Affiliation:
1. Sydney Laboratory, CSIRO Molecular Science, North Ryde 2113,1 and
2. Department of Biological Sciences, Macquarie University Sydney, Sydney 2109,2 Australia
Abstract
ABSTRACT
The first 13.6 kb of the mercury and multidrug resistance transposon Tn
1696
, which includes the class 1 integron In4, has been sequenced. In4 is 8.33 kb long and contains the 5′-conserved segment (5′-CS) and 2.24 kb of the 3′-conserved segment (3′-CS) flanking four integrated cassettes. The 3′-CS region is followed by one full copy and an adjacent partial copy of the insertion sequence IS
6100
flanked, in inverse orientation, by two short segments (123 and 152 bp) from the outer right-hand end of class 1 integrons. This structure is representative of a distinct group of class 1 integrons that differs from In2, found in Tn
21
, and other related class 1 integrons. In4 does not include transposition genes but is bounded by characteristic 25-bp inverted repeats and flanked by a direct duplication of 5 bp of the target sequence, indicating that it was inserted by a transpositional mechanism. In4 lies between the
resII
and
resI
sites of a backbone mercury resistance transposon which is >99.5% identical to Tn
5036
. Although Tn
21
and Tn
1696
are both classified as members of the Tn
21
subfamily of the Tn
3
transposon family, the backbone mercury resistance transposons are only 79 to 96% identical. Tn
21
also contains a region of about 0.7 kb not found in Tn
1696
. The integrons In2 and In4 carrying the antibiotic resistance genes have been inserted at different locations into distinct ancestral mercury resistance transposons. Thus, Tn
21
and Tn
1696
have independent histories and origins. Other transposons (Tn
1403
and Tn
1412
) that include a class 1 integron also have independent origins. In all except Tn
21
, the integron is located within the
res
region of the backbone transposon.
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Pharmacology (medical),Pharmacology
Cited by
211 articles.
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