SNCA基因甲基化在帕金森病和多系统萎缩中的作用

IF 2.5 Q3 GENETICS & HEREDITY
Ekaterina Yu Fedotova, Elena V Iakovenko, Natalia Yu Abramycheva, Sergey N Illarioshkin
{"title":"SNCA基因甲基化在帕金森病和多系统萎缩中的作用","authors":"Ekaterina Yu Fedotova,&nbsp;Elena V Iakovenko,&nbsp;Natalia Yu Abramycheva,&nbsp;Sergey N Illarioshkin","doi":"10.3390/epigenomes7010005","DOIUrl":null,"url":null,"abstract":"<p><p>In recent years, epigenetic mechanisms have been implicated in the development of multifactorial diseases including neurodegenerative disorders. In Parkinson's disease (PD), as a synucleinopathy, most studies focused on DNA methylation of <i>SNCA</i> gene coding alpha-synuclein but obtained results were rather contradictory. In another neurodegenerative synucleinopathy, multiple system atrophy (MSA), very few studies investigated the epigenetic regulation. This study included patients with PD (n = 82), patients with MSA (n = 24), and a control group (n = 50). In three groups, methylation levels of CpG and non-CpG sites in regulatory regions of the <i>SNCA</i> gene were analyzed. We revealed hypomethylation of CpG sites in the <i>SNCA</i> intron 1 in PD and hypermethylation of predominantly non-CpG sites in the <i>SNCA</i> promoter region in MSA. In PD patients, hypomethylation in the intron 1 was associated with earlier age at the disease onset. In MSA patients, hypermethylation in the promotor was associated with shorter disease duration (before examination). These results showed different patterns of the epigenetic regulation in two synucleinopathies-PD and MSA.</p>","PeriodicalId":55768,"journal":{"name":"Epigenomes","volume":"7 1","pages":""},"PeriodicalIF":2.5000,"publicationDate":"2023-02-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9944792/pdf/","citationCount":"1","resultStr":"{\"title\":\"<i>SNCA</i> Gene Methylation in Parkinson's Disease and Multiple System Atrophy.\",\"authors\":\"Ekaterina Yu Fedotova,&nbsp;Elena V Iakovenko,&nbsp;Natalia Yu Abramycheva,&nbsp;Sergey N Illarioshkin\",\"doi\":\"10.3390/epigenomes7010005\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>In recent years, epigenetic mechanisms have been implicated in the development of multifactorial diseases including neurodegenerative disorders. In Parkinson's disease (PD), as a synucleinopathy, most studies focused on DNA methylation of <i>SNCA</i> gene coding alpha-synuclein but obtained results were rather contradictory. In another neurodegenerative synucleinopathy, multiple system atrophy (MSA), very few studies investigated the epigenetic regulation. This study included patients with PD (n = 82), patients with MSA (n = 24), and a control group (n = 50). In three groups, methylation levels of CpG and non-CpG sites in regulatory regions of the <i>SNCA</i> gene were analyzed. We revealed hypomethylation of CpG sites in the <i>SNCA</i> intron 1 in PD and hypermethylation of predominantly non-CpG sites in the <i>SNCA</i> promoter region in MSA. In PD patients, hypomethylation in the intron 1 was associated with earlier age at the disease onset. In MSA patients, hypermethylation in the promotor was associated with shorter disease duration (before examination). These results showed different patterns of the epigenetic regulation in two synucleinopathies-PD and MSA.</p>\",\"PeriodicalId\":55768,\"journal\":{\"name\":\"Epigenomes\",\"volume\":\"7 1\",\"pages\":\"\"},\"PeriodicalIF\":2.5000,\"publicationDate\":\"2023-02-06\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9944792/pdf/\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Epigenomes\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.3390/epigenomes7010005\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"GENETICS & HEREDITY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Epigenomes","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3390/epigenomes7010005","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"GENETICS & HEREDITY","Score":null,"Total":0}
引用次数: 1

摘要

近年来,表观遗传机制已涉及多因素疾病的发展,包括神经退行性疾病。在帕金森病(PD)中,作为一种突触核蛋白病,大多数研究都集中在编码α -突触核蛋白的SNCA基因的DNA甲基化上,但得到的结果却相当矛盾。在另一种神经退行性突触核蛋白病,多系统萎缩(MSA)中,很少有研究研究表观遗传调控。本研究包括PD患者(n = 82)、MSA患者(n = 24)和对照组(n = 50)。在三组中,分析SNCA基因调控区域CpG和非CpG位点的甲基化水平。我们发现PD中SNCA内含子1中CpG位点的低甲基化和MSA中SNCA启动子区域主要非CpG位点的高甲基化。在PD患者中,内含子1的低甲基化与疾病发病年龄较早有关。在MSA患者中,启动子的高甲基化与较短的疾病持续时间(检查前)相关。这些结果表明pd和MSA两种突触核蛋白病的表观遗传调控模式不同。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

<i>SNCA</i> Gene Methylation in Parkinson's Disease and Multiple System Atrophy.

<i>SNCA</i> Gene Methylation in Parkinson's Disease and Multiple System Atrophy.

<i>SNCA</i> Gene Methylation in Parkinson's Disease and Multiple System Atrophy.

SNCA Gene Methylation in Parkinson's Disease and Multiple System Atrophy.

In recent years, epigenetic mechanisms have been implicated in the development of multifactorial diseases including neurodegenerative disorders. In Parkinson's disease (PD), as a synucleinopathy, most studies focused on DNA methylation of SNCA gene coding alpha-synuclein but obtained results were rather contradictory. In another neurodegenerative synucleinopathy, multiple system atrophy (MSA), very few studies investigated the epigenetic regulation. This study included patients with PD (n = 82), patients with MSA (n = 24), and a control group (n = 50). In three groups, methylation levels of CpG and non-CpG sites in regulatory regions of the SNCA gene were analyzed. We revealed hypomethylation of CpG sites in the SNCA intron 1 in PD and hypermethylation of predominantly non-CpG sites in the SNCA promoter region in MSA. In PD patients, hypomethylation in the intron 1 was associated with earlier age at the disease onset. In MSA patients, hypermethylation in the promotor was associated with shorter disease duration (before examination). These results showed different patterns of the epigenetic regulation in two synucleinopathies-PD and MSA.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Epigenomes
Epigenomes GENETICS & HEREDITY-
CiteScore
3.80
自引率
0.00%
发文量
38
审稿时长
11 weeks
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信