4.8 Article

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

Journal

NUCLEIC ACIDS RESEARCH
Volume 33, Issue 15, Pages 4849-4856

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/nar/gki816

Keywords

-

Funding

  1. Wellcome Trust Funding Source: Medline

Ask authors/readers for more resources

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.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.8
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available