4.6 Article

Genetic Effects on DNA Methylation and Its Potential Relevance for Obesity in Mexican Americans

期刊

PLOS ONE
卷 8, 期 9, 页码 -

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PUBLIC LIBRARY SCIENCE
DOI: 10.1371/journal.pone.0073950

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资金

  1. SEMP RUSS fund of the San Antonio Area Foundation
  2. NIDDK [DK087749]
  3. NIMH [MH0708143, MH078111, MH083824, MH59490]
  4. NHLBI [HL045522]
  5. Research Facilities Improvement Program from the National Center for Research Resources, National Institutes of Health [C06 RR017515]

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Several studies have identified effects of genetic variation on DNA methylation patterns and associated heritability, with research primarily focused on Caucasian individuals. In this paper, we examine the evidence for genetic effects on DNA methylation in a Mexican American cohort, a population burdened by a high prevalence of obesity. Using an Illumina-based platform and following stringent quality control procedures, we assessed a total of 395 CpG sites in peripheral blood samples obtained from 183 Mexican American individuals for evidence of heritability, proximal genetic regulation and association with age, sex and obesity measures (i.e. waist circumference and body mass index). We identified 16 CpG sites (similar to 4%) that were significantly heritable after Bonferroni correction for multiple testing and 27 CpG sites (similar to 6.9%) that showed evidence of genetic effects. Six CpG sites (similar to 2%) were associated with age, primarily exhibiting positive relationships, including CpG sites in two genes that have been implicated in previous genome-wide methylation studies of age (FZD9 and MYOD1). In addition, we identified significant associations between three CpG sites (similar to 1%) and sex, including DNA methylation in CASP6, a gene that may respond to estradiol treatment, and in HSD17B12, which encodes a sex steroid hormone. Although we did not identify any significant associations between DNA methylation and the obesity measures, several nominally significant results were observed in genes related to adipogenesis, obesity, energy homeostasis and glucose homeostasis (ARHGAP9, CDKN2A, FRZB, HOXA5, JAK3, MEST, NPY, PEG3 and SMARCB1). In conclusion, we were able to replicate several findings from previous studies in our Mexican American cohort, supporting an important role for genetic effects on DNA methylation. In addition, we found a significant influence of age and sex on DNA methylation, and report on trend-level, novel associations between DNA methylation and measures of obesity.

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