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Gcn5-mediated acetylation at MBF-regulated promoters induces the G1/S transcriptional wave

机译:MBcn调控启动子上的Gcn5介导的乙酰化诱导G1 / S转录波

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摘要

In fission yeast, MBF-dependent transcription is inactivated at the end of S phase through a negative feedback loop that involves the co-repressors, Yox1 and Nrm1. Although this repression system is well known, the molecular mechanisms involved in MBF activation remain largely unknown. Compacted chromatin constitutes a barrier to activators accessing promoters. Here, we show that chromatin regulation plays a key role in activating MBF-dependent transcription. Gcn5, a part of the SAGA complex, binds to MBF-regulated promoters through the MBF co-activator Rep2 in a cell cycle-dependent manner and in a reverse correlation to the binding of the MBF co-repressors, Nrm1 or Yox1. We propose that the co-repressors function as physical barriers to SAGA recruitment onto MBF promoters. We also show that Gcn5 acetylates specific lysine residues on histone H3 in a cell cycle-regulated manner. Furthermore, either in a mutant or in a strain in which histone H3 is kept in an unacetylated form, MBF-dependent transcription is downregulated. In summary, Gcn5 is required for the full activation and correct timing of MBF-regulated gene transcription.
机译:在裂变酵母中,MBF依赖性转录在S期末通过负反馈回路失活,该负反馈回路涉及共抑制子Yox1和Nrm1。尽管该阻抑系统是众所周知的,但与MBF激活有关的分子机制仍然未知。紧密染色质构成了激活剂进入启动子的障碍。在这里,我们表明染色质调节在激活MBF依赖性转录中起关键作用。 SACN复合体的一部分Gcn5通过MBF共激活因子Rep2以细胞周期依赖性方式与MBF调控的启动子结合,并与MBF共抑制因子Nrm1或Yox1的反向相关。我们建议,共阻遏物充当SAGA募集到MBF启动子的物理障碍。我们还显示,Gcn5以细胞周期调节的方式乙酰化组蛋白H3上的特定赖氨酸残基。此外,在突变体或组蛋白H3保持未乙酰化形式的菌株中,MBF依赖性转录被下调。总之,Gcn5是MBF调控的基因转录的完全激活和正确时机所必需的。

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