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首页> 外文期刊>Proceedings of the National Academy of Sciences of the United States of America >Nucleosome depletion at yeast terminators is not intrinsic and can occur by a transcriptional mechanism linked to 3'-end formation
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Nucleosome depletion at yeast terminators is not intrinsic and can occur by a transcriptional mechanism linked to 3'-end formation

机译:酵母终止子上的核小体耗竭不是固有的,可以通过与3'端形成相关的转录机制发生

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摘要

Genome-wide mapping of nucleosomes generated by micrococcal nuclease (MNase) suggests that yeast promoter and terminator re-gions are very depleted of nucleosomes, predominantly because their DNA sequences intrinsically disfavor nucleosome formation. However, MNase has strong DNA sequence specificity that favors cleavage at promoters and terminators and accounts for some of the correlation between occupancy patterns of nucleosomes assembled in vivo and in vitro. Using an improved method for measuring nucleosome occupancy in vivo that does not involve MNase, we confirm that promoter regions are strongly depleted of nucleosomes, but find that terminator regions are much less depleted than expected. Unlike at promoter regions, nucleosome occupancy at terminators is strongly correlated with the orienta-tion of and distance to adjacent genes. In addition, nucleosome occupancy at terminators is strongly affected by growth condi-tions, indicating that it is not primarily determined by intrinsic histone-DNA interactions. Rapid removal of RNA polymerase II (pol II) causes increased nucleosome occupancy at terminators, strongly suggesting a transcription-based mechanism of nucleo-some depletion. However, the distinct behavior of terminator regions and their corresponding coding regions suggests that nucleosome depletion at terminators is not simply associated with passage of pol II, but rather involves a distinct mechanism linked to 3'-end formation.
机译:微球菌核酸酶(MNase)产生的核小体的全基因组图谱表明,酵母启动子和终止子区域中的核小体非常少,主要是因为它们的DNA序列本质上不利于核小体的形成。然而,MNase具有很强的DNA序列特异性,有利于在启动子和终止子处裂解,并解释了体内和体外组装的核小体的占据模式之间的一些相关性。使用一种不涉及MNase的用于测量体内核小体占用率的改进方法,我们确认启动子区域的核小体强烈消耗,但发现终止子区域的耗竭远少于预期。与启动子区域不同,终止子处的核小体占用与相邻基因的方向和与该基因的距离密切相关。另外,终止条件下核小体的占有率受生长条件的强烈影响,这表明它不是主要由内在组蛋白-DNA相互作用决定的。快速去除RNA聚合酶II(pol II)会导致终止子上核小体的占据增加,这强烈暗示了核小体耗竭的基于转录的机制。然而,终止子区域及其相应的编码区的独特行为表明,终止子上核小体的消耗不仅与pol II的通过有关,而且还涉及与3'端形成相关的独特机制。

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  • 作者单位

    Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, MA 02115;

    rnDepartment of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, MA 02115;

    rnDepartment of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, MA 02115;

    rnDepartment of Biostatistics and Computational Biology, Dana Farber Cancer Institute, Boston, MA 02115 School of Life Sciences and Technology, Tongji University, Shanghai 200092, People's Republic of China;

    rnDepartment of Biostatistics and Computational Biology, Dana Farber Cancer Institute, Boston, MA 02115;

    rnDepartment of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, MA 02115;

  • 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

    nucleosome positioning; chromatin structure; genome organization;

    机译:核小体定位;染色质结构基因组组织;

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