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Regulation of gene expression in mammalian nervous system through alternative pre-mRNA splicing coupled with RNA quality control mechanisms

机译:通过替代性的前mRNA剪接和RNA质量控制机制调节哺乳动物神经系统中的基因表达

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摘要

Eukaryotic gene expression is orchestrated on a genome-wide scale through several post-transcriptional mechanisms. Of these, alternative pre-mRNA splicing expands the proteome diversity and modulates mRNA stability through downstream RNA quality control (QC) pathways including nonsense-mediated decay (NMD) of mRNAs containing premature termination codons and nuclear retention and elimination (NRE) of intron-containing transcripts. Although originally identified as mechanisms for eliminating aberrant transcripts, a growing body of evidence suggests that NMD and NRE coupled with deliberate changes in pre-mRNA splicing patterns are also used in a number of biological contexts for deterministic control of gene expression. Here we review recent studies elucidating molecular mechanisms and biological significance of these gene regulation strategies with a specific focus on their roles in nervous system development and physiology. This article is part of a Special Issue entitled 'RNA and splicing regulation in neurodegeneration'.
机译:通过几种转录后机制,可以在全基因组范围内协调真核基因的表达。其中,替代性的pre-mRNA剪接可通过下游RNA质量控制(QC)途径扩展蛋白质组多样性并调节mRNA稳定性,这些途径包括无义介导的包含过早终止密码子的mRNA的衰变(NMD)和内含子的核保留和消除(NRE)。包含成绩单。尽管最初被确定为消除异常转录本的机制,但越来越多的证据表明,NMD和NRE加上前mRNA剪接模式的有意改变,也已在许多生物学背景下用于确定性控制基因表达。在这里,我们回顾了最近的研究,阐明了这些基因调控策略的分子机制和生物学意义,特别关注了它们在神经系统发育和生理中的作用。本文是名为“神经变性中的RNA和剪接调控”的特刊的一部分。

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