School of Biological Sciences, Nanyang Technological University, Singapore 637551, Singapore.
Mol Cell Neurosci. 2013 Sep;56:420-8. doi: 10.1016/j.mcn.2013.01.003. Epub 2013 Jan 26.
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'.
真核生物基因表达是通过几种转录后机制在全基因组范围内进行调控的。在这些机制中,选择性的前体 mRNA 剪接通过下游 RNA 质量控制 (QC) 途径扩大蛋白质组的多样性,并调节 mRNA 的稳定性,包括含有无意义终止密码子的 mRNA 的无意义介导的衰变 (NMD) 和含有内含子的转录本的核滞留和消除 (NRE)。虽然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 与前体 mRNA 剪接模式的有意改变一起,也被用于许多生物学背景下,以确定基因表达的控制。在这里,我们综述了最近阐明这些基因调控策略的分子机制和生物学意义的研究,特别关注它们在神经系统发育和生理学中的作用。本文是题为“神经退行性疾病中的 RNA 和剪接调控”的特刊的一部分。