Why Do Unrelated Insertion Sequences Occur Together in the Genome of Escherichia coli?

• Published in: Genetics (Austin) 1988-03, Vol.118 (3), p.537-541
• Main Authors: Hartl, D. L, Sawyer, S. A
• Format: Article
• Language: English
• Subjects: Biological and medical sciences; DNA Transposable Elements; Escherichia coli; Escherichia coli - genetics; Fundamental and applied biological sciences. Psychology; Genes, Bacterial; Genic rearrangement. Recombination. Transposable element; Investigations; Mathematics; Models, Genetic; Molecular and cellular biology; Molecular genetics; Polymorphism, Genetic
• ISSN: 0016-6731; 1943-2631; 1943-2631
• DOI: 10.1093/genetics/118.3.537

Natural isolates of Escherichia coli are polymorphic for the presence or absence of insertion sequences. Among the ECOR reference collection of 71 natural isolates studied for the number of copies of the insertion sequences IS1, IS2, IS3, IS4, IS5 and IS30, the number of strains containing no copies of the insertion sequences were 11, 28, 23, 43, 46 and 36, respectively. Significant correlations occur in the ECOR strains in the presence or absence of unrelated insertion sequences in the chromosome and plasmid complements. Strains containing any insertion sequence are more likely to contain additional, unrelated insertion sequences than would be expected by chance. We suggest that the positive correlations result from horizontal transfer mediated by plasmids. A branching-process model for the plasmid-mediated transmission of insertion sequences among hosts yields such a correlation, even in the absence of interactions affecting transposition or fitness. The predictions of the model are quantitatively in agreement with the observed correlations among insertion sequences.