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Suv39h-Dependent H3K9me3 Marks Intact Retrotransposons and Silences LINE Elements in Mouse Embryonic Stem Cells

机译:Suv39h依赖的H3K9me3标记完整的逆转座子和沉默小鼠胚胎干细胞中的LINE元件

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摘要

Heterochromatin is required to restrict aberrant expression of retrotransposons, but it remains poorly defined due to the underlying repeat-rich sequences. We dissected Suv39h-dependent histone H3 lysine 9 trimethylation (H3K9me3) by genome-wide ChIP sequencing in mouse embryonic stem cells (ESCs). Refined bioinformatic analyses of repeat subfamilies indicated selective accumulation of Suv39h-dependent H3K9me3 at interspersed repetitive elements that cover ~5% of the ESC epigenome. The majority of the ~8,150 intact long interspersed nuclear elements (LINEs) and endogenous retroviruses (ERVs), but only a minor fraction of the >1.8 million degenerate and truncated LINEs/ERVs, are enriched for Suv39h-dependent H3K9me3. Transcriptional repression of intact LINEs and ERVs is differentially regulated by Suv39h and other chromatin modifiers in ESCs but governed by DNA methylation in committed cells. These data provide a function for Suv39h-dependent H3K9me3 chromatin to specifically repress intact LINE elements in the ESC epigenome.
机译:需要异染色质来限制逆转录转座子的异常表达,但由于潜在的重复序列丰富,其定义仍然很差。我们通过小鼠胚胎干细胞(ESC)中的全基因组ChIP测序解剖了Suv39h依赖的组蛋白H3赖氨酸9三甲基化(H3K9me3)。重复亚科的精细生物信息学分析表明Suv39h依赖的H3K9me3在散布的重复元件中选择性积累,该元件覆盖ESC表观基因组的5%。 〜8,150个完整的长散布的核元素(LINE)和内源性逆转录病毒(ERV)中的大多数,但是在> 180万个简并和截短的LINEs / ERV中,只有一小部分富含Suv39h依赖性H3K9me3。完整的LINE和ERV的转录抑制受ESC中Suv39h和其他染色质修饰剂的调节,但受定型细胞中DNA甲基化的控制。这些数据为依赖Suv39h的H3K9me3染色质提供了特异性抑制ESC表观基因组中完整的LINE元素的功能。

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