Abstract
The ultraviolet (UV)-induced (6-4) pyrimidine-pyrimidone photoproduct [(6-4) PP] confers a large structural distortion in DNA. Here we examine in human cells the roles of translesion synthesis (TLS) DNA polymerases (Pols) in promoting replication through a (6-4) TT photoproduct carried on a duplex plasmid where bidirectional replication initiates from an origin of replication. We show that TLS contributes to a large fraction of lesion bypass and that it ismostly error-free. We find that, whereas Pol h and Pol i provide alternate pathways for mutagenic TLS, surprisingly, Pol ζ functions independently of these Pols and in a predominantly error-free manner. We verify and extend these observations in mouse cells and conclude that, in human cells, TLS during replication can be markedly error-free even opposite a highly distorting DNA lesion.
Original language | English (US) |
---|---|
Pages (from-to) | 123-128 |
Number of pages | 6 |
Journal | Genes and Development |
Volume | 24 |
Issue number | 2 |
DOIs | |
State | Published - Jan 15 2010 |
Keywords
- (6-4) photoproducts
- DNA repair
- DNA replication
- Replicative lesion bypass
- UV damage
ASJC Scopus subject areas
- General Medicine