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A Role for Nucleoporin Nup211 in Centromere Structure and Function in Schizosaccharomyces pombe.

机译:Nucleoporin Nup211在粟酒裂殖酵母的着丝粒结构和功能中的作用。

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摘要

Eukaryotic centromeres are the region upon which kinetochores assemble, directing attachment of spindle microtubules and faithful segregation of chromosomes during mitosis and meiosis. Except for a transient disruption in mitosis when chromosomes are segregated, centromeres of fission yeast Schizosaccharomyces pombe remain closely associated with the nuclear periphery. Similar to multicellular eukaryotic centromeres, they also maintain unique chromatin architecture, with a central core defined by the presence of the conserved centromeric histone H3 variant CENP-A, designated Cnp1 in S. pombe , that is flanked by histone H3 containing heterochromatin. While much progress has been made in understanding chromatin-associated factors important for proper centromere function, many questions remain.;In order to gain a better understanding of the factors involved in centromeric chromatin structure, we affinity purified and defined by mass spectrometry interactions among select proteins that had been implicated in proper Cnp1 localization and centromere function. These biochemical purifications revealed several proteins that may be involved in Cnp1 localization.;Purification and analyses of Cnp1 also led us to the identification of the Mlp1/Tpr nucleoporin homolog Nup211. We have found that Nup211 interacts with components of the inner nuclear basket of the nuclear pore, and co-purifies with centromeric chromatin proteins. Cells lacking Nup211 have substantial chromosome segregation defects, as observed by synthetic growth assay, flow cytometric analysis, and fluorescent microscopy. A series of immunoprecipitation experiments have revealed that Nup211 associates with centromeric DNA, and that, surprisingly, cells lacking Nup211 have increased histone H3 lysine 9 methylation, a marker of heterochromatin, and a reduction in Cnp1 levels at the central core. Moreover, cells lacking Nup211 have decreased transcription at centromeric loci, disruption of the stereotypical nucleosome structure found at the central core of S. pombe, and show striking changes in the distribution of heterochromatic foci in the nucleus.;By demonstrating that Nup211 is essential for the maintenance of normal central core chromatin state, these studies have shed light on a novel role for Nup211 in proper centromere structure and function in S. pombe , and suggest that Nup211 may play a role in preventing the invasion of flanking pericentric heterochromatin into the central core of centromeres.
机译:真核着丝粒是动植物集合的区域,指导纺锤体微管的附着和有丝分裂和减数分裂过程中染色体的忠实分离。除了当染色体分离时有丝分裂的短暂破坏,裂殖酵母粟酒裂殖酵母的着丝粒仍与核外围紧密相关。类似于多细胞真核着丝粒,它们还保持独特的染色质结构,其中心核心由守恒的着丝粒组蛋白H3变体CENP-A(在粟酒裂殖酵母中命名为Cnp1)的存在所定义,其侧翼是含有异染色质的组蛋白H3。尽管在了解对于正常着丝粒功能重要的染色质相关因子方面已取得了很大进展,但仍然存在许多问题。;为了更好地理解与着丝粒染色质结构有关的因子,我们通过质谱联用技术对亲和力进行了纯化和定义,与正常Cnp1定位和着丝粒功能有关的蛋白质。这些生化纯化揭示了可能与Cnp1定位有关的几种蛋白质。Cnp1的纯化和分析也使我们鉴定了Mlp1 / Tpr核孔蛋白同系物Nup211。我们发现Nup211与核孔内部核篮的成分相互作用,并与着丝粒染色质蛋白共纯化。缺乏Nup211的细胞具有大量染色体分离缺陷,如通过合成生长测定,流式细胞术分析和荧光显微镜观察到的。一系列免疫沉淀实验表明,Nup211与着丝粒DNA缔合,令人惊讶的是,缺少Nup211的细胞增加了组蛋白H3赖氨酸9甲基化,是异染色质的标记,并且中心核心的Cnp1水平降低。此外,缺乏Nup211的细胞在着丝粒基因座处的转录降低,在粟酒裂殖酵母中央核上发现的定型核小体结构破裂,并在核中异色病灶的分布中发生了惊人的变化。为了维持正常的中心核心染色质状态,这些研究为Nup211在粟酒裂殖酵母适当的着丝粒结构和功能中发挥了新的作用,并暗示Nup211可能在防止侧翼周围的异染色质侵入中央的过程中发挥了作用。着丝粒的核心。

著录项

  • 作者

    Morris, Corey Allen.;

  • 作者单位

    Harvard University.;

  • 授予单位 Harvard University.;
  • 学科 Biology Genetics.;Biology Cell.;Chemistry Biochemistry.
  • 学位 Ph.D.
  • 年度 2012
  • 页码 205 p.
  • 总页数 205
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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