Structural and functional analysis of Tn4430: identification of an integrase-like protein involved in the co-integrate-resolution process

EMBO J. 1988 May;7(5):1515-26. doi: 10.1002/j.1460-2075.1988.tb02971.x.

Abstract

The 4149-bp transposon Tn4430 from Bacillus thuringiensis is delineated by 38-bp inverted repeats and codes for a 113-kd protein that shares homology with the transposases (TnpA) of Tn3, Tn21 and Tn501. Through transpositional recombination, this protein generates the formation of co-integrates between both donor and target replicons, with duplication of Tn4430 molecules. These features are characteristic of transposons of the Tn3 family (class II elements). The second step of the transposition process, the co-integrate resolution, is mediated by a 32-kd protein. This protein (TnpI) displays regional similarities with site-specific recombinases of the integrase family, such as Int of bacteriophage lambda, Cre of bacteriophage P1 or TnpA and TnpB of the Tn554 transposon. Moreover, the 250-bp sequence upstream to the tnpI gene contains several structural features that are reminiscent of the attP attachment site of phage lambda. This unique association between the integrase-like TnpI recombinase and the TnpA transposase qualifies Tn4430 as a member of a new group within the class II mobile genetic elements.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Bacillus thuringiensis / enzymology
  • Bacillus thuringiensis / genetics*
  • Base Sequence
  • DNA Nucleotidyltransferases / genetics*
  • DNA Nucleotidyltransferases / metabolism
  • DNA Transposable Elements*
  • DNA, Bacterial / genetics
  • Escherichia coli / enzymology
  • Escherichia coli / genetics
  • Integrases
  • Molecular Sequence Data
  • Nucleotidyltransferases / genetics
  • Nucleotidyltransferases / metabolism
  • Recombination, Genetic
  • Transposases

Substances

  • DNA Transposable Elements
  • DNA, Bacterial
  • DNA Nucleotidyltransferases
  • Integrases
  • Nucleotidyltransferases
  • Transposases