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筛查南非帕金森病患者 DJ-1 基因 5'UTR 中的两个插入/缺失多态性。

Screening of two indel polymorphisms in the 5'UTR of the DJ-1 gene in South African Parkinson's disease patients.

机构信息

Division of Molecular Biology and Human Genetics, Faculty of Medicine and Health Sciences, Stellenbosch University, Tygerberg, P.O. Box 19063, Cape Town, 7505, South Africa,

出版信息

J Neural Transm (Vienna). 2014 Feb;121(2):135-8. doi: 10.1007/s00702-013-1094-x. Epub 2013 Sep 20.

Abstract

Mutations in the DJ-1 gene have been implicated in early-onset Parkinson's disease (PD). Two indel variants (g.168_185del and g.-6_+10del) in the 5'UTR of DJ-1 have been described. Genotyping of both variants in 402 South African PD patients of various ethnicities and 528 ethnically matched controls revealed that they are rare in the South African population. Further studies on these variants in other populations are warranted given their possible role in transcriptional regulation and DJ-1's critical role in alleviating oxidative stress.

摘要

DJ-1 基因突变与早发性帕金森病(PD)有关。DJ-1 5'UTR 中已有两种缺失变异(g.168_185del 和 g.-6_+10del)被描述。对来自不同种族的 402 名南非 PD 患者和 528 名种族匹配的对照者进行这两种变异的基因分型显示,它们在南非人群中很少见。鉴于这些变异可能在转录调控中发挥作用,以及 DJ-1 在缓解氧化应激方面的关键作用,有必要在其他人群中进一步研究这些变异。

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