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Condensin targets and reduces unwound DNA structures associated with transcription in mitotic chromosome condensation

机译:凝缩蛋白靶向并减少与有丝分裂染色体凝缩中转录相关的解链DNA结构

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摘要

Chromosome condensation is a hallmark of mitosis in eukaryotes and is a prerequisite for faithful segregation of genetic material to daughter cells. Here we show that condensin, which is essential for assembling condensed chromosomes, helps to preclude the detrimental effects of gene transcription on mitotic condensation. ChIP-seq profiling reveals that the fission yeast condensin preferentially binds to active protein-coding genes in a transcription-dependent manner during mitosis. Pharmacological and genetic attenuation of transcription largely rescue bulk chromosome segregation defects observed in condensin mutants. We also demonstrate that condensin is associated with and reduces unwound DNA segments generated by transcription, providing a direct link between an in vitro activity of condensin and its in vivo function. The human condensin isoform condensin I also binds to unwound DNA regions at the transcription start sites of active genes, implying that our findings uncover a fundamental feature of condensin complexes.
机译:染色体凝结是真核生物中有丝分裂的标志,也是将遗传物质忠实分离到子代细胞的先决条件。在这里,我们显示凝聚素(组装凝聚染色体必不可少的)有助于排除基因转录对有丝分裂凝聚的有害影响。 ChIP-seq分析显示,裂变酵母凝缩蛋白在有丝分裂过程中优先以转录依赖性方式与活性蛋白编码基因结合。转录的药理和遗传减毒很大程度上可以挽救在凝聚素突变体中观察到的大量染色体分离缺陷。我们还证明了凝缩蛋白与转录产生的未缠绕DNA片段相关并减少了其解链,提供了凝缩蛋白的体外活性与其体内功能之间的直接联系。人凝缩蛋白同工型凝缩蛋白I还与活性基因转录起始位点的未缠绕DNA区域结合,这表明我们的发现揭示了凝缩蛋白复合物的基本特征。

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