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Distribution and Maintenance of Histone H3 Lysine 36 Trimethylation in Transcribed Locus

机译:转录基因座中组蛋白H3赖氨酸36三甲基化的分布和维持

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摘要

Post-translational modifications of core histones play an important role in the epigenetic regulation of chromatin dynamics and gene expression. In Saccharomyces cerevisiae methylation marks at K4, K36, and K79 of histone H3 are associated with gene transcription. Although Set2-mediated H3K36 methylation is enriched throughout the coding region of active genes and prevents aberrant transcriptional initiation within coding sequences, it is not known if transcription of one locus impacts the methylation pattern of neighbouring areas and for how long H3K36 methylation is maintained after transcription termination. Our results demonstrate that H3K36 methylation is restricted to the transcribed sequence only and the modification does not spread to adjacent loci downstream from transcription termination site. We also show that H3K36 trimethylation mark persists in the locus for at least 60 minutes after transcription inhibition, suggesting a short epigenetic memory for recently occurred transcriptional activity. Our results indicate that both replication-dependent exchange of nucleosomes and the activity of histone demethylases Rph1, Jhd1 and Gis1 contribute to the turnover of H3K36 methylation upon shut-down of transcription.
机译:核心组蛋白的翻译后修饰在染色质动力学和基因表达的表观遗传调控中起重要作用。在酿酒酵母中,组蛋白H3的K4,K36和K79处的甲基化标记与基因转录有关。尽管Set2介导的H3K36甲基化在整个活性基因的编码区域富集,并阻止了编码序列内异常的转录起始,但尚不清楚一个基因座的转录是否会影响邻近区域的甲基化模式,以及转录后H3K36甲基化能维持多长时间终止。我们的结果表明,H3K36甲基化仅限于转录的序列,并且修饰不会扩散到转录终止位点下游的相邻基因座。我们还显示,H3K36三甲基化标记在转录抑制后至少60分钟内在基因座中持续存在,表明最近发生的转录活性具有短暂的表观遗传记忆。我们的结果表明,核糖体的复制依赖性交换和组蛋白脱甲基酶Rph1,Jhd1和Gis1的活性都有助于转录关闭后H3K36甲基化的转换。

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