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首页> 外文期刊>Journal of Neural Transmission >The dynactin p150 subunit: cell biology studies of sequence changes found in ALS/MND and Parkinsonian Syndromes
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The dynactin p150 subunit: cell biology studies of sequence changes found in ALS/MND and Parkinsonian Syndromes

机译:Dynactin p150亚基:在ALS / MND和帕金森综合症中发现的序列变化的细胞生物学研究

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摘要

The dynactin p150glued subunit, encoded by the gene DCTN1 is part of the dynein–dynactin motor protein complex responsible for retrograde axonal transport. This subunit is a candidate modifier for neurodegenerative diseases, in particular motoneuron and extrapyramidal diseases. Based on an extensive screening effort of all 32 exons in more than 2,500 ALS/MND patients, patients suffering from Parkinsonian Syndromes and controls, we investigated 24 sequence variants of p150 in cell-based studies. We used both non-neuronal cell lines and primary rodent spinal motoneurons and report on cell biological abnormalities in five of these sequence alterations and also briefly report on the clinical features. Our results suggest the presence of biological changes caused by some p150 mutants pointing to a potential pathogenetic significance as modifier of the phenotype of the human disease.
机译:由DCTN1基因编码的dynactin p150胶合的亚基是负责逆行轴突运输的dynein-dynactin运动蛋白复合物的一部分。该亚基是神经退行性疾病,特别是运动神经元和锥体外系疾病的候选修饰物。基于对超过2500名ALS / MND患者,帕金森综合征和对照患者的全部32个外显子的广泛筛选,我们在基于细胞的研究中研究了p150的24个序列变体。我们同时使用了非神经元细胞系和啮齿动物原发性脊髓运动神经元,并在其中五个序列改变中报告了细胞生物学异常,并简要报告了临床特征。我们的研究结果表明存在由某些p150突变体引起的生物学变化,这些突变表明潜在的病原学意义是人类疾病表型的修饰因子。

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