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脊髓小脑共济失调 3 型/马查多-约瑟夫病中 ATXN3 剪接变异体在血液和小脑中的丰度。

Blood and cerebellar abundance of ATXN3 splice variants in spinocerebellar ataxia type 3/Machado-Joseph disease.

机构信息

IBMC - Instituto de Biologia Molecular e Celular, i3S - Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Porto, Portugal; Faculdade de Ciências e Tecnologia, Universidade dos Açores, Ponta Delgada, Portugal.

Institute of Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany; Centre for Rare Diseases, University of Tübingen, Tübingen, Germany.

出版信息

Neurobiol Dis. 2024 Apr;193:106456. doi: 10.1016/j.nbd.2024.106456. Epub 2024 Feb 27.

Abstract

Spinocerebellar ataxia type 3 (SCA3)/Machado-Joseph disease (MJD) is a heritable proteinopathy disorder, whose causative gene, ATXN3, undergoes alternative splicing. Ataxin-3 protein isoforms differ in their toxicity, suggesting that certain ATXN3 splice variants may be crucial in driving the selective toxicity in SCA3. Using RNA-seq datasets we identified and determined the abundance of annotated ATXN3 transcripts in blood (n = 60) and cerebellum (n = 12) of SCA3 subjects and controls. The reference transcript (ATXN3-251), translating into an ataxin-3 isoform harbouring three ubiquitin-interacting motifs (UIMs), showed the highest abundance in blood, while the most abundant transcript in the cerebellum (ATXN3-208) was of unclear function. Noteworthy, two of the four transcripts that encode full-length ataxin-3 isoforms but differ in the C-terminus were strongly related with tissue expression specificity: ATXN3-251 (3UIM) was expressed in blood 50-fold more than in the cerebellum, whereas ATXN3-214 (2UIM) was expressed in the cerebellum 20-fold more than in the blood. These findings shed light on ATXN3 alternative splicing, aiding in the comprehension of SCA3 pathogenesis and providing guidance in the design of future ATXN3 mRNA-lowering therapies.

摘要

脊髓小脑共济失调 3 型(SCA3)/马查多-约瑟夫病(MJD)是一种遗传性蛋白病,其致病基因 ATXN3 经历可变剪接。 运动蛋白-3 蛋白异构体在其毒性方面存在差异,这表明某些 ATXN3 剪接变体可能在驱动 SCA3 的选择性毒性方面至关重要。 使用 RNA-seq 数据集,我们鉴定并确定了 SCA3 患者和对照组血液(n=60)和小脑(n=12)中注释的 ATXN3 转录本的丰度。 参考转录本(ATXN3-251),翻译为含有三个泛素相互作用基序(UIMs)的运动蛋白-3 异构体,在血液中丰度最高,而小脑中丰度最高的转录本(ATXN3-208)功能尚不清楚。 值得注意的是,编码全长运动蛋白-3 异构体但 C 末端不同的四个转录本中的两个与组织表达特异性密切相关:ATXN3-251(3UIM)在血液中的表达是小脑的 50 倍,而 ATXN3-214(2UIM)在小脑中的表达是血液的 20 倍。 这些发现阐明了 ATXN3 可变剪接,有助于理解 SCA3 的发病机制,并为未来 ATXN3 mRNA 降低疗法的设计提供指导。

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