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重新下调 ataxin-2 的表达水平可下调突变型 ataxin-3 的翻译,从而缓解 Machado-Joseph 病。

Re-establishing ataxin-2 downregulates translation of mutant ataxin-3 and alleviates Machado-Joseph disease.

机构信息

1 CNC - Center for Neuroscience and Cell Biology, University of Coimbra, Rua Larga, FMUC, 3004- 504 Coimbra, Portugal.

1 CNC - Center for Neuroscience and Cell Biology, University of Coimbra, Rua Larga, FMUC, 3004- 504 Coimbra, Portugal 2 Faculty of Pharmacy, University of Coimbra, 3000-548 Coimbra, Portugal.

出版信息

Brain. 2015 Dec;138(Pt 12):3537-54. doi: 10.1093/brain/awv298. Epub 2015 Oct 21.

Abstract

Machado-Joseph disease is a progressive neurodegenerative disorder associated with the polyQ-expanded ataxin-3 (encoded by ATXN3), for which no therapy is available. With the aim of clarifying the mechanism of neurodegeneration, we hypothesized that the abnormally long polyQ tract would interact aberrantly with ataxin-2 (encoded by ATXN2), another polyQ protein whose function has recently been linked to translational regulation. Using patient's samples and cellular and animal's models we found that in Machado-Joseph disease: (i) ataxin-2 levels are reduced; and (ii) its subcellular localization is changed towards the nucleus. Restoring ataxin-2 levels by lentiviral-mediated overexpression: (i) reduced mutant ataxin-3 levels; and (ii) rescued behaviour defects and neuropathology in a transgenic mouse model of Machado-Joseph disease. Conversely (i) mutating the ataxin-2 motif that enables binding to its natural interactor and translation activator poly(A)-binding protein; or (ii) overexpressing poly(A)-binding protein, had opposite effects, increasing mutant ataxin-3 translation and aggregation. This work suggests that in Machado-Joseph disease, mutant ataxin-3 drives an abnormal reduction of ataxin-2 levels, which overactivates poly(A)-binding protein, increases translation of mutant ataxin-3 and other proteins and aggravates Machado-Joseph disease. Re-establishment of ataxin-2 levels reduces mutant ataxin-3 and alleviates Machado-Joseph disease pathogenesis opening a new avenue for therapeutic intervention in this and potentially other polyQ disorders.

摘要

马查多-约瑟夫病是一种进行性神经退行性疾病,与多聚谷氨酰胺扩展的ataxin-3(由 ATXN3 编码)有关,目前尚无治疗方法。为了阐明神经退行性变的机制,我们假设异常长的多聚谷氨酰胺片段会与另一种多聚谷氨酰胺蛋白 ataxin-2(由 ATXN2 编码)异常相互作用,后者的功能最近与翻译调控有关。使用患者样本以及细胞和动物模型,我们发现马查多-约瑟夫病中:(i)ataxin-2 水平降低;(ii)其亚细胞定位向核内改变。通过慢病毒介导的过表达恢复 ataxin-2 水平:(i)降低突变型 ataxin-3 水平;(ii)挽救了马查多-约瑟夫病转基因小鼠模型中的行为缺陷和神经病理学。相反,(i)突变使 ataxin-2 与天然相互作用蛋白和翻译激活蛋白 poly(A)-结合蛋白结合的基序;或(ii)过表达 poly(A)-结合蛋白,产生相反的效果,增加突变型 ataxin-3 的翻译和聚集。这项工作表明,在马查多-约瑟夫病中,突变型 ataxin-3 驱动异常降低 ataxin-2 水平,从而过度激活 poly(A)-结合蛋白,增加突变型 ataxin-3 和其他蛋白的翻译,并加重马查多-约瑟夫病。恢复 ataxin-2 水平可降低突变型 ataxin-3 并缓解马查多-约瑟夫病发病机制,为该疾病和其他潜在多聚谷氨酰胺疾病的治疗干预开辟了新途径。

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