NEIL1 excises 3' end proximal oxidative DNA lesions resistant to cleavage by NTH1 and OGG1

Nucleic Acids Res. 2005 Aug 29;33(15):4849-56. doi: 10.1093/nar/gki816. Print 2005.

Abstract

Base excision repair is the major pathway for the repair of oxidative DNA damage in human cells that is initiated by a damage-specific DNA glycosylase. In human cells, the major DNA glycosylases for the excision of oxidative base damage are OGG1 and NTH1 that excise 8-oxoguanine and oxidative pyrimidines, respectively. We find that both enzymes have limited activity on DNA lesions located in the vicinity of the 3' end of a DNA single-strand break, suggesting that other enzymes are involved in the processing of such lesions. In this study, we identify and characterize NEIL1 as a major DNA glycosylase that excises oxidative base damage located in close proximity to the 3' end of a DNA single-strand break.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Base Sequence
  • DNA Damage*
  • DNA Glycosylases / metabolism*
  • DNA Repair*
  • Deoxyribonuclease (Pyrimidine Dimer) / metabolism
  • Guanine / analogs & derivatives
  • Guanine / metabolism
  • Humans
  • Oligonucleotides / chemistry
  • Oligonucleotides / metabolism
  • Oxidative Stress*
  • Substrate Specificity
  • Uracil / analogs & derivatives
  • Uracil / metabolism

Substances

  • Oligonucleotides
  • 5-hydroxyuracil
  • 8-hydroxyguanine
  • Uracil
  • Guanine
  • Deoxyribonuclease (Pyrimidine Dimer)
  • NTHL1 protein, human
  • DNA Glycosylases
  • NEIL1 protein, human
  • oxoguanine glycosylase 1, human