Affiliation:
1. Sydney Laboratory, CSIRO Molecular Science, North Ryde, New South Wales 1670
2. Department of Biological Sciences, Macquarie University, Sydney, New South Wales 2109, Australia
Abstract
ABSTRACT
Integrons capture gene cassettes by using a site-specific recombination mechanism. As only one class of integron and integron-determined site-specific recombination system has been studied in detail, the properties of a second class, the only known class 3 integron, were examined. The configuration of the three potentially definitive features of integrons, the
intI3
gene, the adjacent
attI3
recombination site, and the P
c
promoter that directs transcription of the cassettes, was similar to that found in the corresponding region (5′ conserved segment) of class 1 integrons. The integron features are flanked by a copy of the terminal inverted repeat, IRi, from class 1 integrons on one side and a resolvase-encoding
tniR
gene on the other, suggesting that they are part of a transposable element related to Tn
402
but with the integron module in the opposite orientation. The IntI3 integrase was active and able to recognize and recombine both known types of IntI-specific recombination sites, the
attI3
site in the integron, and different cassette-associated 59-be (59-base element) sites. Both integration of circularized cassettes into the
attI3
site and excision of integrated cassettes were also catalyzed by IntI3. The
attI3
site was localized to a short region adjacent to the
intI3
gene. Recombination between a 59-be and secondary sites was also catalyzed by IntI3, but at frequencies significantly lower than observed with IntI1, the class 1 integron integrase.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
Cited by
104 articles.
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