Integrative Co-methylation Network Analysis Identifies Novel DNA Methylation Signatures and Their Target Genes in Alzheimer?s Disease

被引:6
|
作者
Kim, Jun Pyo [1 ,2 ]
Kim, Bo-Hyun [3 ]
Bice, Paula J. [1 ,6 ]
Seo, Sang Won [4 ]
Bennett, David A. [5 ]
Saykin, Andrew J. [1 ,6 ,7 ]
Nho, Kwangsik [1 ,6 ,8 ]
机构
[1] Indiana Univ Sch Med, Ctr Neuroimaging Radiol & Imaging Sci, Indianapolis, IN 46202 USA
[2] Sungkyunkwan Univ, Med Res Inst, Sch Med, Seoul, South Korea
[3] Hanyang Univ, Dept Biomed Engn, Seoul, South Korea
[4] Sungkyunkwan Univ, Samsung Med Ctr, Sch Med, Dept Neurol, Seoul, South Korea
[5] Rush Univ, Rush Alzheimers Dis Ctr, Med Ctr, Chicago, IL USA
[6] Indiana Univ Sch Med, Indiana Alzheimers Dis Res Ctr, Indianapolis, IN USA
[7] Indiana Univ Sch Med, Dept Med & Mol Genet, Indianapolis, IN USA
[8] Indiana Univ Sch Med, Ctr Computat Biol & Bioinformat, Indian, IN USA
关键词
EPIGENOME-WIDE ASSOCIATION; RELIGIOUS ORDERS; OLDER PERSONS; RUSH MEMORY; A-BETA; BRAIN; SUSCEPTIBILITY; METAANALYSIS; HAPLOTYPE; LOCI;
D O I
10.1016/j.biopsych.2022.06.020
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
BACKGROUND: DNA methylation is a key epigenetic marker, and its alternations may be involved in Alzheimer's disease (AD). CpGs sharing similar biological functions or pathways tend to be co-methylated.METHODS: We performed an integrative network-based DNA methylation analysis on 2 independent cohorts (N = 941) using brain DNA methylation profiles and RNA-sequencing as well as AD pathology data.RESULTS: Weighted co-methylation network analysis identified 6 modules as significantly associated with neuritic plaque burden. In total, 15 hub CpGs including 3 novel CpGs were identified and replicated as being significantly associated with AD pathology. Furthermore, we identified and replicated 4 target genes (ATP6V1G2, VCP, RAD52, and LST1) as significantly regulated by DNA methylation at hub CpGs. In particular, VCP gene expression was also associated with AD pathology in both cohorts.CONCLUSIONS: This integrative network-based multiomics study provides compelling evidence for a potential role of DNA methylation alternations and their target genes in AD.
引用
收藏
页码:842 / 851
页数:10
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