PMID:8702929
| Citation |
Ahn, B and Grossman, L (1996) The binding of UvrAB proteins to bubble and loop regions in duplex DNA. J. Biol. Chem. 271:21462-70 |
|---|---|
| Abstract |
Based on the binding of the UvrAB complex to a promoter region in transcription open complexes (Ahn, B., and Grossman, L. (1996) J. Biol. Chem. 271, 21453-21461) and the requirement of a single-stranded region for UvrAB helicase activity, we examined the binding of UvrAB proteins to synthetic bubble or loop regions in duplex DNA and the role of these regions in translocation of the UvrAB complex as well as incision of DNA damage. We found that the UvrAB complex was able to bind to bubble and loop regions with an affinity similar to that for damaged DNA in the absence of RNAP. The preferential recognition and incision of damaged sites by the UvrAB complex was observed downstream of the bubble or loop region in the strand complementary to the strand along which the UvrAB complex translocates. These results imply that the bubble region generated in duplex DNA by RNAP serves as a preferred entry site for the translocation of the UvrAB complex, and that preferential binding and unidirectional translocation of the UvrAB complex predetermine where incision is to occur. |
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| Keywords |
Adenosine Triphosphatases/metabolism; Bacterial Proteins/metabolism; Base Sequence; Biological Transport; Blotting, Western; DNA Damage; DNA Helicases; DNA, Recombinant/metabolism; DNA, Recombinant/radiation effects; DNA-Binding Proteins/metabolism; DNA-Directed RNA Polymerases/metabolism; Escherichia coli Proteins; Kinetics; Molecular Sequence Data; Potassium Permanganate/chemistry; Protein Binding; Ultraviolet Rays |
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