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α-突触核蛋白的多个区域与帕金森病相关。

Multiple regions of alpha-synuclein are associated with Parkinson's disease.

作者信息

Mueller Jakob C, Fuchs Julia, Hofer Anne, Zimprich Alexander, Lichtner Peter, Illig Thomas, Berg Daniela, Wüllner Ullrich, Meitinger Thomas, Gasser Thomas

机构信息

Institute for Human Genetics, GSF-National Research Centre for Environment and Health, Neuherberg, Germany.

出版信息

Ann Neurol. 2005 Apr;57(4):535-41. doi: 10.1002/ana.20438.

Abstract

alpha-Synuclein is considered to play an important role in the pathogenesis of both the rare familial and the common sporadic forms of Parkinson's disease. Previous reports primarily have tested the association of alpha-synuclein promoter polymorphisms with idiopathic Parkinson's disease, but results are controversial. We first characterized the linkage disequilibrium structure of the alpha-synuclein gene region with a dense set of 56 genetic markers and subsequently performed two independent case-control association analyses using tagging markers. We could distinguish two large linkage disequilibrium blocks spanning the alpha-synuclein gene. Several markers within the 3'-block around exons 5 and 6 showed strong association with Parkinson's disease (p = 0.00009). Effects of the associated variants might be mediated by regulatory elements in this highly conserved region or by a frequency shift in a previously described splice variant lacking exon 5. A direct association with promoter polymorphisms could not be replicated in our sample set. A second set of markers in the 5'-block of the gene were also significantly associated with Parkinson's disease, when young patients and female subjects were analyzed separately. These findings indicate locus heterogeneity for the pathogenesis of Parkinson's disease in different genetic or physiological environments, related to sex and age.

摘要

α-突触核蛋白被认为在罕见的家族性和常见的散发性帕金森病的发病机制中起重要作用。先前的报告主要检测了α-突触核蛋白启动子多态性与特发性帕金森病的关联,但结果存在争议。我们首先用一组密集的56个遗传标记对α-突触核蛋白基因区域的连锁不平衡结构进行了表征,随后使用标签标记进行了两项独立的病例对照关联分析。我们可以区分跨越α-突触核蛋白基因的两个大的连锁不平衡块。外显子5和6周围3'-块内的几个标记与帕金森病显示出强烈关联(p = 0.00009)。相关变体的作用可能由这个高度保守区域中的调控元件介导,或者由先前描述的缺乏外显子5的剪接变体中的频率偏移介导。在我们的样本集中无法复制与启动子多态性的直接关联。当分别分析年轻患者和女性受试者时,该基因5'-块中的第二组标记也与帕金森病显著相关。这些发现表明,在与性别和年龄相关的不同遗传或生理环境中,帕金森病发病机制存在基因座异质性。

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