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Post-transcriptional Processing of mRNA in Neurons: The Vestiges of the RNA World Drive Transcriptome Diversity

机译:神经元中mRNA的转录后处理:RNA世界的遗迹驱动转录组多样性。

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摘要

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.
机译:神经元是形态复杂的细胞,依赖于蛋白质表达的区室化来发展和维持其非凡的细胞结构。这项艰巨的任务至少部分是通过将mRNA靶向亚细胞区室来实现的,亚细胞区室将它们快速翻译。 mRNA转录物是遗传信息从DNA传递到翻译机器的载体,但是它们也具有与编码序列(开放阅读框或ORF)以及侧翼5'和3'非翻译区(UTR)相关的附加功能),可能包含与编码无关的功能。在这篇综述中,我们将重点介绍支持mRNA的新编码依赖性和非依赖性功能的最新证据,并讨论mRNA的核和细胞质转录后修饰如何促进哺乳动物细胞中的定位和翻译,尤其着重于神经元。我们还描述了最近开发的技术,可用于研究发育和再生神经元的真核细胞中亚细胞水平的RNA动力学。

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