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An Early Function during Transcription for the Yeast mRNA Export Factor Dbp5p/Rat8p Suggested by Its Genetic and Physical Interactions with Transcription Factor IIH Components

机译:酵母mRNA出口因子Dbp5p / Rat8p在转录过程中的早期功能由其与转录因子IIH成分的遗传和物理相互作用暗示

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摘要

The yeast DEAD-box protein Dbp5p/Rat8p is an essential factor for mRNA export and shuttles between the nucleus and the cytoplasm. It is concentrated at the cytoplasmic fibrils of the nuclear pore complex where it interacts with several nucleoporins. On the basis of this localization, it has been suggested that it might participate in a terminal step of RNA export, the release from the mRNA of proteins that accompany the mRNA during translocation through nuclear pores. In this report, we present evidence linking Dbp5p to transcription. Two different screens identified genetic interactions between DBP5 and genes involved in early transcription events, initiation and promoter clearance. Mutations of transcription proteins expected to impair transcription act as suppressors of dbp5 mutants, whereas those that may act to increase transcription are synthetically lethal with dbp5 mutations. We also show that growth and mRNA export in dbp5 mutant strains are dependent on the carboxy-terminal domain of the RNA pol II largest subunit. Finally, we show that Dbp5p associates physically with components of transcription factor IIH. Because these interactions affect not only growth but also mRNA export, they are likely to reflect a functional relationship between Dbp5p and the transcription machinery. Together, our results suggest a nuclear role for Dbp5 during the early steps of transcription.
机译:酵母DEAD-box蛋白Dbp5p / Rat8p是mRNA输出以及细胞核与细胞质之间穿梭的重要因素。它集中在核孔复合体的细胞质原纤维上,在这里它与几种核孔蛋白相互作用。基于这种定位,已经暗示它可能参与RNA输出的最终步骤,即在通过核孔易位期间伴随mRNA的蛋白质从mRNA释放。在本报告中,我们提供了将Dbp5p与转录联系起来的证据。两种不同的筛选鉴定了DBP5与参与早期转录事件,起始和启动子清除的基因之间的遗传相互作用。预期会破坏转录的转录蛋白突变可充当dbp5突变体的抑制剂,而那些可能起到增加转录作用的转录蛋白在合成上具有dbp5突变致死性。我们还显示dbp5突变株中的生长和mRNA出口取决于RNA pol II最大亚基的羧基末端结构域。最后,我们显示Dbp5p在物理上与转录因子IIH的成分相关联。因为这些相互作用不仅影响生长,而且影响mRNA的输出,所以它们很可能反映了Dbp5p与转录机制之间的功能关系。在一起,我们的结果表明Dbp5在转录的早期阶段的核作用。

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