Nilsson Emma, Jansson Per Anders, Perfilyev Alexander, Volkov Petr, Pedersen Maria, Svensson Maria K, Poulsen Pernille, Ribel-Madsen Rasmus, Pedersen Nancy L, Almgren Peter, Fadista João, Rönn Tina, Klarlund Pedersen Bente, Scheele Camilla, Vaag Allan, Ling Charlotte
Epigenetics and Diabetes, Department of Clinical Sciences, Lund University Diabetes Centre, Lund University, Clinical Research Centre, Malmö, Sweden Department of Endocrinology, Diabetes and Metabolism, Rigshospitalet, Copenhagen, Denmark
Wallenberg Laboratory, Sahlgrenska University Hospital, Gothenburg, Sweden.
Diabetes. 2014 Sep;63(9):2962-76. doi: 10.2337/db13-1459. Epub 2014 May 8.
Genetics, epigenetics, and environment may together affect the susceptibility for type 2 diabetes (T2D). Our aim was to dissect molecular mechanisms underlying T2D using genome-wide expression and DNA methylation data in adipose tissue from monozygotic twin pairs discordant for T2D and independent case-control cohorts. In adipose tissue from diabetic twins, we found decreased expression of genes involved in oxidative phosphorylation; carbohydrate, amino acid, and lipid metabolism; and increased expression of genes involved in inflammation and glycan degradation. The most differentially expressed genes included ELOVL6, GYS2, FADS1, SPP1 (OPN), CCL18, and IL1RN. We replicated these results in adipose tissue from an independent case-control cohort. Several candidate genes for obesity and T2D (e.g., IRS1 and VEGFA) were differentially expressed in discordant twins. We found a heritable contribution to the genome-wide DNA methylation variability in twins. Differences in methylation between monozygotic twin pairs discordant for T2D were subsequently modest. However, 15,627 sites, representing 7,046 genes including PPARG, KCNQ1, TCF7L2, and IRS1, showed differential DNA methylation in adipose tissue from unrelated subjects with T2D compared with control subjects. A total of 1,410 of these sites also showed differential DNA methylation in the twins discordant for T2D. For the differentially methylated sites, the heritability estimate was 0.28. We also identified copy number variants (CNVs) in monozygotic twin pairs discordant for T2D. Taken together, subjects with T2D exhibit multiple transcriptional and epigenetic changes in adipose tissue relevant to the development of the disease.
遗传学、表观遗传学和环境因素可能共同影响2型糖尿病(T2D)的易感性。我们的目标是利用来自T2D不一致的同卵双胞胎对以及独立病例对照队列的脂肪组织中的全基因组表达和DNA甲基化数据,剖析T2D潜在的分子机制。在糖尿病双胞胎的脂肪组织中,我们发现参与氧化磷酸化、碳水化合物、氨基酸和脂质代谢的基因表达降低,而参与炎症和聚糖降解的基因表达增加。差异表达最显著的基因包括ELOVL6、GYS2、FADS1、SPP1(骨桥蛋白)、CCL18和IL1RN。我们在一个独立病例对照队列的脂肪组织中重复了这些结果。肥胖和T2D的几个候选基因(如IRS1和VEGFA)在不一致的双胞胎中差异表达。我们发现双胞胎中全基因组DNA甲基化变异性存在遗传贡献。T2D不一致的同卵双胞胎对之间的甲基化差异随后较小。然而,15627个位点,代表7046个基因,包括PPARG、KCNQ1、TCF7L2和IRS1,在患有T2D的非亲属受试者与对照受试者的脂肪组织中显示出差异DNA甲基化。其中共有1410个位点在T2D不一致的双胞胎中也显示出差异DNA甲基化。对于差异甲基化位点,遗传度估计值为0.28。我们还在T2D不一致的同卵双胞胎对中鉴定出拷贝数变异(CNV)。综上所述,患有T2D的受试者在与疾病发展相关的脂肪组织中表现出多种转录和表观遗传变化。