The epigenetic role of vitamin C in health and disease
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  • 作者:Vladimir Camarena ; Gaofeng Wang
  • 关键词:Epigenetics ; Vitamin C ; Methylcytosine dioxygenase ; DNA methylation ; JmjC domain ; containing histone demethylases ; Histone methylation ; Scurvy
  • 刊名:Cellular and Molecular Life Sciences (CMLS)
  • 出版年:2016
  • 出版时间:April 2016
  • 年:2016
  • 卷:73
  • 期:8
  • 页码:1645-1658
  • 全文大小:696 KB
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  • 作者单位:Vladimir Camarena (1)
    Gaofeng Wang (1) (2) (3)

    1. John P. Hussman Institute for Human Genomics, Dr. John T. Macdonald Foundation Department of Human Genetics, University of Miami Miller School of Medicine, Biomedical Research Building, Rm. 608, 1501 NW 10th Ave, Miami, FL, 33136, USA
    2. Bascom Palmer Eye Institute, University of Miami Miller School of Medicine, Miami, FL, 33136, USA
    3. Sylvester Comprehensive Cancer Center, University of Miami Miller School of Medicine, Miami, FL, 33136, USA
  • 刊物类别:Biomedical and Life Sciences
  • 刊物主题:Life Sciences
    Cell Biology
    Biomedicine
    Life Sciences
    Biochemistry
  • 出版者:Birkh盲user Basel
  • ISSN:1420-9071
文摘
Recent advances have uncovered a previously unknown function of vitamin C in epigenetic regulation. Vitamin C exists predominantly as an ascorbate anion under physiological pH conditions. Ascorbate was discovered as a cofactor for methylcytosine dioxygenases that are responsible for DNA demethylation, and also as a likely cofactor for some JmjC domain-containing histone demethylases that catalyze histone demethylation. Variation in ascorbate bioavailability thus can influence the demethylation of both DNA and histone, further leading to different phenotypic presentations. Ascorbate deficiency can be presented systematically, spatially and temporally in different tissues at the different stages of development and aging. Here, we review how ascorbate deficiency could potentially be involved in embryonic and postnatal development, and plays a role in various diseases such as neurodegeneration and cancer through epigenetic dysregulation.

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