Affiliation:
1. College of Life Science and Bioengineering, Beijing University of Technology, Beijing 100124, China
Abstract
:
Emerging evidence suggests that ascorbic acid (vitamin C) enhances the reprogramming
process by multiple mechanisms primarily due to its cofactor role in Fe(II) and 2-oxoglutarate-dependent
dioxygenases, including the DNA demethylases Ten Eleven Translocase (TET) and histone
demethylases. Epigenetic variations have been shown to play a critical role in somatic cell reprogramming.
DNA methylation and histone methylation are extensively recognized as barriers to
somatic cell reprogramming. N6-methyladenosine (m6A), known as RNA methylation, is an epigenetic
modification of mRNAs and has also been shown to play a role in regulating cellular reprogramming.
Multiple cofactors are reported to promote the activity of these demethylases, including
vitamin C. Therefore, this review focuses and examines the evidence and mechanism of vitamin C
in DNA and histone demethylation and highlights its potential involvement in the regulation of
m6A demethylation. It also shows the significant contribution of vitamin C in epigenetic regulation,
and the affiliation of demethylases with vitamin C-facilitated epigenetic reprogramming.
• Introduction
• Vitamin C, DNA Demethylation, and Epigenetic Reprogramming
• Vitamin C, Histone demethylation, and Epigenetic Reprogramming
• Vitamin C, m6A RNA demethylation and Epigenetic Reprogramming
• Conclusion
Funder
National Natural Science Foundation of China
programs of the Beijing Municipal Commission of Education
Publisher
Bentham Science Publishers Ltd.
Subject
General Medicine,Medicine (miscellaneous)
Cited by
15 articles.
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