TY - JOUR
T1 - Transposases are responsible for the target specificity of IS1397 and ISKpn1 for two different types of palindromic units (PUs)
AU - Wilde, Caroline
AU - Escartin, Frédéric
AU - Kokeguchi, Susumu
AU - Latour-Lambert, Patricia
AU - Lectard, Aude
AU - Clément, Jean Marie
N1 - Funding Information:
We thank M. Chandler for helpful advice about the manuscript. This work was supported in part by the `Programme de Recherche Fondamentale en Microbiologie et Maladies Infectieuses et Parasitaires' from `MinisteÁre FrancËais de l'Education Nationale de la Recherche et de la Technologie'. C.W. was supported by a grant from the `Fondation pour la Recherche Médicale'.
PY - 2003/8/1
Y1 - 2003/8/1
N2 - Insertion sequences (IS)1397 and ISKpn1, found in Escherichia coli and Klebsiella pneumoniae respectively, are IS3 family members that insert specifically into short palindromic repeated sequences (palindromic units or PUs). In this paper, we first show that although PUs are naturally absent from extrachromosomal elements, both ISs are able to transpose from the chromosome or from a plasmid into PUs artificially introduced into target plasmids. We also show that ISKpn1 target specificity is restricted to K.pneumoniae Z1 PU type, whereas IS1397 target specificity is less stringent since the IS fargets the three E.coli Y, Z1 and Z2 PU types indifferently. Experiments of transposition of both ISs driven by both transposases demonstrate that the inverted repeats flanking the ISs are not responsible for this target specificity, which is entirely due to the transposase itself. Implications on ISs evolution are presented.
AB - Insertion sequences (IS)1397 and ISKpn1, found in Escherichia coli and Klebsiella pneumoniae respectively, are IS3 family members that insert specifically into short palindromic repeated sequences (palindromic units or PUs). In this paper, we first show that although PUs are naturally absent from extrachromosomal elements, both ISs are able to transpose from the chromosome or from a plasmid into PUs artificially introduced into target plasmids. We also show that ISKpn1 target specificity is restricted to K.pneumoniae Z1 PU type, whereas IS1397 target specificity is less stringent since the IS fargets the three E.coli Y, Z1 and Z2 PU types indifferently. Experiments of transposition of both ISs driven by both transposases demonstrate that the inverted repeats flanking the ISs are not responsible for this target specificity, which is entirely due to the transposase itself. Implications on ISs evolution are presented.
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U2 - 10.1093/nar/gkg494
DO - 10.1093/nar/gkg494
M3 - Article
C2 - 12888493
AN - SCOPUS:0041660964
SN - 0305-1048
VL - 31
SP - 4345
EP - 4353
JO - Nucleic acids research
JF - Nucleic acids research
IS - 15
ER -