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Polo kinase regulates mitotic chromosome condensation by hyperactivation of condensin DNA supercoiling activity.

机译:Polo激酶通过凝集素DNA超螺旋活性的过度激活来调节有丝分裂染色体的凝缩。

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摘要

A defining feature of mitosis is the reorganization of chromosomes into highly condensed structures capable of withstanding separation and large-scale intracellular movements. This reorganization is promoted by condensin, an evolutionarily conserved multisubunit ATPase. Here we show, using budding yeast, that condensin is regulated by phosphorylation specifically in anaphase. This phosphorylation depends on several mitotic regulators, and the ultimate effector is the Polo kinase Cdc5. We demonstrate that Cdc5 directly phosphorylates all three regulatory subunits of the condensin complex in vivo and that this causes a hyperactivation of condensin DNA supercoiling activity. Strikingly, abrogation of condensin phosphorylation is incompatible with viability, and cells expressing condensin mutants that have a reduced ability to be phosphorylated in vivo are defective in anaphase-specific chromosome condensation. Our results reveal the existence of a regulatory mechanism essential for the promotion of genome integrity through the stimulation of chromosome condensation in late mitosis.
机译:有丝分裂的定义特征是将染色体重组为能够承受分离和大规模细胞内运动的高度浓缩的结构。重组素dendensin是一种进化上保守的多亚基ATPase,可以促进这种重组。在这里,我们显示出使用发芽酵母,凝缩蛋白在后期特别受磷酸化调节。这种磷酸化取决于几种有丝分裂调节剂,最终的效应子是Polo激酶Cdc5。我们证明,Cdc5直接磷酸化凝集素复杂体内的所有三个调节亚基,并且这会导致凝缩蛋白DNA超螺旋活性的过度激活。令人惊讶的是,凝缩蛋白磷酸化的废除与生存力不相容,表达凝缩蛋白突变体的细胞在体内磷酸化能力降低的细胞在后期特异性染色体凝缩中是有缺陷的。我们的结果揭示了通过在晚期有丝分裂中刺激染色体凝结来促进基因组完整性必不可少的调控机制的存在。

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