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Reversal of nucleobase methylation by dioxygenases.
Xu, Guo-Liang; Bochtler, Matthias.
Afiliación
  • Xu GL; Laboratory of Medical Epigenetics, Institutes of Biomedical Sciences, Medical College of Fudan University & Chinese Academy of Medical Sciences, Shanghai, China. glxu@sibcb.ac.cn.
  • Bochtler M; 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. glxu@sibcb.ac.cn.
Nat Chem Biol ; 16(11): 1160-1169, 2020 11.
Article en En | MEDLINE | ID: mdl-33067602
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.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: ADN / ARN / Dioxigenasas / Proteínas de Unión al ADN Límite: Humans Idioma: En Revista: Nat Chem Biol Asunto de la revista: BIOLOGIA / QUIMICA Año: 2020 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: ADN / ARN / Dioxigenasas / Proteínas de Unión al ADN Límite: Humans Idioma: En Revista: Nat Chem Biol Asunto de la revista: BIOLOGIA / QUIMICA Año: 2020 Tipo del documento: Article País de afiliación: China