Skewed X-chromosome inactivation and XIST locus methylation levels do not contribute to the lower prevalence of Parkinson's disease in females

被引:11
作者
Sharma, Amit [1 ,2 ]
Kaut, Oliver [1 ]
Pavlova, Anna [2 ]
Froehlich, Holger [3 ,4 ]
Ahmad, Ashar [3 ]
Schmitt, Ina [1 ]
El-Maarri, Osman [5 ]
Oldenburg, Johannes [2 ]
Wuellner, Ullrich [1 ,6 ]
机构
[1] Univ Clin Bonn, Dept Neurol, Bonn, Germany
[2] Inst Expt Hematol & Transfus Med, Bonn, Germany
[3] Bonn Aachen Int Ctr IT B IT, Bonn, Germany
[4] UCB Biosci GmbH, Monheim, Germany
[5] Lebanese Amer Univ, Dept Nat Sci, Beirut, Lebanon
[6] German Ctr Neurodegenerat Dis DZNE, Bonn, Germany
关键词
Parkinson's disease; X inactivation; XIST; DNA methylation; GENE-EXPRESSION; HIGH-FREQUENCY; BLOOD-CELLS; WOMEN; RISK; PATTERNS; CARRIERS; DNA;
D O I
10.1016/j.neurobiolaging.2017.05.021
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Parkinson's disease (PD) is a degenerative disorder of the nervous system and the cause of the majority of sporadic cases is unknown. Females are relatively protected from PD as compared with males and linkage studies suggested a PD susceptibility locus on the X chromosome. To determine a putative association of skewed X-chromosome inactivation (XCI) and PD, we examined XCI patterns using a human androgen receptor geneebased assay (HUMARA) and did not identify any association of skewed or random X inactivation with clinical heterogeneity among female PD patients. In addition, we sought to determine methylation-specific changes at the X-inactive specific transcript (XIST) locus, which is known to be responsible for initiating X inactivation. We observed a trend towards hypomethylation in the gene body region of the XIST locus in PD females which did not reach significance. Furthermore, we extended our analysis of DNA methylation across the entire X-chromosome which revealed no methylation-specific differences between PD females and healthy controls. Thus, we propose that skewed XCI and methylation levels on the entire X chromosome did not reveal changes which could account for the decreased PD susceptibility in females or suitable to use as a biomarker. (C) 2017 Elsevier Inc. All rights reserved.
引用
收藏
页码:248.e1 / 248.e5
页数:5
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