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SAGA DUBm-mediated surveillance regulates prompt export of stress-inducible transcripts for proteostasis

机译:SAGA DUBm介导的监测可调节应激诱导的转录本对蛋白稳态的迅速输出

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摘要

During stress, prompt export of stress-inducible transcripts is critical for cell survival. Here, we characterize a function of the SAGA (Spt-Ada-Gcn5 acetyltransferase) deubiquitylating module (DUBm) in monitoring messenger ribonucleoprotein (mRNP) biogenesis to regulate non-canonical mRNA export of stress-inducible transcripts. Our genetic and biochemical analyses suggest that there is a functional relationship between Sgf73p of DUBm and the essential mRNA export factor, Yra1p. Under physiological conditions, Sgf73p is critical for the proper chromatin localization and RNA binding of Yra1p, while also quality controlling the biogenesis of mRNPs in conjunction with the nuclear exosome exonuclease, Rrp6p. Under environmental stress, when immediate transport of stress-inducible transcripts is imperative, Sgf73p facilitates the bypass of canonical surveillance and promotes the timely export of necessary transcripts. Overall, our results show that the Sgf73p-mediated plasticity of gene expression is important for the ability of cells to tolerate stress and regulate proteostasis to survive under environmental uncertainty.
机译:在压力下,迅速导出压力诱导型转录本对于细胞存活至关重要。在这里,我们表征了SAGA(Spt-Ada-Gcn5乙酰转移酶)去泛素化模块(DUBm)在监测信使核糖核蛋白(mRNP)生物发生以调节压力诱导转录本的非规范mRNA输出中的功能。我们的遗传和生化分析表明,DUBm的Sgf73p与必需的mRNA出口因子Yra1p之间存在功能关系。在生理条件下,Sgf73p对于适当的染色质定位和Yra1p的RNA结合至关重要,同时还需要质量控制mRNP与核外泌体核酸外切酶Rrp6p的生物合成。在环境压力下,当迫切需要胁迫诱导的转录本运输时,Sgf73p有助于绕开规范的监测并促进及时输出必要的转录本。总体而言,我们的结果表明,Sgf73p介导的基因表达可塑性对于细胞耐受压力和调节蛋白稳定在环境不确定性下生存的能力至关重要。

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