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The enhancer of decapping proteins, Edc1p and Edc2p, bind RNA and stimulate the activity of the decapping enzyme

机译:解封蛋白的增强子Edc1p和Edc2p与RNA结合并刺激解封酶的活性

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摘要

A major pathway of eukaryotic mRNA turnover initiates with deadenylation, which allows a decapping reaction leading to 5′–3′ exonucleolytic degradation. A key control point in this pathway is the decapping of the mRNA. Two proteins, Edc1 and Edc2, were genetically identified previously as enhancers of the decapping reaction. In this work, we demonstrate that Edc1p and Edc2p are RNA-binding proteins. In addition, recombinant Edc1p or Edc2p stimulates mRNA decapping in cell-free extracts or with purified decapping enzyme. These results suggest that Edc1p and Edc2p activate decapping directly by binding to the mRNA substrate and enhancing the activity of the decapping enzyme. Interestingly, edc1Δ strains show defects in utilization of glycerol as a carbon source and misregulation of several mRNAs in response to carbon-source changes. This identifies a critical role for decapping and Edc1p in alterations of gene expression in response to carbon-source changes.
机译:真核生物mRNA更新的主要途径始于腺苷酸化,这可以导致脱盖反应,导致5'-3'外切核酸降解。该途径中的关键控制点是mRNA的脱盖。先前从基因上鉴定了两种蛋白质,Edc1和Edc2,可以作为脱盖反应的增强子。在这项工作中,我们证明Edc1p和Edc2p是RNA结合蛋白。此外,重组的Edc1p或Edc2p可以刺激无细胞提取物中或纯化的脱盖酶对mRNA的脱盖。这些结果表明,Edc1p和Edc2p通过与mRNA底物结合并增强去盖酶的活性来直接激活去盖作用。有趣的是,edc1Δ菌株在利用甘油作为碳源以及响应碳源变化而调节若干mRNA时显示出缺陷。这确定了响应碳源变化而在基因表达改变中脱盖和Edc1p的关键作用。

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