Like many transposons the bacterial insertion sequence IS903 was thought to
insert randomly. However, using both genetic and statistical approaches, w
e have derived a target site for IS903 that is used 84% of the time. Comput
ational and genetic analyses of multiple IS903 insertion sites predicted a
preferred target consisting of a 21 bp palindromic pattern centered on the
9 bp target duplication generated during transposition. Here we show that t
argeting can be dissected into four components: the 5 bp flanking sequences
, the most important sequences required for site-specific insertion; the 7
bp palindromic core within the target duplication; the dinucleotide pair at
the transposon-target junction; and the local DNA context. Finally, using
a substrate with multiple target sites we show that a target site is more l
ikely found by a local bind-and-slide model and not by extended DNA trackin
g. (C) 2001 Academic Press.