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本文引用的文献

1
Differential nuclear localization does not determine the silencing status of Saccharomyces cerevisiae telomeres.核定位差异并不能决定酿酒酵母端粒的沉默状态。
Genetics. 2007 Dec;177(4):2019-29. doi: 10.1534/genetics.107.079848.
2
Telomerase and Tel1p preferentially associate with short telomeres in S. cerevisiae.端粒酶和Tel1p在酿酒酵母中优先与短端粒结合。
Mol Cell. 2007 Aug 17;27(4):550-61. doi: 10.1016/j.molcel.2007.07.016. Epub 2007 Jul 26.
3
Genome-wide mapping of ORC and Mcm2p binding sites on tiling arrays and identification of essential ARS consensus sequences in S. cerevisiae.酿酒酵母中ORC和Mcm2p结合位点在平铺阵列上的全基因组图谱绘制以及必需ARS共有序列的鉴定。
BMC Genomics. 2006 Oct 26;7:276. doi: 10.1186/1471-2164-7-276.
4
Asymmetric positioning of nucleosomes and directional establishment of transcriptionally silent chromatin by Saccharomyces cerevisiae silencers.酿酒酵母沉默子对核小体的不对称定位及转录沉默染色质的定向建立
Mol Cell Biol. 2006 Oct;26(20):7806-19. doi: 10.1128/MCB.01197-06. Epub 2006 Aug 14.
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Telomeric silencing of an open reading frame in Saccharomyces cerevisiae.酿酒酵母中一个开放阅读框的端粒沉默
Genetics. 2006 Jun;173(2):1169-73. doi: 10.1534/genetics.106.058420. Epub 2006 Apr 2.
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Characterization of the grappa gene, the Drosophila histone H3 lysine 79 methyltransferase.格拉帕基因(果蝇组蛋白H3赖氨酸79甲基转移酶)的特性分析。
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Live imaging of telomeres: yKu and Sir proteins define redundant telomere-anchoring pathways in yeast.端粒的实时成像:yKu和Sir蛋白在酵母中定义了冗余的端粒锚定途径。
Curr Biol. 2002 Dec 23;12(24):2076-89. doi: 10.1016/s0960-9822(02)01338-6.
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Rap1-Sir4 binding independent of other Sir, yKu, or histone interactions initiates the assembly of telomeric heterochromatin in yeast.Rap1与Sir4的结合独立于其他Sir、yKu或组蛋白相互作用,启动了酵母端粒异染色质的组装。
Genes Dev. 2002 Jun 15;16(12):1528-39. doi: 10.1101/gad.988802.
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Genome-wide distribution of ORC and MCM proteins in S. cerevisiae: high-resolution mapping of replication origins.酿酒酵母中ORC和MCM蛋白的全基因组分布:复制起点的高分辨率图谱
Science. 2001 Dec 14;294(5550):2357-60. doi: 10.1126/science.1066101.
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Localization of yeast telomeres to the nuclear periphery is separable from transcriptional repression and telomere stability functions.酵母端粒定位于核周边与转录抑制和端粒稳定性功能可分离。
Mol Cell. 2001 Jul;8(1):189-99. doi: 10.1016/s1097-2765(01)00287-8.

亚端粒元件影响但不决定酿酒酵母端粒处的沉默水平。

Subtelomeric elements influence but do not determine silencing levels at Saccharomyces cerevisiae telomeres.

作者信息

Mondoux Michelle A, Zakian Virginia A

机构信息

Department of Molecular Biology, Princeton University, Princeton, New Jersey 08544, USA.

出版信息

Genetics. 2007 Dec;177(4):2541-6. doi: 10.1534/genetics.107.079806.

DOI:10.1534/genetics.107.079806
PMID:18073447
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2219501/
Abstract

In Saccharomyces cerevisiae, genes placed near telomeres are transcriptionally repressed (telomere position effect, TPE). Although telomeric DNA sequence is the same at all chromosome ends, the subtelomeric elements (STEs) and level of TPE vary from telomere to telomere. We tested whether STEs determine TPE levels. STEs contributed to TPE, as deleting the X element from the VI-R telomere modestly decreased silencing at this telomere. However, STEs were not the major determinant of TPE levels, as inserting the VI-R X element at the truncated VII-L telomere did not increase TPE. These data suggest that the TPE levels of individual telomeres are dependent on some aspect of chromosome context.

摘要

在酿酒酵母中,位于端粒附近的基因会受到转录抑制(端粒位置效应,TPE)。尽管所有染色体末端的端粒DNA序列相同,但亚端粒元件(STE)和TPE水平在不同端粒之间存在差异。我们测试了STE是否决定TPE水平。STE对TPE有贡献,因为从VI-R端粒删除X元件会适度降低该端粒处的沉默。然而,STE不是TPE水平的主要决定因素,因为在截短的VII-L端粒插入VI-R X元件并没有增加TPE。这些数据表明,单个端粒的TPE水平取决于染色体背景的某些方面。