Affiliation:
1. School of Life and Environmental Sciences, The University of Sydney, NSW 2006, Australia
Abstract
Several insertion sequences (IS) found in various
Acinetobacter
species exhibit target specificity. They are found, in the same orientation, 5 bp from the XerC binding site of the pdif sites associated with dif modules in
Acinetobacter
plasmids, and searches revealed they are also found near chromosomal dif sites of
Acinetobacter
species. These IS are 1.5 kb long, bounded by 24–26 bp imperfect terminal inverted repeats (TIRs) and encode a large transposase of 441–457 aa. They generate 5 bp target site duplications (TSDs). Structural predictions of the ISAjo2 transposase, TnpAjo2, modelled on TnsB of Tn7 revealed two N-terminal HTH domains followed by an RNaseH fold (DDE domain), a β barrel and a C-terminal domain. Similar to Tn7, the outer IS ends are 5′-TGT and ACA-3′, and an additional Tnp binding site, corresponding to the internal portion of the IR, is found near each end. However, the
Acinetobacter
IS do not encode further proteins related to those required by Tn7 for targeted transposition, and the transposase may interact directly with XerC bound to a dif-like site. We propose that these IS, currently in the IS1202 group in the not characterized yet (NCY) category in ISFinder, are part of a distinct IS1202 family. Other IS listed as in the IS1202 group encode transposases related to TnpAjo2 (25–56 % amino acid identity) and have similar TIRs but fall into three groups based on the TSD length (3–5, >15, 0 bp). Those with 3–5 bp TSDs may also target dif-like sites but targets were not found for the other groups.
Funder
National Health and Medical Research Council
Cited by
5 articles.
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