重编程
DNA去甲基化
表观遗传学
DNA甲基化
生物
抗坏血酸
体细胞
组蛋白
脱甲基酶
甲基化
细胞生物学
遗传学
生物化学
DNA
细胞
基因表达
基因
食品科学
作者
Xinhui Liu,Aamir Ali Khan,Huan Li,Shensen Wang,Xuechai Chen,Hua Huang
出处
期刊:Current stem cell research & therapy
[Bentham Science]
日期:2022-01-01
卷期号:17 (1): 13-25
被引量:9
标识
DOI:10.2174/1574888x16666210714152730
摘要
: 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
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