisiae. By using a specific H3R2me2a antibody in a ChIP-on-Chip analysis the authors determined the distribution of the methylation throughout the yeast genome, finding an enrichment of H3R2me2a at all heterochromatic genes, at inactive euchromatic genes, and at the 3'-end of moderately transcribed genes.The presence of H3R2 methylation inversely correlates with the presence of H3K4 tri-methylation (H3K4me3) in all cases, reflecting the fact that H3R2 methylation disrupts the ability of the Set1- complex to methylate H3K4 by preventing the Set1-methyltransferase subunit Sppl from binding to to histone H3. These results show that H3R2 methylation controls the distribution of H3K4me3 and provide the first mechanistic insight into the function of arginine methylation on chromatin.
机译:在最近的研究中,Kirmizis等人。证明H3R2不仅在哺乳动物中而且在酿酒酵母中都被甲基化。通过在芯片上芯片分析中使用特定的H3R2me2a抗体,作者确定了甲基化在整个酵母基因组中的分布,发现所有杂色基因,无活性常染色体和3'-末端的H3R2me2a富集在所有情况下,H3R2甲基化的存在与H3K4三甲基化(H3K4me3)的存在成反比,反映出H3R2甲基化通过阻止Set1-甲基转移酶亚基破坏了Set1-复合物甲基化H3K4的能力这一事实。 Sppl从绑定到组蛋白H3。这些结果表明,H3R2甲基化控制H3K4me3的分布,并为精氨酸甲基化在染色质上的功能提供了第一个机理见解。

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