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Role of DNA polymerase I in excision-repair

Conference ·
OSTI ID:4126147

The ability of three different DNA polymerase I mutants of Escherichia coli to carry out excision-repair was examined. Strains having the same genetic origin but carrying either the polA1, polA107, resA1, or pol$sup +$ alleles were compared. The rate of ultraviolet-induced dimer excision was slightly reduced, relative to that found in Pol$sup +$ strains, in the PolA1 strain; greatly reduced in the PolA107 strain; and found not to occur in the ResA1 strain. Ultraviolet-light-induced repair synthesis as determined by the ultraviolet- stimulated incorporation of $sup 3$H-labeled 5-bromo-2'-deoxyuridine into DNA of the parental density showed that the polA1 mutation resulted in an increase in repair replication, while the presence of the polA107 allele caused a reduction in the amount of repair synthesis relative to that of the Pol$sup +$ strain. The ResA1 strain, however, showed no ultraviolet stimulation of the incorporation of the density label. These observations indicate that DNA polymerase I plays a key role in the excision-repair process in E. coli. (auth)

Research Organization:
Leiden State Univ.
NSA Number:
NSA-33-012270
OSTI ID:
4126147
Country of Publication:
United States
Language:
English