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PMID: 9302014 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Two abundant intramolecular transposition products, resulting from reactions initiated at a single end, suggest that IS2 transposes by an unconventional pathway.

Molecular microbiology ·Vol. 25 ·No. 3 ·1997-08-00 ·Pages 517-29

Lewis LA, Grindley ND

Abstract

The Escherichia coli insertion sequence, IS2, is a member of the IS3 family of bacterial transposable elements. Its transposase is a fusion protein, OrfAB, made by a programmed -1 translational frameshift near to the end of orfA and just after the start of orfB. We have characterized two major products of IS2 intramolecular transposition, which accumulate in cells that express the IS2 OrfAB fusion protein at elevated levels. The more abundant product is a minicircle composed of the complete IS2 with just a single basepair (occasionally 2bp) separating the two IS ends. In all cases, this basepair is derived from the vector sequence immediately adjacent to the left IS2 end (IRL). The second product is a figure-eight molecule that contains all the IS2 and vector sequences present in the parental plasmid. One DNA strand contains the parental sequences unrearranged. The other contains a single-stranded version of the minicircle junction--the precise 3' end of IRR has been cleaved and joined to a target just outside the 5' end of IRL; the remaining vector sequences have a free 5' end, derived from cleavage at the 3' end of IRR, and a free 3' end, released upon cleavage of the target site adjacent to IRL. We propose that figure-eight molecules are the precursor to IS2 minicircles and that the formation of these two products is the initial step in IS2 intermolecular transposition. This proposed transposition pathway provides a means for a transposase that can cleave only one strand at each IS end to produce simple insertions and avoid forming co-integrates.

MeSH Terms
Bacterial Proteins/genetics,metabolism Base Sequence Binding Sites/genetics Cloning, Molecular DNA Nucleotidyltransferases/genetics,metabolism DNA Primers/genetics DNA Transposable Elements/genetics DNA, Bacterial/chemistry,genetics,metabolism DNA, Circular/genetics,metabolism Escherichia coli/genetics,metabolism Escherichia coli Proteins Microscopy, Electron Models, Genetic Molecular Sequence Data Nucleic Acid Conformation Polymerase Chain Reaction Recombinant Fusion Proteins/genetics,metabolism Transposases
Chemicals
Bacterial Proteins DNA Primers DNA Transposable Elements DNA, Bacterial DNA, Circular Escherichia coli Proteins OrfB protein, E coli Recombinant Fusion Proteins DNA Nucleotidyltransferases Transposases
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Lewis L A
Department of Molecular Biophysics and Biochemistry, Yale University, New Haven, CT 06520-8114, USA. [email protected]
Grindley N D
Article Info
Journal
Molecular microbiology
Abbr.
Mol Microbiol
ISSN
0950-382X
Published
1997-08-00
Pages
517-29
Language
English
Region
England
NLM ID
8712028
Subset
IM
Grants
NIGMS NIH HHS · GM08153 · United States
NIGMS NIH HHS · GM16060 · United States
NIGMS NIH HHS · GM28470 · United States
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