Abstract
A DNase protection technique is described and applied to the interaction of three lac control proteins with supercoiled lac DNA. The technique uses end-labeled oligonucleotide primers to probe specific DNA regions as an alternative to protocols requiring restriction endonuclease cleavage or blotting. Thus DNA may be probed with high resolution in its native state. It is demonstrated that the introduction of supercoiling into DNA accelerates the rate of lac ps promoter binding by RNA polymerase but does not alter the positions at which polymerase, c-AMP-binding protein, or lac repressor bind to lac DNA.
MeSH Terms
Binding Sites
Chromosome Mapping
DNA, Superhelical/genetics
DNA-Directed RNA Polymerases/metabolism
Deoxyribonucleases
Escherichia coli/genetics
Kinetics
Lac Operon
Plasmids
Promoter Regions, Genetic
Receptors, Cyclic AMP/metabolism
Repressor Proteins/metabolism
Structure-Activity Relationship
Chemicals
DNA, Superhelical
Receptors, Cyclic AMP
Repressor Proteins
DNA-Directed RNA Polymerases
Deoxyribonucleases
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Gralla J D
References (16)
16 references, click to expand
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