The reaction of guanine residues with dimethylsulfate was studied for
complexes of recA protein with fluorescent dye tagged double stranded
oligonucleotides. The patterns of dimethylsulfate modification obtaine
d demonstrate a similarity of DNA states in the complexes with recA pr
otein formed as a result of recA promoted strand exchange and renatura
tion reactions. The guanine modification efficiency varies periodicall
y as a function of the base position along the oligonucleotide axis, w
ith a period of 3 nucleotides. This effect suggests that the arrangeme
nt of recA monomers along the oligonucleotide is strictly ordered, and
the dimethylsulfate reactivity of a guanine residue depends on the si
te of its binding in a recA monomer. (C) 1997 Federation of European B
iochemical Societies.