We have found that the bacterial transposon Tn7 can recognize and preferent
ially insert adjacent to triple-helical nucleic acid structures. Both synth
etic intermolecular triplexes, formed through the pairing of a short triple
r-forming oligonucleotide on a plasmid DNA, and naturally occurring mirror
repeat sequences known to form intramolecular triplexes or H-form DNA are p
referential targets for Tn7 insertion in vitro. This target site selectivit
y depends upon the recognition of the tripler region by a Tn7-encoded ATP-u
sing protein, TnsC, which controls Tn7 target site selection: the interacti
on of TnsC with the tripler region results in recruitment and activation of
the Tn7 transposase, Recognition of a nucleic acid structural motif provid
es both new information into the factors that influence Tn7's target site s
election and broadens its targeting capabilities.