NEIL1 is the major DNA glycosylase that processes 5-hydroxyuracil in the proximity of a DNA single-strand break

Jason L Parsons, Bodil Kavli, Geir Slupphaug, Grigory L Dianov

Research output: Contribution to journalArticlepeer-review

Abstract

5-Hydroxyuracil (5-OHU) in DNA, arising during endogenous DNA damage and caused by ionizing radiation, is removed by the base excision repair pathway. However, in addition to base lesions, ionizing radiation also generates DNA single-strand breaks (SSBs). When these DNA lesions are located in the proximity of each other, this may result in a profound effect on both repair of the damaged base and the SSB. We therefore examined the repair of DNA substrates containing 5-OHU lesions in the proximity of the 3'-end of a SSB. We found that SSB repair by DNA ligase IIIalpha and DNA polymerase beta is impaired by the presence of the nearby 5-OHU lesion, indicating the requirement for a DNA glycosylase which would be able to remove 5-OHU before SSB repair. Subsequently, we found that although both SMUG1 and NEIL1 are able to excise 5-OHU lesions located in the proximity of the 3'-end of a DNA SSB, NEIL1 is more efficient in the repair of these DNA lesions.

Original languageEnglish
Pages (from-to)4158-63
Number of pages6
JournalBiochemistry
Volume46
Issue number13
DOIs
Publication statusPublished - 3 Apr 2007

Keywords

  • DNA Damage
  • DNA Glycosylases/metabolism
  • DNA Ligase ATP
  • DNA Ligases/metabolism
  • DNA Polymerase beta/metabolism
  • DNA Repair/physiology
  • Humans
  • Poly-ADP-Ribose Binding Proteins
  • Uracil/analogs & derivatives
  • Uracil-DNA Glycosidase/metabolism
  • Xenopus Proteins

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