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Identification of RNA recognition elements in the Saccharomyces cerevisiae transcriptome

机译:酿酒酵母转录组中RNA识别元件的鉴定。

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摘要

Post-transcriptional regulation of gene expression, including mRNA localization, translation and decay, is ubiquitous yet still largely unexplored. How is the post-transcriptional regulatory program of each mRNA encoded in its sequence? Hundreds of specific RNA-binding proteins (RBPs) appear to play roles in mediating the post-transcriptional regulatory program, akin to the roles of specific DNA-binding proteins in transcription. As a step toward decoding the regulatory programs encoded in each mRNA, we focused on specific mRNA-protein interactions. We computationally analyzed the sequences of Saccharomyces cerevisiae mRNAs bound in vivo by 29 specific RBPs, identifying eight novel candidate motifs and confirming or extending six earlier reported recognition elements. Biochemical selections for RNA sequences selectively recognized by 12 yeast RBPs yielded novel motifs bound by Pin4, Nsr1, Hrb1, Gbp2, Sgn1 and Mrn1, and recovered the known recognition elements for Puf3, She2, Vts1 and Whi3. Most of the RNA elements we uncovered were associated with coherent mRNA expression changes and were significantly conserved in related yeasts, supporting their functional importance and suggesting that the corresponding RNA-protein interactions are evolutionarily conserved.
机译:基因表达的转录后调控,包括mRNA定位,翻译和衰减,是普遍存在的,但仍未得到充分探索。每个mRNA的转录后调控程序如何在其序列中编码?数百种特定的RNA结合蛋白(RBP)似乎在介导转录后调控程序中发挥作用,类似于特定的DNA结合蛋白在转录中的作用。作为解码每个mRNA中编码的调控程序的一步,我们专注于特定的mRNA-蛋白质相互作用。我们通过计算分析了由29种特异性RBP体内结合的酿酒酵母mRNA的序列,确定了8个新的候选基序,并确认或扩展了6个较早报道的识别元件。通过12种酵母RBP选择性识别的RNA序列的生化选择产生了与Pin4,Nsr1,Hrb1,Gbp2,Sgn1和Mrn1结合的新基序,并回收了Puf3,She2,Vts1和Whi3的已知识别元件。我们发现的大多数RNA元件都与连贯的mRNA表达变化有关,并且在相关酵母中显着保守,从而支持了它们的功能重要性,并暗示了相应的RNA-蛋白质相互作用在进化上是保守的。

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