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Updated: Aug 14, 2026

Site-specific Bacterial Chromosome Engineering: ΦC31 Integrase Mediated Cassette Exchange (IMCE)
Published on: March 16, 2012
Molecular tools to detect the IncJ elements: a family of integrating, antibiotic resistant mobile genetic elements
Barry M McGrath1, John A O'Halloran, Anna V Piterina
1Molecular Biochemistry Laboratory, Department of Chemical and Environmental Sciences, University of Limerick, Limerick, Ireland.
Abstract:
The IncJ group of enterobacterial mobile genetic elements, which include R391, R392, R705, R997 and pMERPH, have been shown to be site-specific integrating elements encoding variable antibiotic and heavy metal resistance genes. They insert into a specific 17-bp site located in the prfC gene, encoding peptide release factor 3, in Escherichia coli and other hosts. A key feature of known IncJ elements is the presence of a site-specific recombination module consisting of an attachment site on the element and an integrase-encoding gene of the tyrosine recombinase class, which promotes integration between the attachment site on the element and a similar site on the host chromosome. We have cloned and sequenced the integrases from a number of known IncJ elements and designed PCR primers for specific amplification of this gene. Using conserved regions of enterobacterial prfC genes upstream and downstream of the insertion site, and conserved sequences at the ends of the integrated IncJ elements, we have designed specific primers to amplify across the integrated IncJ attL and attR junction fragments. Alignment of over 30 enterobacterial prfC-like genes indicates that the primers designed to amplify attR junction would amplify IncJ element: host junctions from a wide variety of hosts. The IncJ elements have been shown to sensitise recA(+)E. coli K12 strains to UV irradiation. A simple and rapid procedure for demonstrating this effect is described. These tools should enable the rapid detection of such elements in clinical and environmental settings.
Insights
Researchers developed new tools to detect IncJ mobile genetic elements, which carry antibiotic resistance genes. These elements integrate into the host genome at a specific site and can increase bacterial sensitivity to UV radiation, aiding in their identification in various settings.
Area of Science:
- Microbiology
- Genetics
- Molecular Biology
Background:
- IncJ elements are mobile genetic elements in enterobacteria, known for integrating into specific chromosomal sites and carrying resistance genes.
- These elements utilize a site-specific recombination system involving an integrase and attachment sites for integration into host genomes, specifically within the prfC gene.
Purpose of the Study:
- To develop novel molecular tools for the specific detection and characterization of IncJ mobile genetic elements.
- To investigate the functional consequences of IncJ element integration, such as increased sensitivity to UV irradiation.
Main Methods:
- Cloning and sequencing of integrase genes from known IncJ elements.
- Design and application of PCR primers targeting conserved regions of IncJ elements and host prfC genes for junction fragment amplification.
- Assessment of UV sensitivity in recA(+) E. coli strains harboring IncJ elements.
Main Results:
- Successful cloning and sequencing of IncJ integrases, enabling the design of specific PCR primers.
- Development of primers capable of amplifying IncJ element:host junctions across diverse bacterial hosts.
- Demonstration that IncJ elements sensitize E. coli to UV irradiation, providing a method for their detection.
Conclusions:
- The developed PCR-based tools facilitate the rapid and specific detection of IncJ mobile genetic elements in clinical and environmental samples.
- The observed UV sensitization effect offers an additional, functional assay for identifying the presence of these elements.
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