Recombination between two TnA transposon sequences oriented as inverse repeats is found less frequently than between direct repeats

Abstract
Inverse repeats of the transposon Tn2660 in either a ColEl or an R6K replicon, with or without inversions of the parental DNA sequences between the repeats, show no detectable (recA or recA + hosts. In contrast, attempts made to construct plasmids which carry two direct repeats by in vitro cleavage and ligation in a recA host were unsuccessful, although homologous plasmids with inverse repeats could be constructed, and other plasmids were found consistent with products of recombination between the direct repeats of a transient intermediate structure. It is concluded that in recA or recA + hosts recombination between direct repeats of a transposon is frequent, whereas recombination between inverse repeats of a homologous structure has not been observed. A model to explain this difference depends upon a mechanism that produces a nick in only one of the pair of strands at the internal resolution site (IRS) sequence of the transposon.