This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Olasz, F.
Right arrow Articles by Arber, W.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Olasz, F.
Right arrow Articles by Arber, W.

 Previous Article  |  Next Article 

J. Bacteriol., Dec 1997, 7551-7558, Vol 179, No. 23
Copyright © 1997, American Society for Microbiology

Terminal inverted repeats of insertion sequence IS30 serve as targets for transposition

F Olasz, T Farkas, J Kiss, A Arini and W Arber
Department of Microbiology, Biozentrum, University of Basel, Switzerland. olasz@hubi.abc.hu

In the present study, we demonstrate that the terminal inverted repeats of the Escherichia coli insertion sequence IS30 are functional target sites for the transposition of the (IS30)2 dimer, which represents an intermediate structure in the transposition of IS30. Comparative analysis of various target regions revealed that the left and right ends differ in their "attractivity." In our experiments, the joined left and right ends, i.e., the (IS30)2 intermediate structure, was found to be the most preferred target. It was also shown that flanking sequences can influence the target activity of the terminal repeats. The functional part of the target region was localized in the inverted repeats by means of mutational analysis, and it corresponds to the binding site of IS30 transposase. Insertion of 1 bp into the right inverted repeat resulted in unusual target duplication accompanied by gene conversion. The choice of the terminal inverted repeats as targets in transposition leads to the reconstruction of the (IS30)2 structure, which may induce a cascade of further rearrangements. Therefore, this process can play a role in the evolution of the genome.


This article has been cited by other articles:

  • Bai, X., Zhang, J., Ewing, A., Miller, S. A., Jancso Radek, A., Shevchenko, D. V., Tsukerman, K., Walunas, T., Lapidus, A., Campbell, J. W., Hogenhout, S. A. (2006). Living with genome instability: the adaptation of phytoplasmas to diverse environments of their insect and plant hosts.. J. Bacteriol. 188: 3682-3696 [Abstract] [Full Text]  
  • Kiss, J., Szabo, M., Olasz, F. (2003). Site-specific recombination by the DDE family member mobile element IS30 transposase. Proc. Natl. Acad. Sci. USA 100: 15000-15005 [Abstract] [Full Text]  
  • Szeverenyi, I., Nagy, Z., Farkas, T., Olasz, F., Kiss, J. (2003). Detection and analysis of transpositionally active head-to-tail dimers in three additional Escherichia coli IS elements. Microbiology 149: 1297-1310 [Abstract] [Full Text]  
  • Hall, B. G. (1999). Spectra of Spontaneous Growth-Dependent and Adaptive Mutations at ebgR. J. Bacteriol. 181: 1149-1155 [Abstract] [Full Text]  
  • Rudant, E., Courvalin, P., Lambert, T. (1998). Characterization of IS18, an Element Capable of Activating the Silent aac(6')-Ij Gene of Acinetobacter sp. 13 Strain BM2716 by Transposition. Antimicrob. Agents Chemother. 42: 2759-2761 [Abstract] [Full Text]