TET enzymes, TDG and the dynamics of DNA demethylation

被引:0
|
作者
Rahul M. Kohli
Yi Zhang
机构
[1] Raymond and Ruth Perelman School of Medicine,Department of Medicine
[2] University of Pennsylvania,Department of Biochemistry and Biophysics
[3] Raymond and Ruth Perelman School of Medicine,Division of Hematology/Oncology, Department of Pediatrics
[4] University of Pennsylvania,Department of Genetics
[5] Howard Hughes Medical Institute,undefined
[6] WAB-1496,undefined
[7] 200 Longwood Ave.,undefined
[8] Program in Cellular and Molecular Medicine,undefined
[9] Boston Children's Hospital,undefined
[10] Boston Children's Hospital,undefined
[11] Harvard Medical School,undefined
[12] Harvard Stem Cell Institute,undefined
[13] 200 Longwood Ave.,undefined
来源
Nature | 2013年 / 502卷
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摘要
DNA methylation has a profound impact on genome stability, transcription and development. Although enzymes that catalyse DNA methylation have been well characterized, those that are involved in methyl group removal have remained elusive, until recently. The transformative discovery that ten-eleven translocation (TET) family enzymes can oxidize 5-methylcytosine has greatly advanced our understanding of DNA demethylation. 5-Hydroxymethylcytosine is a key nexus in demethylation that can either be passively depleted through DNA replication or actively reverted to cytosine through iterative oxidation and thymine DNA glycosylase (TDG)-mediated base excision repair. Methylation, oxidation and repair now offer a model for a complete cycle of dynamic cytosine modification, with mounting evidence for its significance in the biological processes known to involve active demethylation.
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页码:472 / 479
页数:7
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