A novel uracil-DNA glycosylase family related to the helix-hairpin-helix DNA glycosylase superfamily
Author(s) -
Ji Hyung Chung,
Eun Kyoung Im,
HyunYoung Park,
Jun Hye Kwon,
Seahyoung Lee,
Jaewon Oh,
Ki Chul Hwang,
Jong Ho Lee,
Yangsoo Jang
Publication year - 2003
Publication title -
nucleic acids research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 9.008
H-Index - 537
eISSN - 1362-4954
pISSN - 0305-1048
DOI - 10.1093/nar/gkg319
Subject(s) - dna glycosylase , uracil dna glycosylase , uracil , biology , dna , aquifex aeolicus , biochemistry , dna repair , cytosine , dna clamp , base excision repair , gene , rna , reverse transcriptase , escherichia coli
Cytosine bases can be deaminated spontaneously to uracil, causing DNA damage. Uracil-DNA glycosylase (UDG), a ubiquitous uracil-excising enzyme found in bacteria and eukaryotes, is one of the enzymes that repair this kind of DNA damage. To date, no UDG-coding gene has been identified in Methanococcus jannaschii, although its entire genome was deciphered. Here, we have identified and characterized a novel UDG from M.jannaschii designated as MjUDG. It efficiently removed uracil from both single- and double-stranded DNA. MjUDG also catalyzes the excision of 8-oxoguanine from DNA. MjUDG has a helix-hairpin-helix motif and a [4Fe-4S]-binding cluster that is considered to be important for the DNA binding and catalytic activity. Although MjUDG shares these features with other structural families such as endonuclease III and mismatch-specific DNA glycosylase (MIG), unique conserved amino acids and substrate specificity distinguish MjUDG from other families. Also, a homologous member of MjUDG was identified in Aquifex aeolicus. We report that MjUDG belongs to a novel UDG family that has not been described to date.
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