potassium-permanganate and chloroacetaldehyde

Bacteriophage N4 virion RNA polymerase promoters contain five to seven-base inverted repeats separated by three bases and centered at position -12 from the site of transcription initiation. We have previously shown that these inverted repeats extrude as hairpins at physiological superhelical densities in a Mg(II)-dependent manner. Mg(II)-dependent hairpin extrusion at promoters P1 and P2 displays quantitative differences in reactivity to structural probes at different DNA superhelical densities, with extrusion at P2 being more favored at low superhelical density. Analyses of mutant promoters using structure-specific probes revealed that specific sequences, at the closing base-pair of the hairpin and at the loop (i.e. 5'-C-GXA-G-3' where X=G, A, T), are required for extrusion of the small promoter hairpins at physiological superhelical density. The sequence-dependent requirements for extrusion of the small N4 promoter hairpins may be generally applicable for other such sequences found both in prokaryotic and eukaryotic genomes.

Topics: Acetaldehyde; Base Sequence; Conserved Sequence; DNA-Directed RNA Polymerases; DNA, Superhelical; DNA, Viral; Mutation; Nucleic Acid Conformation; Podoviridae; Potassium Permanganate; Promoter Regions, Genetic; Repetitive Sequences, Nucleic Acid; Single-Strand Specific DNA and RNA Endonucleases; Virion