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肌萎缩侧索硬化症基因的可变剪接:失调与潜在治疗策略。

Alternative Splicing of ALS Genes: Misregulation and Potential Therapies.

机构信息

Institute for Biomedical Research and Innovation, National Research Council, Mangone, Cosenza, Italy.

Institute for Biomedical Research and Innovation, National Research Council, Catania, Italy.

出版信息

Cell Mol Neurobiol. 2020 Jan;40(1):1-14. doi: 10.1007/s10571-019-00717-0. Epub 2019 Aug 5.

DOI:10.1007/s10571-019-00717-0
PMID:31385134
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11448865/
Abstract

Neurodegenerative disorders such as amyotrophic lateral sclerosis (ALS), spinal muscular atrophy (SMA), Parkinson's, Alzheimer's, and Huntington's disease affect a rapidly increasing population worldwide. Although common pathogenic mechanisms have been identified (e.g., protein aggregation or dysfunction, immune response alteration and axonal degeneration), the molecular events underlying timing, dosage, expression, and location of RNA molecules are still not fully elucidated. In particular, the alternative splicing (AS) mechanism is a crucial player in RNA processing and represents a fundamental determinant for brain development, as well as for the physiological functions of neuronal circuits. Although in recent years our knowledge of AS events has increased substantially, deciphering the molecular interconnections between splicing and ALS remains a complex task and still requires considerable efforts. In the present review, we will summarize the current scientific evidence outlining the involvement of AS in the pathogenic processes of ALS. We will also focus on recent insights concerning the tuning of splicing mechanisms by epigenomic and epi-transcriptomic regulation, providing an overview of the available genomic technologies to investigate AS drivers on a genome-wide scale, even at a single-cell level resolution. In the future, gene therapy strategies and RNA-based technologies may be utilized to intercept or modulate the splicing mechanism and produce beneficial effects against ALS.

摘要

神经退行性疾病,如肌萎缩侧索硬化症(ALS)、脊髓性肌萎缩症(SMA)、帕金森病、阿尔茨海默病和亨廷顿病,正在影响全球范围内不断增加的人口。尽管已经确定了常见的发病机制(例如,蛋白质聚集或功能障碍、免疫反应改变和轴突退化),但 RNA 分子的时间、剂量、表达和位置的分子事件的基础仍未完全阐明。特别是可变剪接(AS)机制是 RNA 处理的关键因素,是大脑发育以及神经元回路生理功能的基本决定因素。尽管近年来我们对 AS 事件的认识有了很大的提高,但破译剪接与 ALS 之间的分子联系仍然是一项复杂的任务,仍然需要相当大的努力。在本综述中,我们将总结目前的科学证据,概述 AS 在 ALS 发病过程中的作用。我们还将重点介绍最近关于表观遗传和 epi-transcriptomic 调控对剪接机制的调节的见解,提供可用于在全基因组范围内,甚至在单细胞分辨率水平上研究 AS 驱动因素的基因组技术概述。在未来,基因治疗策略和基于 RNA 的技术可能被用于截获或调节剪接机制,并对 ALS 产生有益的影响。

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本文引用的文献

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RNA Dysregulation in Amyotrophic Lateral Sclerosis.肌萎缩侧索硬化症中的RNA失调
Front Genet. 2019 Jan 22;9:712. doi: 10.3389/fgene.2018.00712. eCollection 2018.
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RNA-Seq profiling in peripheral blood mononuclear cells of amyotrophic lateral sclerosis patients and controls.肌萎缩侧索硬化症患者和对照者外周血单个核细胞的 RNA-Seq 分析。
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Epigenetic regulation of alternative splicing.可变剪接的表观遗传调控
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ALS-implicated protein TDP-43 sustains levels of STMN2, a mediator of motor neuron growth and repair.TDP-43 是肌萎缩性侧索硬化症(ALS)相关蛋白,可维持运动神经元生长和修复的介质 STMN2 的水平。
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