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The Grand Challenge of Characterizing Ribonucleoprotein Networks

机译:表征核糖蛋白网络的巨大挑战

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Protein–RNA interactions are at the heart of cell regulation. From transcription, processing, storage, and translation, all the stages in the life cycle of an RNA depend on interactions with proteins. Although technologies are making remarkable progress in unraveling the landscape of protein–RNAinteractions,manykeyissuesareunclear.Westillhavetoidentifyhowmanyproteins haveRNA-bindingability,whataretheirtargetsandfunctionalpathways.Moreover,whileweknow the number of protein-coding genes in the human genome, functional non-coding RNAs are still poorly de?ned. What is the function of the non-coding part of the eukaryotic transcriptome? A clearunderstandingofthebiologicalfunctionsofcodingandnon-codingtranscriptswouldprovide novel insights in molecular biology. What are the protein components binding to an RNA while it is being produced? Our lack of understanding of how ribonucleoprotein complexes assemble is a major rate-limiting factor to future progress in the ?eld. We need to generate an in-depth characterization of protein–RNA complexes that form in cells during development and in response to external stimuli.
机译:蛋白质-RNA相互作用是细胞调节的核心。从转录,加工,存储和翻译来看,RNA生命周期的所有阶段都取决于与蛋白质的相互作用。尽管技术在揭示蛋白质与RNA相互作用的领域方面取得了显着进展,但许多关键问题尚不清楚。Westill能够确定许多蛋白质具有RNA结合能力的方式,它们的靶标和功能途径。此外,尽管我们知道人类基因组中蛋白质编码基因的数量,但功能性非编码RNA的定义仍然很差。真核转录组的非编码部分的功能是什么?对编码和非编码转录本的生物学功能的清楚理解将为分子生物学提供新的见解。产生RNA时,与RNA结合的蛋白质成分是什么?我们对核糖核蛋白复合物的组装方式缺乏了解是影响该领域未来进展的主要限速因素。我们需要对发育过程中以及对外部刺激做出反应的细胞中形成的蛋白质-RNA复合物进行深入表征。

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