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抗坏血酸在表观遗传重编程中的作用。

Ascorbic Acid in Epigenetic Reprogramming.

机构信息

College of Life Science and Bioengineering, Beijing University of Technology, Beijing 100124, China.

出版信息

Curr Stem Cell Res Ther. 2022;17(1):13-25. doi: 10.2174/1574888X16666210714152730.

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.

摘要

新出现的证据表明,抗坏血酸(维生素 C)通过多种机制增强重编程过程,主要是由于其在 Fe(II)和 2-氧戊二酸依赖性双加氧酶中的辅助因子作用,包括 DNA 去甲基酶 Ten Eleven Translocase(TET)和组蛋白去甲基酶。表观遗传变异已被证明在体细胞重编程中起着关键作用。DNA 甲基化和组蛋白甲基化被广泛认为是体细胞重编程的障碍。N6-甲基腺苷(m6A),也称为 RNA 甲基化,是 mRNAs 的一种表观遗传修饰,也被证明在调节细胞重编程中发挥作用。有报道称,多种辅助因子可促进这些去甲基酶的活性,包括维生素 C。因此,本综述重点探讨和研究了维生素 C 在 DNA 和组蛋白去甲基化中的作用和机制,并强调了其在 m6A 去甲基化调节中的潜在作用。它还展示了维生素 C 在表观遗传调控中的重要贡献,以及去甲基酶与维生素 C 促进的表观遗传重编程的关联。

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