Andreassi Catia, Crerar Hamish, Riccio Antonella
MRC Laboratory for Molecular Cell Biology, University College London, London, United Kingdom.
Front Mol Neurosci. 2018 Aug 28;11:304. doi: 10.3389/fnmol.2018.00304. eCollection 2018.
Neurons are morphologically complex cells that rely on the compartmentalization of protein expression to develop and maintain their extraordinary cytoarchitecture. This formidable task is achieved, at least in part, by targeting mRNA to subcellular compartments where they are rapidly translated. mRNA transcripts are the conveyor of genetic information from DNA to the translational machinery, however, they are also endowed with additional functions linked to both the coding sequence (open reading frame, or ORF) and the flanking 5' and 3' untranslated regions (UTRs), that may harbor coding-independent functions. In this review, we will highlight recent evidences supporting new coding-dependent and -independent functions of mRNA and discuss how nuclear and cytoplasmic post-transcriptional modifications of mRNA contribute to localization and translation in mammalian cells with specific emphasis on neurons. We also describe recently developed techniques that can be employed to study RNA dynamics at subcellular level in eukaryotic cells in developing and regenerating neurons.
神经元是形态复杂的细胞,它们依靠蛋白质表达的区室化来发育和维持其非凡的细胞结构。至少部分地,通过将mRNA靶向到能快速翻译的亚细胞区室来完成这项艰巨的任务。mRNA转录本是从DNA到翻译机器的遗传信息传递者,然而,它们还具有与编码序列(开放阅读框,或ORF)以及侧翼的5'和3'非翻译区(UTR)相关的额外功能,这些区域可能具有不依赖编码的功能。在这篇综述中,我们将重点介绍支持mRNA新的编码依赖性和非依赖性功能的最新证据,并讨论mRNA的核内和胞质转录后修饰如何促进哺乳动物细胞中的定位和翻译,特别强调神经元。我们还描述了最近开发的技术,这些技术可用于研究发育中和再生神经元的真核细胞中亚细胞水平的RNA动态。