研究大脑中的 m6A:透视当前方法、挑战和未来方向

IF 3.5 3区 医学 Q2 NEUROSCIENCES
Matthew Tegowski, Kate D. Meyer
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引用次数: 0

摘要

细胞中转录后 RNA 调控的一个主要机制是对 RNA 核苷进行化学修饰,这几乎涉及 RNA 生命周期的方方面面。N6-甲基腺苷(m6A)是细胞 mRNA 和非编码 RNA 中一种非常普遍的修饰,在控制基因表达和细胞功能方面发挥着重要作用。在大脑中,适当调节 m6A 对神经发育、学习和记忆以及对损伤的反应至关重要,而 m6A 失调与多种神经系统疾病有关。因此,了解 m6A 及其在大脑中的调控方式对于揭示其在大脑功能中的作用以及确定治疗人类疾病的新途径非常重要。我们对 m6A 的了解主要得益于绘制和量化 m6A 位点的技术进步。在此,我们回顾了当前表征 m6A 的技术,并重点介绍了新出现的方法。我们讨论了当前工具的优势和局限性以及未来面临的主要挑战,并就这一领域的持续发展如何推动我们了解大脑中的 m6A 及其在脑部疾病中的作用提出了自己的观点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Studying m6A in the brain: a perspective on current methods, challenges, and future directions
A major mechanism of post-transcriptional RNA regulation in cells is the addition of chemical modifications to RNA nucleosides, which contributes to nearly every aspect of the RNA life cycle. N6-methyladenosine (m6A) is a highly prevalent modification in cellular mRNAs and non-coding RNAs, and it plays important roles in the control of gene expression and cellular function. Within the brain, proper regulation of m6A is critical for neurodevelopment, learning and memory, and the response to injury, and m6A dysregulation has been implicated in a variety of neurological disorders. Thus, understanding m6A and how it is regulated in the brain is important for uncovering its roles in brain function and potentially identifying novel therapeutic pathways for human disease. Much of our knowledge of m6A has been driven by technical advances in the ability to map and quantify m6A sites. Here, we review current technologies for characterizing m6A and highlight emerging methods. We discuss the advantages and limitations of current tools as well as major challenges going forward, and we provide our perspective on how continued developments in this area can propel our understanding of m6A in the brain and its role in brain disease.
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来源期刊
CiteScore
5.70
自引率
2.10%
发文量
669
审稿时长
14 weeks
期刊介绍: Frontiers in Molecular Neuroscience is a first-tier electronic journal devoted to identifying key molecules, as well as their functions and interactions, that underlie the structure, design and function of the brain across all levels. The scope of our journal encompasses synaptic and cellular proteins, coding and non-coding RNA, and molecular mechanisms regulating cellular and dendritic RNA translation. In recent years, a plethora of new cellular and synaptic players have been identified from reduced systems, such as neuronal cultures, but the relevance of these molecules in terms of cellular and synaptic function and plasticity in the living brain and its circuits has not been validated. The effects of spine growth and density observed using gene products identified from in vitro work are frequently not reproduced in vivo. Our journal is particularly interested in studies on genetically engineered model organisms (C. elegans, Drosophila, mouse), in which alterations in key molecules underlying cellular and synaptic function and plasticity produce defined anatomical, physiological and behavioral changes. In the mouse, genetic alterations limited to particular neural circuits (olfactory bulb, motor cortex, cortical layers, hippocampal subfields, cerebellum), preferably regulated in time and on demand, are of special interest, as they sidestep potential compensatory developmental effects.
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