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Analysis of human histone H2AZ deposition in vivo argues against its direct role in epigenetic templating mechanisms.对人类组蛋白H2AZ在体内沉积的分析表明,它在表观遗传模板机制中不发挥直接作用。
Mol Cell Biol. 2006 Jul;26(14):5325-35. doi: 10.1128/MCB.00584-06.
2
Epigenetic regulators and histone modification.表观遗传调控因子与组蛋白修饰
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3
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BORIS/CTCFL epigenetically reprograms clustered CTCF binding sites into alternative transcriptional start sites.BORIS/CTCFL 通过表观遗传重编程将聚集的 CTCF 结合位点转化为替代的转录起始位点。
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本文引用的文献

1
How is epigenetic information on chromatin inherited after DNA replication?染色质上的表观遗传信息在DNA复制后是如何遗传的?
Ernst Schering Res Found Workshop. 2006(57):89-96. doi: 10.1007/3-540-37633-x_5.
2
Preferential occupancy of histone variant H2AZ at inactive promoters influences local histone modifications and chromatin remodeling.组蛋白变体H2AZ在无活性启动子上的优先占据会影响局部组蛋白修饰和染色质重塑。
Proc Natl Acad Sci U S A. 2005 Dec 20;102(51):18385-90. doi: 10.1073/pnas.0507975102. Epub 2005 Dec 12.
3
Variant histone H2A.Z is globally localized to the promoters of inactive yeast genes and regulates nucleosome positioning.变体组蛋白H2A.Z在全基因组范围内定位于无活性酵母基因的启动子区域,并调控核小体定位。
PLoS Biol. 2005 Dec;3(12):e384. doi: 10.1371/journal.pbio.0030384. Epub 2005 Nov 1.
4
Histone variant H2A.Z marks the 5' ends of both active and inactive genes in euchromatin.组蛋白变体H2A.Z标记常染色质中活跃基因和非活跃基因的5'端。
Cell. 2005 Oct 21;123(2):233-48. doi: 10.1016/j.cell.2005.10.002.
5
Genome-wide dynamics of Htz1, a histone H2A variant that poises repressed/basal promoters for activation through histone loss.Htz1的全基因组动态变化,Htz1是一种组蛋白H2A变体,通过组蛋白缺失使抑制/基础启动子为激活做好准备。
Cell. 2005 Oct 21;123(2):219-31. doi: 10.1016/j.cell.2005.08.036.
6
Histone variants meet their match.组蛋白变体棋逢对手。
Nat Rev Mol Cell Biol. 2005 Feb;6(2):139-49. doi: 10.1038/nrm1567.
7
H2A.Z alters the nucleosome surface to promote HP1alpha-mediated chromatin fiber folding.H2A.Z改变核小体表面以促进HP1α介导的染色质纤维折叠。
Mol Cell. 2004 Nov 19;16(4):655-61. doi: 10.1016/j.molcel.2004.10.023.
8
The role of histones in chromatin remodelling during mammalian spermiogenesis.组蛋白在哺乳动物精子发生过程中染色质重塑中的作用。
Eur J Biochem. 2004 Sep;271(17):3459-69. doi: 10.1111/j.1432-1033.2004.04266.x.
9
SWRred not shaken; mixing the histones.SWRred未被摇动;混合组蛋白。
Cell. 2004 Apr 2;117(1):5-7. doi: 10.1016/s0092-8674(04)00296-x.
10
Histone H3.3 is enriched in covalent modifications associated with active chromatin.组蛋白H3.3富含与活性染色质相关的共价修饰。
Proc Natl Acad Sci U S A. 2004 Feb 10;101(6):1525-30. doi: 10.1073/pnas.0308092100. Epub 2004 Jan 19.

对人类组蛋白H2AZ在体内沉积的分析表明,它在表观遗传模板机制中不发挥直接作用。

Analysis of human histone H2AZ deposition in vivo argues against its direct role in epigenetic templating mechanisms.

作者信息

Viens Antoine, Mechold Undine, Brouillard Franck, Gilbert Cristele, Leclerc Philippe, Ogryzko Vasily

机构信息

CNRS UMR 8126, Institut Gustave-Roussy, PR1, 39 rue Camille Desmoulin, 94100 Villejuif, France.

出版信息

Mol Cell Biol. 2006 Jul;26(14):5325-35. doi: 10.1128/MCB.00584-06.

DOI:10.1128/MCB.00584-06
PMID:16809769
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1592707/
Abstract

Chromatin is considered to be a principal carrier of epigenetic information due to the ability of alternative chromatin states to persist through generations of cell divisions and to spread on DNA. Replacement histone variants are novel candidates for epigenetic marking of chromatin. We developed a novel approach to analyze the chromatin environment of nucleosomes containing a particular replacement histone. We applied it to human H2AZ, one of the most studied alternative histones. We find that neither H2AZ itself nor other features of the H2AZ-containing nucleosome spread to the neighboring nucleosomes in vivo, arguing against a role for H2AZ as a self-perpetuating epigenetic mark.

摘要

由于染色质的不同状态能够在细胞分裂的世代中持续存在并在DNA上扩散,因此染色质被认为是表观遗传信息的主要载体。替换组蛋白变体是染色质表观遗传标记的新候选者。我们开发了一种新方法来分析含有特定替换组蛋白的核小体的染色质环境。我们将其应用于人类H2AZ,这是研究最多的替代组蛋白之一。我们发现,无论是H2AZ本身还是含H2AZ的核小体的其他特征,在体内都不会扩散到相邻的核小体,这表明H2AZ不具有作为自我延续的表观遗传标记的作用。