Abstract
E. coli mutants deficient in DNA polymerase I, in DNA polymerases I and II, or in DNA polymerase III, can efficiently and completely execute excision repair and post-replication repair of UV-damaged DNA at 43 degrees when assayed by alkaline sucrose gradients. Repair by cells deficient in polymerase I and in polymerases I and II is inhibited by 1-beta-D-arabinofuranosylcytosine at 43 degrees , whereas that by cells deficient in polymerase III is insensitive to the inhibitor. When both DNA polymerases I and III are deficient, both excision repair and post-replication repair are greatly reduced at 43 degrees , and the residual repair capability is inhibited by 1-beta-D-arabinofuranosylcytosine. Very little dark repair is observed in cells deficient in DNA polymerases I, II, and III, and the DNA is extensively degraded. These results suggest that either DNA polymerase I or DNA polymerase III is required for complete and efficient repair, and that when both DNA polymerases I and III are deficient, DNA polymerase II mediates a limited, incomplete dark repair of UV-damaged DNA. DNA polymerases I and III thus appear to be important enzymes in both DNA replication and DNA dark repair.
MeSH Terms
Carbon Radioisotopes
Centrifugation, Density Gradient
Cytarabine/pharmacology
DNA Nucleotidyltransferases/biosynthesis,metabolism
DNA Repair/drug effects
DNA, Bacterial/analysis,radiation effects
Depression, Chemical
Escherichia coli/enzymology,metabolism
Mutation
Radiation Effects
Temperature
Thymidine/metabolism
Thymine/metabolism
Ultraviolet Rays
Chemicals
Carbon Radioisotopes
DNA, Bacterial
Cytarabine
DNA Nucleotidyltransferases
Thymine
Thymidine
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Tait R C
Harris A L
Smith D W
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31 references, click to expand
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