Department of Neurology, Ulm University, Albert-Einstein-Allee 11, 89081, Ulm, Germany.
German Center For Neurodegenerative Diseases (DZNE) Ulm, Ulm, Germany.
Mol Neurobiol. 2023 Jul;60(7):3898-3910. doi: 10.1007/s12035-023-03330-x. Epub 2023 Mar 29.
The fragile X protein (FXP) family comprises the multifunctional RNA-binding proteins FMR1, FXR1, and FXR2 that play an important role in RNA metabolism and regulation of translation, but also in DNA damage and cellular stress responses, mitochondrial organization, and more. FMR1 is well known for its implication in neurodevelopmental diseases. Recent evidence suggests substantial contribution of this protein family to amyotrophic lateral sclerosis (ALS) pathogenesis. ALS is a highly heterogeneous neurodegenerative disease with multiple genetic and unclear environmental causes and very limited treatment options. The loss of motoneurons in ALS is still poorly understood, especially because pathogenic mechanisms are often restricted to patients with mutations in specific causative genes. Identification of converging disease mechanisms evident in most patients and suitable for therapeutic intervention is therefore of high importance. Recently, deregulation of the FXPs has been linked to pathogenic processes in different types of ALS. Strikingly, in many cases, available data points towards loss of expression and/or function of the FXPs early in the disease, or even at the presymptomatic state. In this review, we briefly introduce the FXPs and summarize available data about these proteins in ALS. This includes their relation to TDP-43, FUS, and ALS-related miRNAs, as well as their possible contribution to pathogenic protein aggregation and defective RNA editing. Furthermore, open questions that need to be addressed before definitively judging suitability of these proteins as novel therapeutic targets are discussed.
脆性 X 蛋白 (FXP) 家族包括多功能 RNA 结合蛋白 FMR1、FXR1 和 FXR2,它们在 RNA 代谢和翻译调控中发挥重要作用,但也在 DNA 损伤和细胞应激反应、线粒体组织等方面发挥作用。FMR1 因其与神经发育疾病的关系而广为人知。最近的证据表明,该蛋白家族对肌萎缩侧索硬化症 (ALS) 的发病机制有很大的贡献。ALS 是一种高度异质性的神经退行性疾病,具有多种遗传和不明环境原因,且治疗选择非常有限。ALS 中运动神经元的丧失仍知之甚少,特别是因为致病机制通常仅限于特定致病基因发生突变的患者。因此,确定在大多数患者中明显存在的趋同疾病机制并适合治疗干预非常重要。最近,FXPs 的失调与不同类型 ALS 的致病过程有关。引人注目的是,在许多情况下,现有数据表明 FXPs 的表达和/或功能在疾病早期甚至在症状前状态就已经丧失。在这篇综述中,我们简要介绍了 FXPs,并总结了这些蛋白在 ALS 中的现有数据。这包括它们与 TDP-43、FUS 和 ALS 相关 miRNA 的关系,以及它们对致病蛋白聚集和缺陷 RNA 编辑的可能贡献。此外,还讨论了在明确判断这些蛋白作为新型治疗靶点的适用性之前需要解决的悬而未决的问题。