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首页> 外文期刊>The Journal of biological chemistry >Binding of DEAD-box helicase Dhh1 to the 5′-untranslated region of ASH1 mRNA represses localized translation of ASH1 in yeast cells
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Binding of DEAD-box helicase Dhh1 to the 5′-untranslated region of ASH1 mRNA represses localized translation of ASH1 in yeast cells

机译:DEAD-box解旋酶Dhh1与ASH1 mRNA 5'-非翻译区的结合抑制了酵母细胞中ASH1的局部翻译

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Local translation of specific mRNAs is regulated by dynamic changes in their subcellular localization, and these changes are due to complex mechanisms controlling cytoplasmic mRNA transport. The budding yeast Saccharomyces cerevisiae is well suited to studying these mechanisms because many of its transcripts are transported from the mother cell to the budding daughter cell. Here, we investigated the translational control of ASH1 mRNA after transport and localization. We show that although ASH1 transcripts were translated after they reached the bud tip, some mRNAs were bound by the RNA-binding protein Puf6 and were non-polysomal. We also found that the DEAD-box helicase Dhh1 complexed with the untranslated ASH1 mRNA and Puf6. Loss of Dhh1 affected local translation of ASH1 mRNA and resulted in delocalization of ASH1 transcript in the bud. Forcibly shifting the non-polysomal ASH1 mRNA into polysomes was associated with Dhh1 dissociation. We further demonstrated that Dhh1 is not recruited to ASH1 mRNA co-transcriptionally, suggesting that it could bind to ASH1 mRNA within the cytoplasm. Of note, Dhh1 bound to the 5′-UTR of ASH1 mRNA and inhibited its translation in vitro. These results suggest that after localization to the bud tip, a portion of the localized ASH1 mRNA becomes translationally inactive because of binding of Dhh1 and Puf6 to the 5′- and 3′-UTRs of ASH1 mRNA.
机译:特定mRNA的局部翻译受其亚细胞定位动态变化的调节,而这些变化是由于控制细胞质mRNA转运的复杂机制所致。出芽的酵母啤酒酵母非常适合研究这些机制,因为其许多转录物都从母细胞转运到出芽的子细胞。在这里,我们调查了运输和本地化后ASH1 mRNA的翻译控制。我们显示,虽然ASH1转录本到达芽尖后已翻译,但某些mRNA仍受RNA结合蛋白Puf6结合,并且不是多聚体。我们还发现DEAD框解旋酶Dhh1与未翻译的ASH1 mRNA和Puf6复合。 Dhh1的丢失影响ASH1 mRNA的本地翻译,并导致芽中ASH1转录本的脱位。强制将非多体ASH1 mRNA转移到多核糖体中与Dhh1的解离有关。我们进一步证明,Dhh1不能通过转录共募集到ASH1 mRNA,这表明它可以与细胞质中的ASH1 mRNA结合。值得注意的是,Dhh1与ASH1 mRNA的5'-UTR结合并在体外抑制其翻译。这些结果表明,定位到芽尖后,由于Dhh1和Puf6与ASH1 mRNA的5'-和3'-UTR结合,因此定位的ASH1 mRNA的一部分变得翻译失活。

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