5-Hydroxymethyl-, 5-Formyl- and 5-Carboxydeoxycytidines as Oxidative Lesions and Epigenetic Marks

被引:6
作者
Schelter, Florian [1 ]
Kirchner, Angie [1 ,2 ]
Traube, Franziska R. [1 ]
Mueller, Markus [1 ]
Steglich, Wolfgang [1 ]
Carell, Thomas [1 ]
机构
[1] Ludwigs Maximilian Univ Munchen, Butenandtstr 5-13, D-81377 Munich, Germany
[2] Univ Cambridge, Canc Res UK Cambridge Inst, Li Ka Shing Ctr, Cambridge CB2 0RE, England
基金
欧洲研究理事会;
关键词
DNA repair; DNA modification; epigenetics; mass spectrometry; oxidative lesion; THYMINE DNA GLYCOSYLASE; BASE; 5-CARBOXYLCYTOSINE; DEMETHYLATION; METHYLATION; EXCISION; 5-METHYLCYTOSINE; REVEALS; GENES; COULD;
D O I
10.1002/chem.202100551
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The four non-canonical nucleotides in the human genome 5-methyl-, 5-hydroxymethyl-, 5-formyl- and 5-carboxydeoxycytidine (mdC, hmdC, fdC and cadC) form a second layer of epigenetic information that contributes to the regulation of gene expression. Formation of the oxidized nucleotides hmdC, fdC and cadC requires oxidation of mdC by ten-eleven translocation (Tet) enzymes that require oxygen, Fe(II) and alpha-ketoglutarate as cosubstrates. Although these oxidized forms of mdC are widespread in mammalian genomes, experimental evidence for their presence in fungi and plants is ambiguous. This vagueness is caused by the fact that these oxidized mdC derivatives are also formed as oxidative lesions, resulting in unclear basal levels that are likely to have no epigenetic function. Here, we report the xdC levels in the fungus Amanita muscaria in comparison to murine embryonic stem cells (mESCs), HEK cells and induced pluripotent stem cells (iPSCs), to obtain information about the basal levels of hmdC, fdC and cadC as DNA lesions in the genome.
引用
收藏
页码:8100 / 8104
页数:5
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