Volberg Vitaly, Yousefi Paul, Huen Karen, Harley Kim, Eskenazi Brenda, Holland Nina
Center for Environmental Research and Children's Health (CERCH), School of Public Health, University of California, 733 University Hall, Berkeley, CA, 94720-7360, USA.
BMC Med Genet. 2017 Jan 26;18(1):7. doi: 10.1186/s12881-016-0365-4.
To examine methylation of the peroxisome proliferator-activated receptor γ (PPARγ) gene and its relationship with child weight status, at birth and 9 years.
We measured PPARγ methylation across 23 CpG sites using the Infinium Illumina 450 k array for children from the Center for the Health Assessment of Mothers and Children of Salinas (CHAMACOS) cohort at birth (N = 373) and 9 years (N = 245).
Methylation level correlation patterns across the 23 PPARγ CpG sites were conserved between birth and 9-year ages. We found high inter-CpG correlations between sites 1-3 (methylation block 1) and also between sites 18-23 (methylation block 2) for both time points, although these patterns were less pronounced at 9 years. Additionally, sites 1-3 (north shore) had the highest intra-CpG correlations over time (r = 0.24, 0.42, and 0.3; P = 0.002, P < 0.001, P < 0.001, respectively). PPARγ methylation levels tended to increase with age, and the largest differences were observed for north shore sites (7.4%). Adjusting for sex, both site 1 and site 20 (gene body) methylation at birth was significantly and inversely associated with birth weight (β = -0.13, P = 0.033; β = -0.09, P = 0.025, respectively). Similarly, we found that site 1 and site 20 methylation at 9 years was significantly and inversely associated with 9-year BMI z-score (β = -0.41, P = 0.015; β = -0.23, P = 0.045, respectively).
Our results indicate that PPARγ methylation is highly organized and conserved over time, and highlight the potential functional importance of north shore sites, adding to a better understanding of regional human methylome patterns. Overall, our results suggest that PPARγ methylation may be associated with child body size.
研究过氧化物酶体增殖物激活受体γ(PPARγ)基因的甲基化及其与儿童出生时和9岁时体重状况的关系。
我们使用Illumina 450k芯片,对萨利纳斯母婴健康评估中心(CHAMACOS)队列中的儿童在出生时(N = 373)和9岁时(N = 245)的23个CpG位点进行了PPARγ甲基化检测。
23个PPARγ CpG位点的甲基化水平相关模式在出生时和9岁时是保守的。我们发现两个时间点的第1 - 3位点(甲基化区域1)之间以及第18 - 23位点(甲基化区域2)之间存在较高的CpG间相关性,尽管这些模式在9岁时不太明显。此外,第1 - 3位点(北岸)随时间的CpG内相关性最高(r分别为0.24、0.42和0.3;P分别为0.002、P < 0.001、P < 0.001)。PPARγ甲基化水平随年龄增长而升高,北岸位点的差异最大(7.4%)。校正性别后,出生时第1位点和第20位点(基因体)的甲基化与出生体重显著负相关(β分别为 - 0.13,P = 0.033;β为 - 0.09,P = 0.025)。同样,我们发现9岁时第1位点和第20位点的甲基化与9岁时的BMI z评分显著负相关(β分别为 - 0.41,P = 0.015;β为 - 0.23,P = 0.045)。
我们的结果表明,PPARγ甲基化随时间高度有序且保守,并突出了北岸位点的潜在功能重要性,有助于更好地理解区域人类甲基化组模式。总体而言,我们的结果表明PPARγ甲基化可能与儿童体型有关。