Camarena Vladimir, Wang Gaofeng
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.
Bascom Palmer Eye Institute, University of Miami Miller School of Medicine, Miami, FL, 33136, USA.
Cell Mol Life Sci. 2016 Apr;73(8):1645-58. doi: 10.1007/s00018-016-2145-x. Epub 2016 Feb 4.
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.
最近的研究进展揭示了维生素C在表观遗传调控中一种前所未知的功能。在生理pH条件下,维生素C主要以抗坏血酸阴离子的形式存在。抗坏血酸被发现是负责DNA去甲基化的甲基胞嘧啶双加氧酶的辅因子,也是一些催化组蛋白去甲基化的含JmjC结构域的组蛋白去甲基酶的可能辅因子。因此,抗坏血酸生物利用度的变化会影响DNA和组蛋白的去甲基化,进而导致不同的表型表现。抗坏血酸缺乏可在发育和衰老的不同阶段,在不同组织中呈现系统性、空间性和时间性的表现。在此,我们综述抗坏血酸缺乏如何可能参与胚胎和出生后的发育,并通过表观遗传失调在神经退行性变和癌症等各种疾病中发挥作用。