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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.

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。

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