Mutagenesis of the lac promoter region in M13 mp10 phage DNA by 4'-hydroxymethyl-4,5',8-trimethylpsoralen.

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Abstract
Double-stranded M13 phage DNA (M13 mp10 replicative form) was photoreacted with 4''-hydroxymethyl-4,5'',8-trimethylpsoralen, using light of wavelength > 320 nm or > 390 nm to generate predominantly crosslinks or monoadducts, respectively. The damaged DNAs were scored for inactivation and mutagenesis after transfection into Escherichia coli. The appearance of light-blue or colorless plaques on indicator medium showed that mutation had occurred in the lac insert of the viral DNA. A comparison of the consequences of the two phototreatments with psoralen supports the idea that crosslinks are both more lethal and more multagenic than monoadducts. Numerous mutant clones partially or totally deficient in .beta.-galactosidase were plaque-purified and amplified. The viral DNA of each clone was sequenced by the dideoxy chain-terminating procedure. All of the observed base-pair changes were mapped to the lac promoter region and consisted of 3 transition, 14 transversion, and 6 single base-pair frame-shift mutations. The predominant mutation was a T .cntdot. A .fwdarw. G .cntdot. C transversion.