1Department of Oncology, University of Western Ontario, Ontario, Canada.
Epigenetics Chromatin. 2009 Dec 2;2(1):18. doi: 10.1186/1756-8935-2-18.
In Saccharomyces cerevisiae genes that are located close to a telomere can become transcriptionally repressed by an epigenetic process known as telomere position effect. There is large variation in the level of the telomere position effect among telomeres, with many native ends exhibiting little repression.
Chromatin analysis, using microccocal nuclease and indirect end labelling, reveals distinct patterns for ends with different silencing states. Differences were observed in the promoter accessibility of a subtelomeric reporter gene and a characteristic array of phased nucleosomes was observed on the centromere proximal side of core X at a repressive end. The silent information regulator proteins 2 - 4, the yKu heterodimer and the subtelomeric core X element are all required for the maintenance of the chromatin structure of repressive ends. However, gene deletions of particular histone modification proteins can eliminate the silencing without the disruption of this chromatin structure.
Our data identifies chromatin features that correlate with the silencing state and indicate that an array of phased nucleosomes is not sufficient for full repression.
在酿酒酵母中,靠近端粒的基因可以通过一种称为端粒位置效应的表观遗传过程被转录抑制。端粒位置效应在端粒之间有很大的差异,许多天然端粒几乎没有抑制。
使用微球菌核酸酶和间接末端标记的染色质分析揭示了具有不同沉默状态的末端的不同模式。在一个亚端粒报告基因的启动子可及性和在一个有抑制性末端的核心 X 的着丝粒近端侧观察到特征性的相分期核小体阵列方面观察到差异。沉默信息调节蛋白 2-4、yKu 异二聚体和亚端粒核心 X 元件都需要维持抑制性末端的染色质结构。然而,特定组蛋白修饰蛋白的基因突变可以消除沉默,而不会破坏这种染色质结构。
我们的数据确定了与沉默状态相关的染色质特征,并表明相分期核小体阵列不足以完全抑制。