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本文引用的文献

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Expression-state boundaries in the mating-type region of fission yeast.裂殖酵母交配型区域中的表达状态边界。
Genetics. 2002 Jun;161(2):611-22. doi: 10.1093/genetics/161.2.611.
2
Heterochromatin: new possibilities for the inheritance of structure.异染色质:结构遗传的新可能性。
Curr Opin Genet Dev. 2002 Apr;12(2):178-87. doi: 10.1016/s0959-437x(02)00284-8.
3
Functional divergence between histone deacetylases in fission yeast by distinct cellular localization and in vivo specificity.裂殖酵母中组蛋白去乙酰化酶通过不同的细胞定位和体内特异性产生的功能差异
Mol Cell Biol. 2002 Apr;22(7):2170-81. doi: 10.1128/MCB.22.7.2170-2181.2002.
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The genome sequence of Schizosaccharomyces pombe.粟酒裂殖酵母的基因组序列。
Nature. 2002 Feb 21;415(6874):871-80. doi: 10.1038/nature724.
5
CDD: a database of conserved domain alignments with links to domain three-dimensional structure.CDD:一个保守结构域比对数据库,带有与结构域三维结构的链接。
Nucleic Acids Res. 2002 Jan 1;30(1):281-3. doi: 10.1093/nar/30.1.281.
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The fission yeast ES2 homologue, Bis1, interacts with the Ish1 stress-responsive nuclear envelope protein.裂殖酵母ES2同源物Bis1与Ish1应激反应性核膜蛋白相互作用。
J Biol Chem. 2002 Mar 22;277(12):10562-72. doi: 10.1074/jbc.M110686200. Epub 2001 Dec 20.
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Transitions in distinct histone H3 methylation patterns at the heterochromatin domain boundaries.异染色质结构域边界处不同组蛋白H3甲基化模式的转变。
Science. 2001 Aug 10;293(5532):1150-5. doi: 10.1126/science.1064150.
8
Rb targets histone H3 methylation and HP1 to promoters.视网膜母细胞瘤蛋白(Rb)将组蛋白H3甲基化和异染色质蛋白1(HP1)靶向至启动子区域。
Nature. 2001 Aug 2;412(6846):561-5. doi: 10.1038/35087620.
9
Role of histone H3 lysine 9 methylation in epigenetic control of heterochromatin assembly.组蛋白H3赖氨酸9甲基化在异染色质组装表观遗传调控中的作用。
Science. 2001 Apr 6;292(5514):110-3. doi: 10.1126/science.1060118. Epub 2001 Mar 15.
10
JmjC: cupin metalloenzyme-like domains in jumonji, hairless and phospholipase A2beta.JmjC:珠蛋白金属酶样结构域,存在于Jumonji、无毛蛋白和磷脂酶A2β中。
Trends Biochem Sci. 2001 Jan;26(1):7-9. doi: 10.1016/s0968-0004(00)01700-x.

一种新型的JmjC结构域蛋白调控裂殖酵母中的异染色质化。

A novel jmjC domain protein modulates heterochromatization in fission yeast.

作者信息

Ayoub Nabieh, Noma Ken-ichi, Isaac Sara, Kahan Tamar, Grewal Shiv I S, Cohen Amikam

机构信息

Department of Molecular Biology, The Hebrew University-Hadassah Medical School, Jerusalem, Israel 91010.

出版信息

Mol Cell Biol. 2003 Jun;23(12):4356-70. doi: 10.1128/MCB.23.12.4356-4370.2003.

DOI:10.1128/MCB.23.12.4356-4370.2003
PMID:12773576
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC156127/
Abstract

The heterochromatin domain at the mat locus of Schizosaccharomyces pombe is bounded by the IR-L and IR-R barriers. A genetic screen for mutations that promote silencing beyond IR-L revealed a novel gene named epe1, encoding a conserved nuclear protein with a jmjC domain. Disruption of epe1 promotes continuous spreading of heterochromatin-associated histone modifications and Swi6 binding to chromatin across heterochromatic barriers. It also enhances position effect variegation at heterochromatic domains, suppresses mutations in silencing genes, and stabilizes the repressed epigenetic state at the mat locus. However, it does not enhance silencing establishment. Our analysis suggests that the jmjC domain is essential for Epe1 activity and that Epe1 counteracts transcriptional silencing by negatively affecting heterochromatin stability. Consistent with this proposition, the meiotic stability of established heterochromatin beyond IR-L is diminished by Epe1 activity, and overexpression of Epe1 disrupts heterochromatin through acetylation of H3-K9 and H3-K14 and methylation of H3-K4. Furthermore, overexpression of Epe1 elevates the rate of chromosome loss. We propose that Epe1 helps control chromatin organization by down-regulating the stability of epigenetic marks that govern heterochromatization.

摘要

粟酒裂殖酵母交配型位点处的异染色质结构域由IR-L和IR-R边界限定。一项针对促进IR-L以外区域沉默的突变进行的遗传筛选,发现了一个名为epe1的新基因,它编码一种具有jmjC结构域的保守核蛋白。破坏epe1会促进异染色质相关组蛋白修饰的持续扩散,以及Swi6与跨越异染色质边界的染色质的结合。它还增强了异染色质区域的位置效应斑驳,抑制沉默基因中的突变,并稳定了交配型位点处的抑制性表观遗传状态。然而,它并不会增强沉默的建立。我们的分析表明,jmjC结构域对Epe1的活性至关重要,并且Epe1通过负面影响异染色质稳定性来对抗转录沉默。与此观点一致,IR-L以外已建立的异染色质的减数分裂稳定性会因Epe1的活性而降低,并且Epe1的过表达会通过H3-K9和H3-K14的乙酰化以及H3-K4的甲基化来破坏异染色质。此外,Epe1的过表达会提高染色体丢失率。我们提出,Epe1通过下调控制异染色质化的表观遗传标记的稳定性来帮助控制染色质组织。