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孕期DNA甲基化轨迹

DNA Methylation Trajectories During Pregnancy.

作者信息

Gruzieva Olena, Merid Simon Kebede, Chen Su, Mukherjee Nandini, Hedman Anna M, Almqvist Catarina, Andolf Ellika, Jiang Yu, Kere Juha, Scheynius Annika, Söderhäll Cilla, Ullemar Vilhelmina, Karmaus Wilfried, Melén Erik, Arshad Syed Hasan, Pershagen Göran

机构信息

Institute of Environmental Medicine, Karolinska Institutet, Stockholm, Sweden.

Centre for Occupational and Environmental Medicine, Stockholm County Council, Stockholm, Sweden.

出版信息

Epigenet Insights. 2019 Aug 13;12:2516865719867090. doi: 10.1177/2516865719867090. eCollection 2019.

Abstract

There is emerging evidence on DNA methylation (DNAm) variability over time; however, little is known about dynamics of DNAm patterns during pregnancy. We performed an epigenome-wide longitudinal DNAm study of a well-characterized sample of young women from the Swedish Born into Life study, with repeated blood sampling before, during and after pregnancy (n = 21), using the Illumina Infinium MethylationEPIC array. We conducted a replication in the Isle of Wight third-generation birth cohort (n = 27), using the Infinium HumanMethylation450k BeadChip. We identified 196 CpG sites displaying intra-individual longitudinal change in DNAm with a false discovery rate (FDR)  < .05. Most of these (91%) showed a decrease in average methylation levels over the studied period. We observed several genes represented by ⩾3 differentially methylated CpGs: , and MicroRNA 10a. Of 36 CpGs available in the replication cohort, 17 were replicated, all but 2 with the same direction of association (replication  < .05). Biological pathway analysis demonstrated that FDR-significant CpGs belong to genes overrepresented in metabolism-related pathways, such as adipose tissue development, regulation of insulin receptor signaling, and mammary gland fat development. These results contribute to a better understanding of the biological mechanisms underlying important physiological alterations and adaptations for pregnancy and lactation.

摘要

随着时间推移,有关DNA甲基化(DNAm)变异性的证据不断涌现;然而,关于孕期DNAm模式的动态变化却知之甚少。我们对瑞典“生命之初”研究中一组特征明确的年轻女性样本进行了全表观基因组纵向DNAm研究,在怀孕前、孕期和产后对她们进行多次血液采样(n = 21),使用Illumina Infinium MethylationEPIC芯片。我们在怀特岛第三代出生队列(n = 27)中进行了复制研究,使用Infinium HumanMethylation450k芯片。我们鉴定出196个CpG位点,其DNAm显示个体内纵向变化,错误发现率(FDR)<0.05。其中大部分(91%)在研究期间平均甲基化水平下降。我们观察到几个由≥3个差异甲基化CpG代表的基因:……以及MicroRNA 10a。在复制队列中可用的36个CpG中,有17个得到复制,除2个外,所有复制的关联方向相同(复制FDR<0.05)。生物学通路分析表明,FDR显著的CpG属于在代谢相关通路中过度表达的基因,如脂肪组织发育、胰岛素受体信号调节和乳腺脂肪发育。这些结果有助于更好地理解孕期和哺乳期重要生理改变及适应背后的生物学机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1f7e/6696836/e3585703d6f7/10.1177_2516865719867090-fig1.jpg

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