Base excision repair of DNA in mammalian cells

Citation
He. Krokan et al., Base excision repair of DNA in mammalian cells, FEBS LETTER, 476(1-2), 2000, pp. 73-77
Citations number
36
Categorie Soggetti
Biochemistry & Biophysics
Journal title
FEBS LETTERS
ISSN journal
00145793 → ACNP
Volume
476
Issue
1-2
Year of publication
2000
Pages
73 - 77
Database
ISI
SICI code
0014-5793(20000630)476:1-2<73:BERODI>2.0.ZU;2-I
Abstract
Base excision repair (BFR) of DNA corrects a number of spontaneous and envi ronmentally induced genotoxic or miscoding base lesions in a process initia ted by DNA glycosylases. An AP endonuclease cleaves at the 5' side of the a basic site and the repair process is subsequently completed via either shor t patch repair or long patch repair, which largely require different protei ns. As one example, the UNG gene encodes both nuclear (UNG2) and mitochondr ial (UNG1) uracil DNA glycosylase and prevents accumulation of uracil in th e genome. BER is likely to have a major role in preserving the integrity of DNA during evolution and may prevent cancer. (C) 2000 Federation of Europe an Biochemical Societies. Published by Elsevier Science B,V. All rights res erved.