Tet-Mediated Formation of 5-Hydroxymethylcytosine in RNA
Author(s) -
Lijuan Fu,
Candace R. Guerrero,
Na Zhong,
Nicholas J. Amato,
Yunhua Liu,
Shuo Liu,
Qian Cai,
Debin Ji,
SeungGi Jin,
Laura J. Niedernhofer,
Gerd P. Pfeifer,
Guo-Liang Xu,
Yinsheng Wang
Publication year - 2014
Publication title -
journal of the american chemical society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.115
H-Index - 612
eISSN - 1520-5126
pISSN - 0002-7863
DOI - 10.1021/ja505305z
Subject(s) - 5 hydroxymethylcytosine , chemistry , rna , enzyme , epigenetics , dna , in vitro , biochemistry , messenger rna , chromosomal translocation , 5 methylcytosine , dna methylation , gene , gene expression
Oxidation of 5-methylcytosine in DNA by ten-eleven translocation (Tet) family of enzymes has been demonstrated to play a significant role in epigenetic regulation in mammals. We found that Tet enzymes also possess the activity of catalyzing the formation of 5-hydroxymethylcytidine (5-hmrC) in RNA in vitro. In addition, the catalytic domains of all three Tet enzymes as well as full-length Tet3 could induce the formation of 5-hmrC in human cells. Moreover, 5-hmrC was present at appreciable levels (∼1 per 5000 5-methylcytidine) in RNA of mammalian cells and tissues. Our results suggest the involvement of this oxidation in RNA biology.
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