Аңдатпа
Aerobic cellular respiration generates reactive oxygen species (ROS), which can damage macromolecules including lipids, proteins and DNA.It was proposed that aging is a consequence of accumulation naturally occurring unrepaired oxidative DNA damage.In human cells, on average approximately 2000 to 8000 DNA lesions occur per hour in each cell, or about 40000 to 200000 per cell per day.DNA repair systems are able to discriminate between regular and modified bases.For example, DNA glycosylases specifically recognize and excise damaged bases among vast majority of regular bases in the base excision repair (BER) pathway.However, mismatched pairs between two regular bases occur due to spontaneous conversion of 5-methylcytosine to thymine and DNA polymerase errors during replication.To counteract these mutagenic threats to genome stability, cells evolved special DNA repair systems that target the non-damaged DNA strand in a duplex to remove mismatched regular DNA bases.Mismatch-specific adenine-and thymine-DNA glycosylases (MutY/MUTYH and TDG/MBD4, respectively) initiated base excision repair (BER) and mismatch repair (MMR) pathways can recognize and remove normal DNA bases in mismatched DNA duplexes.Paradoxically, under certain circumstances in DNA repair deficient cells bacterial MutY and human TDG can act in the aberrant manner: MutY and TDG removes Adenine and Thymine opposite misincorporated 8-oxoguanine and damaged Adenine, respectively.These unusual activities lead either to mutations or futile DNA repair, thus indicating that the DNA repair pathways which target non-damaged DNA strand can act in aberrant manner and introduce genome instability in the presence of unrepaired DNA lesions.Evidences gathered showing that in addition to the accumulation of oxidative DNA damage in cells, the aberrant DNA repair can also contribute to cancer, brain disorders and premature senescence.This review summarises the present knowledge about the aberrant DNA repair pathways for oxidised base modifications and their possible role in aging. K e y w o r d s: oxidative DNA damage; crystal structure; base excision repair; nucleotide incision repair; AP endonuclease.