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在一个携带 TARDBP 中 p.Y374X 截断突变的 ALS 家系中存在非典型 TDP-43 蛋白表达。

Atypical TDP-43 protein expression in an ALS pedigree carrying a p.Y374X truncation mutation in TARDBP.

机构信息

Sheffield Institute for Translational Neuroscience (SITraN), University of Sheffield, Sheffield, UK.

Nuffield Department of Clinical Neurosciences, University of Oxford, Oxford, UK.

出版信息

Brain Pathol. 2023 Jan;33(1):e13104. doi: 10.1111/bpa.13104. Epub 2022 Jul 24.

Abstract

We describe an autosomal dominant, multi-generational, amyotrophic lateral sclerosis (ALS) pedigree in which disease co-segregates with a heterozygous p.Y374X nonsense mutation within TDP-43. Mislocalization of TDP-43 and formation of insoluble TDP-43-positive neuronal cytoplasmic inclusions is the hallmark pathology in >95% of ALS patients. Neuropathological examination of the single case for which CNS tissue was available indicated typical TDP-43 pathology within lower motor neurons, but classical TDP-43-positive inclusions were absent from motor cortex. The mutated allele is transcribed and translated in patient fibroblasts and motor cortex tissue, but overall TDP-43 protein expression is reduced compared to wild-type controls. Despite absence of TDP-43-positive inclusions we confirmed deficient TDP-43 splicing function within motor cortex tissue. Furthermore, urea fractionation and mass spectrometry of motor cortex tissue carrying the mutation revealed atypical TDP-43 protein species but not typical C-terminal fragments. We conclude that the p.Y374X mutation underpins a monogenic, fully penetrant form of ALS. Reduced expression of TDP-43 combined with atypical TDP-43 protein species and absent C-terminal fragments extends the molecular phenotypes associated with TDP-43 mutations and with ALS more broadly. Future work will need to include the findings from this pedigree in dissecting the mechanisms of TDP-43-mediated toxicity.

摘要

我们描述了一个常染色体显性、多代、肌萎缩侧索硬化症(ALS)家系,该家系中疾病与 TDP-43 内的杂合 p.Y374X 无义突变共分离。TDP-43 的定位错误和不溶性 TDP-43 阳性神经元细胞质内含物的形成是>95%的 ALS 患者的标志性病理学特征。对唯一可获得中枢神经系统组织的病例进行神经病理学检查表明,在较低的运动神经元中存在典型的 TDP-43 病理学,但在运动皮层中不存在经典的 TDP-43 阳性包涵体。突变等位基因在患者成纤维细胞和运动皮层组织中转录和翻译,但与野生型对照相比,总 TDP-43 蛋白表达减少。尽管不存在 TDP-43 阳性包涵体,我们仍在运动皮层组织中证实了 TDP-43 剪接功能的缺陷。此外,携带该突变的运动皮层组织的尿素分级和质谱分析显示出异常的 TDP-43 蛋白种类,但没有典型的 C 末端片段。我们得出结论,p.Y374X 突变是一种单基因、完全外显的 ALS 形式。TDP-43 表达减少,与异常 TDP-43 蛋白种类和缺乏 C 末端片段相结合,扩大了与 TDP-43 突变和更广泛的 ALS 相关的分子表型。未来的工作需要将该家系的发现纳入解析 TDP-43 介导的毒性机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac46/9836368/4bf3e610c8c6/BPA-33-e13104-g003.jpg

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