Research Paper
Individual variation and longitudinal pattern of genome-wide DNA methylation from birth to the first two years of life
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Volume 7, Issue 6 June 2012
Pages 594 - 605
http://dx.doi.org/10.4161/epi.20117
Keywords: CpG, DIP test, DNA Methylation, empirical bayes, genome-wide, normal mixture
Authors: Deli Wang, Xin Liu, Ying Zhou, Hehuang Xie, Xiumei Hong, Hui-Ju Tsai, Guoying Wang, Rong Liu and Xiaobin Wang
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- Deli Wang
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Corresponding author: wangdeli@gmail.com
Department of Psychiatry and Behavioral Sciences; Northwestern University Feinberg School of Medicine; Chicago, IL USA
These authors contributed equally to this work.
- Xin Liu
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Corresponding author: xnliu@childrensmemorial.org
The Mary Ann & J. Milburn Smith Child Health Research Program; Children’s Memorial Research Center/Children’s Memorial Hospital; Chicago, IL USA; Department of Pediatrics; Northwestern University Feinberg School of Medicine; Chicago, IL USA
These authors contributed equally to this work.
- Ying Zhou
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Biostatistics Research Core; Children’s Memorial Research Center/Children’s Memorial Hospital; Chicago, IL USA
- Hehuang Xie
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Cancer Biology and Epigenomics Program; Children’s Memorial Research Center/Children’s Memorial Hospital; Chicago, IL USA; Department of Pediatrics; Northwestern University Feinberg School of Medicine; Chicago, IL USA
- Xiumei Hong
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The Mary Ann & J. Milburn Smith Child Health Research Program; Children’s Memorial Research Center/Children’s Memorial Hospital; Chicago, IL USA; Department of Pediatrics; Northwestern University Feinberg School of Medicine; Chicago, IL USA
- Hui-Ju Tsai
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The Mary Ann & J. Milburn Smith Child Health Research Program; Children’s Memorial Research Center/Children’s Memorial Hospital; Chicago, IL USA; Department of Pediatrics; Northwestern University Feinberg School of Medicine; Chicago, IL USA; Division of Biostatistics and Bioinformatics; Institute of Population Health Sciences; National Health Research Institutes; Zhunan, Taiwan
- Guoying Wang
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The Mary Ann & J. Milburn Smith Child Health Research Program; Children’s Memorial Research Center/Children’s Memorial Hospital; Chicago, IL USA
- Rong Liu
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The Mary Ann & J. Milburn Smith Child Health Research Program; Children’s Memorial Research Center/Children’s Memorial Hospital; Chicago, IL USA
- Xiaobin Wang
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The Mary Ann & J. Milburn Smith Child Health Research Program; Children’s Memorial Research Center/Children’s Memorial Hospital; Chicago, IL USA; Department of Pediatrics; Northwestern University Feinberg School of Medicine; Chicago, IL USA; Center on Childhood Origins of Disease; Department of Population, Family and Reproductive Health; Johns Hopkins Bloomberg School of Public Health; Baltimore, MD USA
Abstract:
Prenatal development and early childhood are critical periods for establishing the tissue-specific epigenome, and may have a profound impact on health and disease in later life. However, epigenomic profiles at birth and in early childhood remain largely unexplored. The focus of this report is to examine the individual variation and longitudinal pattern of genome-wide DNA methylation levels from birth through the first two years of life in 105 Black children (59 males and 46 females) enrolled at the Boston Medical Center. We performed epigenomic mapping of cord blood at birth and venous blood samples from the same set of children within the first two years of life using Illumina Infinium Humanmethylation27 BeadChip. We observed a wide range of inter-individual variations in genome-wide methylation at each time point including lower levels at CpG islands, TSS200, 5′UTR and 1st Exon locations, but significantly higher levels in CpG shores, shelves, TSS1500, gene body and 3′UTR. We identified CpG sites with significant intra-individual longitudinal changes in the first two years of life throughout the genome. Specifically, we identified 159 CpG sites in males and 149 CpG sites in females with significant longitudinal changes defined by both statistical significance and magnitude of changes. These significant CpG sites appeared to be located within genes with important biological functions including immunity and inflammation. Further studies are needed to replicate our findings, including analysis by specific cell types, and link those individual variations and longitudinal changes with specific health outcomes in early childhood and later life.
Received: December 17, 2011; Accepted: March 22, 2012; Published Online: June 1, 2012
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