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Topoisomerase II binds nucleosome-free DNA and acts redundantly with topoisomerase I to enhance recruitment of RNA Pol II in budding yeast

机译:拓扑异构酶II结合无核小体的DNA,并与拓扑异构酶I冗余发挥作用,以增强发芽酵母中RNA Pol II的募集

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摘要

DNA topoisomerases are believed to promote transcription by removing excessive DNA supercoils produced during elongation. However, it is unclear how topoisomerases in eukaryotes are recruited and function in the transcription pathway in the context of nucleosomes. To address this problem we present high-resolution genome-wide maps of one of the major eukaryotic topoisomerases, Topoisomerase II (Top2) and nucleosomes in the budding yeast, Saccharomyces cerevisiae. Our data indicate that at promoters Top2 binds primarily to DNA that is nucleosome-free. However, although nucleosome loss enables Top2 occupancy, the opposite is not the case and the loss of Top2 has little effect on nucleosome density. We also find that Top2 is involved in transcription. Not only is Top2 enriched at highly transcribed genes, but Top2 is required redundantly with Topi for optimal recruitment of RNA polymerase II at their promoters. These findings and the examination of candidate-activated genes suggest that nucleosome loss induced by nucleosome remodeling factors during gene activation enables Top2 binding, which in turn acts redundantly with Topi to enhance recruitment of RNA polymerase II.
机译:据信DNA拓扑异构酶可通过去除延伸过程中产生的过量DNA超螺旋来促进转录。然而,目前尚不清楚真核生物中拓扑异构酶如何在核小体的背景下被募集并在转录途径中发挥作用。为了解决这个问题,我们提出了一种主要的真核拓扑异构酶,拓扑异构酶II(Top2)和出芽的酵母,酿酒酵母中的核小体的高分辨率全基因组图。我们的数据表明,在启动子上,Top2主要与无核小体的DNA结合。然而,尽管核小体丢失使Top2占据,但情况并非如此,并且Top2的丢失对核小体密度几乎没有影响。我们还发现Top2参与转录。 Top2不仅在高度转录的基因中富集,而且Top2也是多余的,因为Topi才能在其启动子处最佳募集RNA聚合酶II。这些发现和对候选激活基因的检查表明,在基因激活过程中,由核小体重塑因子诱导的核小体丢失使Top2结合成为可能,而Top2结合又与Topi多余,从而增强了RNA聚合酶II的募集。

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  • 作者单位

    Department of Biological Chemistry, David Geffen School of Medicine, and the Molecular Biology Institute, University of California, Los Angeles,CA 90095;

    Agilent Technologies, 5301 Steven Creek Boulevard, Santa Clara,CA 95051;

    Department of Biological Chemistry, David Geffen School of Medicine, and the Molecular Biology Institute, University of California, Los Angeles,CA 90095;

    Department of Biological Chemistry, David Geffen School of Medicine, and the Molecular Biology Institute, University of California, Los Angeles,CA 90095;

  • 收录信息 美国《科学引文索引》(SCI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    histone eviction; relaxase; gene regulation;

    机译:组蛋白逐出;松弛酶;基因调控;

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