Abstract
The effect on DNA repair of several inhibitors of DNA synthesis has been investigated in CHO cells. Three assays were employed following ultraviolet irradiation of G1 cells: unscheduled DNA synthesis, removal of antibody binding sites and alkaline elution. Cytosine arabinoside and aphidicolin were found to reduce unscheduled DNA synthesis in a dose-dependent manner without affecting the removal of antibody-binding sites. Strand rejoining was also inhibited. These results are consistent with the hypothesis that inhibition is due to premature chain termination during repair synthesis some time after excision of the lesion. Conversely, inhibition of unscheduled DNA synthesis by novobiocin is paralleled by inhibition of excision of the lesion. However, no inhibition of incision was apparent. Since nalidixic acid, an inhibitor of topoisomerase II, did not inhibit excision, it is unlikely that the primary site of action of novobiocin is this topoisomerase. The possibility that a second topoisomerase and/or a polymerase are affected is discussed in the light of previously published data.
Original language | English (US) |
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Pages (from-to) | 355-361 |
Number of pages | 7 |
Journal | BBA - Gene Structure and Expression |
Volume | 740 |
Issue number | 4 |
DOIs | |
State | Published - Sep 9 1983 |
Keywords
- (Chinese hamster ovary cell)
- Aphidicolin
- Cytosine arabinoside
- DNA repair
- DNA synthesis inhibitor
- Nalidixic acid
- Novobiocin
ASJC Scopus subject areas
- Structural Biology
- Biophysics
- Biochemistry
- Genetics