Genome-wide analysis of aberrant methylation of enhancer DNA in human osteoarthritis

被引:22
|
作者
Li, Xiaozong [1 ]
Li, Li [2 ]
Li, Xiaojuan [3 ]
Tian, Jun [1 ]
Zheng, Weizhuo [1 ]
Li, Jin [4 ]
Wang, Limei [4 ,5 ]
机构
[1] Harbin Med Univ, Dept Orthoped, Affiliated Hosp 2, Harbin 150081, Peoples R China
[2] Harbin Med Univ, Dept Nucl Med, Affiliated Hosp, Harbin 150001, Peoples R China
[3] Harbin Med Univ, Dept Rehabil, Affiliated Hosp 1, Harbin 150001, Peoples R China
[4] Harbin Med Univ, Coll Bioinformat Sci & Technol, Harbin 150081, Peoples R China
[5] Harbin Engn Univ, Coll Automat, Harbin 150001, Peoples R China
基金
中国国家自然科学基金;
关键词
GENE; KNEE; IDENTIFICATION; CARTILAGE; REVEALS; EPIGENETICS; DISEASE; SEX; HIP;
D O I
10.1186/s12920-019-0646-9
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Background Osteoarthritis is a chronic musculoskeletal disease characterized by age-related gradual thinning and a high risk in females. Recent studies have shown that DNA methylation plays important roles in osteoarthritis. However, the genome-wide pattern of methylation in enhancers in osteoarthritis remains unclear. Methods To explore the function of enhancers in osteoarthritis, we quantified CpG methylation in human enhancers based on a public dataset that included methylation profiles of 470,870 CpG probes in 108 samples from patients with hip and knee osteoarthritis and hip tissues from healthy individuals. Combining various bioinformatics analysis tools, we systematically analyzed aberrant DNA methylation of the enhancers throughout the genome in knee osteoarthritis and hip osteoarthritis. Results We identified 16,816 differentially methylated CpGs, and nearly half (8111) of them were from enhancers, suggesting major DNA methylation changes in both types of osteoarthritis in the enhancer regions. A detailed analysis of hip osteoarthritis identified 2426 differentially methylated CpGs in enhancers between male and female patients, and 84.5% of them were hypomethylated in female patients and enriched in phenotypes related to hip osteoarthritis in females. Next, we explored the enhancer methylation dynamics among patients with knee osteoarthritis and identified 280 differentially methylated enhancer CpGs that were enriched in the human phenotypes and disease ontologies related to osteoarthritis. Finally, a comparison of enhancer methylation between knee osteoarthritis and hip osteoarthritis revealed organ source-dependent differences in enhancer methylation. Conclusion Our findings indicate that aberrant methylation of enhancers is related to osteoarthritis phenotypes, and a comprehensive atlas of enhancer methylation is useful for further analysis of the epigenetic regulation of osteoarthritis and the development of clinical drugs for treatment of osteoarthritis.
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页数:10
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