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Epigenetic countermarks in mitotic chromosome condensation

机译:有丝分裂染色体浓缩中的表观遗传标记

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Mitosis in metazoans is characterized by abundant phosphorylation of histone H3 and involves the recruitment of condensin complexes to chromatin. The relationship between the 2 phenomena and their respective contributions to chromosome condensation in vivo remain poorly understood. Recent studies have shown that H3T3 phosphorylation decreases binding of histone readers to methylated H3K4 in vitro and is essential to displace the corresponding proteins from mitotic chromatin in vivo. Together with previous observations, these data provide further evidence for a role of mitotic histone H3 phosphorylation in blocking transcriptional programs or preserving the ‘memory’ PTMs. Mitotic protein exclusion can also have a role in depopulating the chromatin template for subsequent condensin loading. H3 phosphorylation thus serves as an integral step in the condensation of chromosome arms.
机译:后生动物的有丝分裂的特征在于组蛋白H3的大量磷酸化,并涉及凝聚素复合物向染色质的募集。两种现象之间的关系及其各自对体内染色体浓缩的贡献仍知之甚少。最近的研究表明,H3T3磷酸化可在体外降低组蛋白阅读器与甲基化H3K4的结合,对于在体内从有丝分裂染色质置换相应的蛋白质至关重要。这些数据与以前的观察结果一起,为有丝分裂组蛋白H3磷酸化在阻止转录程序或保留“记忆” PTM中的作用提供了进一步的证据。有丝分裂蛋白的排除也可能在减少染色质模板以供随后的凝集素加载中起作用。因此,H3磷酸化是染色体臂缩合中不可或缺的步骤。

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