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DESCRIPTION (provided by applicant): There is accumulating evidence that the pathogenesis of many adult-onset chronic diseases, including type 2 diabetes, cardiovascular disease, and cancer, can be influenced by nutrition in early life. One probable underlying mechanism is through early nutritional effects on epigenetics, i.e. self-perpetuating gene regulatory systems that are not dependent on DNA sequence. A particularly relevant epigenetic mechanism involves the methylation of cytosine residues on both strands of palindromic CpG dinucleotides. Mammalian one-carbon metabolism, which provides the methyl groups for biological methylation reactions, is highly dependent on dietary substrates and cofactors. Thus, the establishment and maintenance of genomic methylation patterns during early development may make it more critical to maintain appropriate levels of these diet-derived components at that time than during later life. The overall hypothesis of the proposed research is that maternal dietary methyl donor supplementation before conception and during pregnancy alters DNA methylation of specific genomic regions in the early embryo, and that these induced epigenetic alterations persist to adulthood. We propose to test this hypothesis in mouse models, focusing on two gene classes: genes adjacent to transposon elements, and genomically imprinted genes. Understanding the specific biologic mechanisms linking early nutrition to adult gene expression and metabolism may ultimately enable early-life nutritional interventions aimed at ameliorating adult-onset chronic disease in humans. This proposal describes a five-year training program for the development of an academic career in Nutrition and Developmental Genetics. The proposed research builds upon previous work by the principal investigator, and entails developing new approaches that will broaden his research capabilities. The applicant's long-term goals include building on this animal model research to develop specific hypotheses regarding early nutritional influences on epigenetic gene regulation in humans.
期刊论文(8)
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会议论文
Epigenetic epidemiology of obesity: application of epigenomic technology.
肥胖的表观遗传流行病学:表观基因组技术的应用。
DOI: 10.1111/j.1753-4887.2008.00060.x
发表时间: 2008
期刊: Nutrition reviews
影响因子: 6.1
作者: [Waterland,RobertA]
通讯作者: Waterland,RobertA
DOI: 10.1038/ijo.2008.100
发表时间: 2008-09
期刊: INTERNATIONAL JOURNAL OF OBESITY
影响因子: 4.9
作者: [Waterland, R. A., Travisano, M., Tahiliani, K. G., Rached, M. T., Mirza, S.]
通讯作者: Mirza, S.
DOI: 10.1159/000178030
发表时间: 2009-01-01
期刊: HORMONE RESEARCH
影响因子: --
作者: [Waterland, Robert A.]
通讯作者: Waterland, Robert A.
Systemic interindividual epigenetic variants in African Americans: Identification, characterization, and prospective associations with obesity
  • 批准号:
    10626106
  • 项目类别:
  • 资助金额:
    $56.21万
  • 财政年份:
    2021
  • 负责人:
    ROBERT A WATERLAND
  • 依托单位:
Systemic interindividual epigenetic variants in African Americans: Identification, characterization, and prospective associations with obesity
  • 批准号:
    10473790
  • 项目类别:
  • 资助金额:
    $58.14万
  • 财政年份:
    2021
  • 负责人:
    ROBERT A WATERLAND
  • 依托单位:
Systemic interindividual epigenetic variants in African Americans: Identification, characterization, and prospective associations with obesity
  • 批准号:
    10272655
  • 项目类别:
  • 资助金额:
    $51.96万
  • 财政年份:
    2021
  • 负责人:
    ROBERT A WATERLAND
  • 依托单位:
Unbiased identification and characterization of mouse metastable epialleles
  • 批准号:
    10190936
  • 项目类别:
  • 资助金额:
    $46.24万
  • 财政年份:
    2020
  • 负责人:
    ROBERT A WATERLAND
  • 依托单位:
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