Abstract
Short DNA duplexes are protected when lambda DNA is digested with nuclease in the presence of lambda repressor. As the ratio of repressor to operator is increased, six successively larger fragments are recovered, ranging in size from 35 to 100 base pairs, each of which binds repressor. Study of these fragments indicates that, at each of the two lambda operators (o(L) and o(R)), repressor first binds to a unique site (not necessarily terminal), and that five additional sites are then filled in linear right-ward or left-ward order. The nucleotide sequences and affinities for repressor of o(L) and o(R) are not identical, although six fragments of similar size are protected at each operator. Evidence is presented arguing against the existence of hairpin-like structures in the operator fragments, and, moreover, it is shown that the operator duplex does not unwind when repressor binds to it.
MeSH Terms
Autoradiography
Binding Sites
Chromatography, DEAE-Cellulose
Chromatography, Gel
Coliphages
DNA, Circular/analysis
DNA, Single-Stranded/analysis
DNA, Viral/analysis,isolation & purification
Deoxyribonucleases/metabolism
Electrophoresis, Polyacrylamide Gel
Genes, Regulator
Molecular Weight
Mutation
Nucleic Acid Denaturation
Phosphorus Isotopes
Pyrimidines/analysis
Chemicals
DNA, Circular
DNA, Single-Stranded
DNA, Viral
Phosphorus Isotopes
Pyrimidines
Deoxyribonucleases
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Maniatis T
Ptashne M
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