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The Paf1 Complex Represses ARG1 Transcription in Saccharomyces cerevisiae by Promoting Histone Modifications

机译:Paf1复合体通过促进组蛋白修饰抑制酿酒酵母中的ARG1转录。

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The conserved multifunctional Paf1 complex is important for the proper transcription of numerous genes, and yet the exact mechanisms by which it controls gene expression remain unclear. While previous studies indicate that the Paf1 complex is a positive regulator of transcription, the repression of many genes also requires the Paf1 complex. In this study we used ARG1 as a model gene to study transcriptional repression by the Paf1 complex in Saccharomyces cerevisiae. We found that several members of the Paf1 complex contribute to ARG1 repression and that the complex localizes to the ARG1 promoter and coding region in repressing conditions, which is consistent with a direct repressive function. Furthermore, Paf1 complex-dependent histone modifications are enriched at the ARG1 locus in repressing conditions, and histone H3 lysine 4 methylation contributes to ARG1 repression. Consistent with previous reports, histone H2B monoubiquitylation, the mark upstream of histone H3 lysine 4 methylation, is also important for ARG1 repression. To begin to identify the mechanistic basis for Paf1 complex-mediated repression of ARG1, we focused on the Rtf1 subunit of the complex. Through an analysis of RTF1 mutations that abrogate known Rtf1 activities, we found that Rtf1 mediates ARG1 repression primarily by facilitating histone modifications. Other members of the Paf1 complex, such as Paf1, appear to repress ARG1 through additional mechanisms. Together, our results suggest that Rtf1-dependent histone H2B ubiquitylation and H3 K4 methylation repress ARG1 expression and that histone modifications normally associated with active transcription can occur at repressed loci and contribute to transcriptional repression.
机译:保守的多功能Paf1复合物对于众多基因的正确转录很重要,但是尚不清楚其控制基因表达的确切机制。尽管先前的研究表明Paf1复合物是转录的正调节剂,但许多基因的抑制也需要Paf1复合物。在这项研究中,我们使用 ARG1 作为模型基因来研究酿酒酵母中Paf1复合体的转录抑制。我们发现Paf1复合物的几个成员有助于 ARG1 的阻遏,并且该复合物在阻遏条件下定位于 ARG1 启动子和编码区,这与直接阻遏相一致功能。此外,在抑制条件下,Paf1依赖复合物的组蛋白修饰在 ARG1 位点富集,而组蛋白H3赖氨酸4甲基化有助于 ARG1 抑制。与以前的报道一致,组蛋白H3赖氨酸4甲基化上游的标记组蛋白H2B单泛素化对 ARG1 抑制也很重要。为了确定Paf1复合物介导的 ARG1 阻遏的机制基础,我们集中于复合物的Rtf1亚基。通过对废除已知Rtf1活性的 RTF1 突变的分析,我们发现Rtf1主要通过促进组蛋白修饰来介导 ARG1 抑制。 Paf1复合体的其他成员,例如Paf1,似乎通过其他机制抑制了 ARG1 。在一起,我们的结果表明,依赖Rtf1的组蛋白H2B泛素化和H3 K4甲基化抑制 ARG1 表达,并且通常与活性转录相关的组蛋白修饰可发生在受抑制的基因座上,并有助于转录抑制。

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