Abstract:
:Base excision repair (BER) of damaged or inappropriate bases in DNA has been reported to take place by single nucleotide insertion or through incorporation of several nucleotides, termed short-patch and long-patch repair, respectively. We found that extracts from proliferating and non-proliferating cells both had capacity for single- and two-nucleotide insertion BER activity. However, patch size longer than two nucleotides was only detected in extracts from proliferating cells. Relative to extracts from proliferating cells, extracts from non-proliferating cells had approximately two-fold higher concentration of POLbeta, which contributed to most of two-nucleotide insertion BER. In contrast, two-nucleotide insertion in extracts from proliferating cells was not dependent on POLbeta. BER fidelity was two- to three-fold lower in extracts from the non-proliferating compared with extracts of proliferating cells. Furthermore, although one-nucleotide deletion was the predominant type of repair error in both extracts, the pattern of repair errors was somewhat different. These results establish two-nucleotide patch BER as a distinct POLbeta-dependent mechanism in non-proliferating cells and demonstrate that BER fidelity is lower in extracts from non-proliferating as compared with proliferating cells.
journal_name
DNA Repair (Amst)journal_title
DNA repairauthors
Akbari M,Peña-Diaz J,Andersen S,Liabakk NB,Otterlei M,Krokan HEdoi
10.1016/j.dnarep.2009.04.002subject
Has Abstractpub_date
2009-07-04 00:00:00pages
834-43issue
7eissn
1568-7864issn
1568-7856pii
S1568-7864(09)00096-2journal_volume
8pub_type
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