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双加氧酶逆转碱基甲基化。

Reversal of nucleobase methylation by dioxygenases.

机构信息

Laboratory of Medical Epigenetics, Institutes of Biomedical Sciences, Medical College of Fudan University & Chinese Academy of Medical Sciences, Shanghai, China.

State Key Laboratory of Molecular Biology, Institute of Biochemistry and Cell Biology, Center for Excellence in Molecular Cell Science, Chinese Academy of Sciences, Shanghai, China.

出版信息

Nat Chem Biol. 2020 Nov;16(11):1160-1169. doi: 10.1038/s41589-020-00675-5. Epub 2020 Oct 16.

Abstract

The repertoire of nucleobase methylation in DNA and RNA, introduced by chemical agents or enzymes, is large. Most methylation can be reversed either directly by restoration of the original nucleobase or indirectly by replacement of the methylated nucleobase with an unmodified nucleobase. In many direct and indirect demethylation reactions, ALKBH (AlkB homolog) and TET (ten eleven translocation) hydroxylases play a role. Here, we suggest a chemical classification of methylation types. We then discuss pathways for removal, emphasizing oxidation reactions. We highlight the recently expanded repertoire of ALKBH- and TET-catalyzed reactions and describe the discovery of a TET-like protein that resembles the hydroxylases but uses an alternative co-factor and catalyzes glyceryl transfer rather than hydroxylation.

摘要

DNA 和 RNA 中的核碱基甲基化由化学试剂或酶引入,其类型繁多。大多数甲基化可通过原始核碱基的恢复直接逆转,或通过用未修饰的核碱基替换甲基化核碱基间接逆转。在许多直接和间接的去甲基化反应中,ALKBH(AlkB 同源物)和 TET(ten eleven translocation)羟化酶发挥作用。在这里,我们建议对甲基化类型进行化学分类。然后我们讨论了去除途径,强调氧化反应。我们重点介绍了最近扩展的 ALKBH 和 TET 催化反应谱,并描述了一种类似于羟化酶的 TET 样蛋白的发现,但它使用替代辅因子并催化甘油基转移而不是羟化。

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