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    Patterns of DNA methylation across the leptin core promoter in four diverse Asian and north American populations

    Access Status
    Fulltext not available
    Authors
    Mosher, M.
    Melton, Phillip
    Stapleton, P.
    Schanfield, M.
    Crawford, M.
    Date
    2017
    Type
    Journal Article
    
    Metadata
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    Citation
    Mosher, M. and Melton, P. and Stapleton, P. and Schanfield, M. and Crawford, M. 2017. Patterns of DNA methylation across the leptin core promoter in four diverse Asian and north American populations. Human Biology. 88 (2): pp. 121-135.
    Source Title
    Human Biology
    ISSN
    0018-7143
    School
    School of Biomedical Sciences
    URI
    http://hdl.handle.net/20.500.11937/57984
    Collection
    • Curtin Research Publications
    Abstract

    © 2017 Wayne State University Press. DNA methylation is the most widely studied of epigenetic mechanisms, with environmental effects recorded through patterned attachments of methyl groups along the DNA that are capable of modifying gene expression without altering the DNA sequencing. The degree to which these patterns of DNA methylation are heritable, the expected range of normality across populations, and the phenotypic relevance of pattern variation remain unclear. Genes regulating metabolic pathways appear to be vulnerable to ongoing nutritional programming over the life course, as dietary nutrients are significant environmental determinants of DNA methylation, supplying both the methyl groups and energy to generate the methylation process. Here we examine methylation patterns along a region of the metabolic gene leptin (LEP). LEP’s putative functions include regulation of energy homeostasis, with its signals affecting energy intake and expenditure, adipogenesis and energy storage, lipid and glucose metabolism, bone metabolism, and reproductive endocrine function. A pattern of differential methylation across CpG sites of the LEP core promoter has been previously identified; however, any consistency of pattern or its phenotypic significance is not fully elucidated among populations. Using DNA extracted from unfractionated white blood cells of peripheral blood samples, our pilot study, divided into two parts, examined the significance of variation in DNA methylation patterns along the leptin core promoter in four populations (phase 1) and used biomarkers reflecting leptin’s functional process in two of those populations, western Buryat of Siberia and the Mennonite of central Kansas, to investigate the relevance of the ethnic variation identified in the DNA methylation (phase 2). LEP’s core promoter region contains both the binding site for C/EBPa (CCAAT/enhancer binding protein alpha), which tempers the final step in adipocyte maturity and capacity to synthesize leptin, and the TATA motif controlling leptin synthesis. Previous studies report that increased methylation in this region is correlated to decreased gene expression, suggesting tissue-specific methylation variation at this region (Melzner et al. 2002). We hypothesized that evidence of nutritional epigenetic programming would be identified through variation in patterns of DNA methylation and that functional relevance of that variation among populations would be identified through biomarkers that reflect leptin’s metabolic signals: serum leptin levels, lipoproteins of the lipid transport system, and anthropometric measures.

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