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PMID: 15040447 Published · ppublish English Journal Article Review

Repairing DNA-methylation damage.

Nature reviews. Molecular cell biology ·Vol. 5 ·No. 2 ·2004-02-00 ·Pages 148-57

Sedgwick B

Abstract

Methylating agents modify DNA at many different sites, thereby producing lethal and mutagenic lesions. To remove all the main harmful base lesions, at least three types of DNA-repair activities can be used, each of which involves a different reaction mechanism. These activities include DNA-glycosylases, DNA-methyltransferases and the recently characterized DNA-dioxygenases. The Escherichia coli AlkB dioxygenase and the two human homologues, ABH2 and ABH3, represent a novel mechanism of DNA repair. They use iron-oxo intermediates to oxidize stable methylated bases in DNA and directly revert them to the unmodified form.

MeSH Terms
AlkB Homolog 1, Histone H2a Dioxygenase Amino Acid Sequence Animals DNA Damage DNA Glycosylases/metabolism DNA Methylation DNA Modification Methylases/metabolism DNA Repair DNA Repair Enzymes Escherichia coli/genetics,metabolism Escherichia coli Proteins/chemistry,metabolism Humans Mixed Function Oxygenases/chemistry,metabolism Models, Molecular Molecular Sequence Data Molecular Structure Sequence Alignment
Chemicals
Escherichia coli Proteins Mixed Function Oxygenases AlkB protein, E coli ALKBH1 protein, human AlkB Homolog 1, Histone H2a Dioxygenase DNA Modification Methylases DNA Glycosylases DNA Repair Enzymes
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Sedgwick Barbara
Cancer Research UK London Research Institute, Clare Hall Laboratories, Blanche Lane, South Mimms, Hertfordshire EN6 3LD, UK. [email protected]
Article Info
Journal
Nature reviews. Molecular cell biology
Abbr.
Nat Rev Mol Cell Biol
ISSN
1471-0072
Published
2004-02-00
Pages
148-57
Language
English
Region
England
NLM ID
100962782
Subset
IM
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