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人类无序蛋白1基因在晚发性阿尔茨海默病中的基因组组织鉴定、序列变异及作用分析

Identification of genomic organisation, sequence variants and analysis of the role of the human dishevelled 1 gene in late onset Alzheimer's disease.

作者信息

Russ C, Lovestone S, Powell J F

机构信息

Department of Neuroscience, Institute of Psychiatry, London SE5 8AF, UK.

出版信息

Mol Psychiatry. 2002;7(1):104-9. doi: 10.1038/sj.mp.4000941.

Abstract

Alzheimer's disease (AD) is a disorder characterised by a progressive deterioration in memory and other cognitive functions. Neurofibrillary tangles (NFT) are a major pathological hallmark of AD, these are aggregations of paired helical filaments (PHF) comprised of the hyperphosphorylated microtubule associated protein tau. Several kinases, such as glycogen synthase kinase 3 beta (GSK3beta) and c-Jun N-terminal kinase (JNK), phosphorylate tau at sites that are phosphorylated in PHF. Dishevelled 1 (DVL1) is thought to act as a positive regulator of the wnt signalling pathway, and inhibits GSK3beta activity preventing beta-catenin degradation and thus allowing wnt target gene expression. JNK activation is also regulated by DVL1, however it is unclear if this is via the wnt signalling pathway. These observations suggest a central role for DVL1 in tau phosphorylation and AD and led us to investigate DVL1 as a candidate gene for this disorder. We determined the genomic structure of the DVL1 gene by sequencing and data mining and searched for sequence variations in the coding sequences and flanking introns. The DVL1 gene spans a region of approximately 13.8 kb (not including the 5' untranslated region) and is encoded by 15 exons. Analysis of over 4.3 kb of sequence, including 98% of exonic sequences and introns 2, 3, 6, 7, 9, 10, 11 and 12, revealed there to be six rare (< or =6%) sequence variations. None of these had any association with late onset AD. This would suggest that polymorphic variations in the coding sequences of DVL1 are not important in AD. However further analysis of regulatory regions may lead to the identification of other sequence variations which may be implicated in AD.

摘要

阿尔茨海默病(AD)是一种以记忆力和其他认知功能进行性衰退为特征的疾病。神经原纤维缠结(NFT)是AD的主要病理标志,这些缠结是由高度磷酸化的微管相关蛋白tau组成的双螺旋丝(PHF)的聚集体。几种激酶,如糖原合酶激酶3β(GSK3β)和c-Jun氨基末端激酶(JNK),在PHF中磷酸化的位点使tau磷酸化。散乱蛋白1(DVL1)被认为是Wnt信号通路的正向调节因子,并抑制GSK3β活性,阻止β-连环蛋白降解,从而使Wnt靶基因得以表达。JNK的激活也受DVL1调节,然而尚不清楚这是否通过Wnt信号通路。这些观察结果表明DVL1在tau磷酸化和AD中起核心作用,并促使我们将DVL1作为该疾病的候选基因进行研究。我们通过测序和数据挖掘确定了DVL1基因的基因组结构,并在编码序列和侧翼内含子中寻找序列变异。DVL1基因跨越约13.8 kb的区域(不包括5'非翻译区),由15个外显子编码。对超过4.3 kb的序列进行分析,包括98%的外显子序列以及内含子2、3、6、7、9、10、11和12,发现有六个罕见(≤6%)的序列变异。这些变异均与晚发性AD无关联。这表明DVL1编码序列中的多态性变异在AD中并不重要。然而,对调控区域的进一步分析可能会导致发现其他可能与AD相关的序列变异。

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