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Does Tn10 transpose via the cointegrate molecule?

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Summary

It has been well established that Tn3 and its relatives transpose from one replicon to another by two successive reactions: formation of the cointegrate molecule and resolution from it. Whether or not the 9300 base pair tetracycline resistance transposon Tn10 transposes in the same manner as Tn3 was investigated by two methods.

In the first method, λ55, a lambda phage carrying Tn10 was lysogenized in an Escherichia coli strain carrying a Tn10 insertion; the phage has a deletion in attP, hence it was lysogenized in a Tn10 sequence in the E. coli chromosome by reciprocal recombination. The chromosomal structure in these lysogens is equivalent to the Tn10-mediated cointegrate molecule of lambda and the E. coli chromosomal DNA. The stability of the cointegrate molecule was examined by measuring the rate of excision of lambda from the host chromosome, and was found to be stable, especially in a Rec- strain. Because of this stability, the cointegrate molecule should be accumulated if Tn10 transposes via the cointegrate molecule. Then, we examined the configuration of products made by transposition of Tn10 from λ55 to the E. coli chromosome. The cointegrate molecule was found in products of Tn10 transposition in a Rec+ strain at a frequency of 5% per Tn10 transposition, but this molecule could not be found in a Rec- strain. Since transposition of Tn10 was recA-independent, absence of the cointegrate molecule formed in a RecA- strain strongly suggested that the cointegrate molecule is not an obligatory intermediate of transposition of Tn10.

In the second method, mobilization of pACYC177 by R388 and by R388:: Tn10 was examined. The pACYC177 plasmid was mobilized by R388::Tn10 at a frequency of 10-4 per donor but not by R388. It occurred, in most cases, by “inverse transposition” of R388::Tn10 to pACYC177 forming plasmids such as pACYC177::IS10-R388-IS10. Mobilization of pACYC177 by a Tn10-mediated cointegrate in the form of pACYC177::Tn10-R388-Tn10 was not observed in crosses using a Rec- donor. These observations also suggested that transposition of Tn10 in Rec- cells does not occur via the cointegrate molecule.

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References

  • Arthur A, Sherratt D (1979) Dissection of the transposition process: a transposon-encoded site-specific recombination system. Mol Gen Genet 175:267–274

    Google Scholar 

  • Bachmann B (1972) Pedigrees of some mutant strains of Escherichia coli K-12. Bacteriol Rev 36:525–557

    Google Scholar 

  • Berg DE (1983) Structural requirement for IS50-mediated gene transposition. Proc Natl Acad Sci USA 80:792–796

    Google Scholar 

  • Calos MP, Miller JH (1980) Transposable elements. Cell 20:579–595

    Google Scholar 

  • Chandler M, Clerget M, Galas DJ (1982) The transposition frequency of IS1-flanked transposons is a function of their size. J Mol Biol 154:229–243

    Google Scholar 

  • Chandler M, Roulet E, Silver L, de la Tour EB, Caro L (1979) Tn10-mediated integration of the plasmid R100.1 into the bacterial chromosome: inverse transposition. Mol Gen Genet 173:23–30

    Google Scholar 

  • Chang ACY, Cohen SN (1978) Construction and characterization of amplifiable multicopy DNA cloning vehicles derived from the p15A cryptic miniplasmid. J Bacteriol 134:1141–1156

    Google Scholar 

  • Chopra I, Shales SW, Ward JM, Wallace LJ (1981) Reduced expression of Tn10-mediated tetracycline resistance in Escherichia coli containing more than one copy of the transposon. J Gen Microbiol 126:45–54

    Google Scholar 

  • Crisona NJ, Clark AJ (1977) Increase in conjugational transmission frequency of nonconjugative plasmids. Science 196:186–187

    Google Scholar 

  • Crisona NJ, Nowak JA, Nagaishi H, Clark AJ (1980) Transposon-mediated conjugational transmission of nonconjugative plasmids. J Bactriol 142:701–713

    Google Scholar 

  • Coleman DC, Foster TJ (1981) Analysis of the reduction in expression of tetracycline resistance determined by transposon Tn10 in the multicopy state. Mol Gen Genet 182:171–177

    Google Scholar 

  • Curiale MS, Levy SB (1982) Two complementation groups mediate tetracycline resistance determined by Tn10. J Bacteriol 151:209–215

    Google Scholar 

  • Desmet L, Faelen M, Lefèbre N, Résibois A, Toussaint A, van Gijsegem F (1981) Genetic study of Mu transposition and Mumediated chromosomal rearrangements. Cold Spring Harbor Symp Quant Biol 45:355–363

    Google Scholar 

  • Galas DJ, Chandler M (1981) On the molecular mechanisms of transposition. Proc Natl Acad Sci USA 78:4858–4862

    Google Scholar 

  • Galas DJ, Chandler M (1982) Structure and stability of Tn9-mediated cointegrates. Evidence for two pathways of transposition. J Mol Biol 154:245–272

    Google Scholar 

  • Gill R, Heffron F, Dougan G, Falkow S (1978) Analysis of sequences transposed by complementation of 2 classes of transposition deficient mutants of transposition element Tn3. J Bacteriol 136:797–801

    Google Scholar 

  • Guyer MS (1978) The gamma delta sequence of F is an insertion sequence. J Mol Biol 126:347–365

    Google Scholar 

  • Harayama S, Iino T (1982) A simple method for constructing recA strains in Escherichia coli. Jpn J Genet 57:189–191

    Google Scholar 

  • Harayama S, Palva ET, Hazelbauer GL (1979) Transposon-insertion mutants of Escherichia coli K12 defective in a component common to galactose and ribose chemotaxis. Mol Gen Genet 171:193–203

    Google Scholar 

  • Harayama S, Tsuda M, Iino T (1980) High frequency mobilization of the chromosome of Escherichia coli by a mutant of plasmid RP4 temperature-sensitive for maintenance. Mol Gen Genet 180:47–56

    Google Scholar 

  • Harayama S, Engström P, Wolf-Watz H, Iino T, Hazelbauer GL (1982) Cloning of trg, a gene for a sensory transducer in Escherichia coli. J Bacteriol 152:372–383

    Google Scholar 

  • Harshey RM, Bukhari AI (1981) A mechanism of DNA transposition. Proc Natl Acad Sci USA 78:1090–1094

    Google Scholar 

  • Harshey RM, McKay R, Bukhari AI (1982) DNA intermediates in transposition of phage. Mu. Cell 29:561–571

    Google Scholar 

  • Heffron F (1983) Tn3 and its relatives. In: Shapiro JA (ed) Mobile genetic elements. Academic Press Inc, New York, pp 223–260

    Google Scholar 

  • Hirschel BJ, Galas DJ, Berg DE, Chandler M (1982a) Structure and stability of transposon 5-mediated cointegrates. J Mol Biol 159:557–580

    Google Scholar 

  • Hirschel BJ, Galas DJ, Chandler M (1982b) Cointegrate formation by Tn5, but not transposition is dependent on recA. Proc Natl Acad Sci USA 79:4530–4534

    Google Scholar 

  • Iida S, Meyer J, Arber W (1983) Prokaryotic IS elements. In: Shapiro JA (ed) Mobile genetic elements. Academic Press Inc, New York, pp 159–219

    Google Scholar 

  • Jorgensen RA, Reznikoff WS (1979) Organization of structural and regulatory genes that mediate tetracycline resistance in transposon Tn10. J Bacteriol 138:705–714

    Google Scholar 

  • Jorgensen RA, Berg DE, Allet B, Reznikoff WS (1979) Restriction enzyme cleavage map of Tn10, a transposon which encodes tetracycline resistance. J Bacteriol 137:681–685

    Google Scholar 

  • Kado CI, Liu ST (1981) Rapid procedure for detection and isolation of large and small plasmids. J Bacteriol 145:1365–1373

    Google Scholar 

  • Kahn N, Kolter R, Thomas C, Figurski D, Meyer R, Remaut E, Helinski DR (1979) Plasmid cloning vehicles derived from plasmids ColE1, F, R6K and RK2. In: Wu R (ed) Methods in enzymology, vol 68. Academic Press Inc, New York, pp 268–280

    Google Scholar 

  • Kleckner N (1981) Transposable elements in prokaryotes. Annu Rev Genet 15:341–404

    Google Scholar 

  • Kleckner N, Roth J, Botstein D (1977) Genetic engineering in vivo using translocatable drug-resistance elements. New methods in bacterial genetics. J Mol Biol 116:125–159

    Google Scholar 

  • Kleckner N, Barker DF, Ross DG, Botstein D (1978) Properties of the translocatable tetracline-resistance element Tn10 in Escherichia coli and bacteriophage lambda. Genetics 90:427–461

    Google Scholar 

  • Kleckner N, Reichardt K, Botstein D (1979) Inversions and deletions of the Salmonella chromosome generated by the translocatable tetracycline-resistance element Tn10. J Mol Biol 127:89–115

    Google Scholar 

  • Kopecko DJ, Cohen SN (1975) Site-specific recA-independent recombination between bacterial plasmids: involvement of palindromes at the recombinational loci. Proc Natl Acad Sci USA 72:1373–1377

    Google Scholar 

  • Low B (1973) Rapid mapping of conditional and auxotrophic mutation in Escherichia coli K-12. J Bacteriol 113:798–812

    Google Scholar 

  • Liebart JC, Ghelardini P, Paolozzi L (1982) Conservative integration of bacteriophage Mu DNA into pBR322 plasmid. Proc Natl Acad Sci USA 79:4362–4366

    Google Scholar 

  • Miller JH (1972) Experiments in molecular genetics. Cold Spring Harbor Laboratory, Cold Spring Harbor, New-York

    Google Scholar 

  • Shapiro JA (1979) Molecular model for the transposition and replication of bacteriophage Mu and ether transposable elements. Proc Natl Acad Sci USA 76:1933–1973

    Google Scholar 

  • Sherratt DJ, Arthur A, Burke M (1981) Transposon-specified, sitespecific recombination systems. Cold Spring Harbor Symp Quant Biol 45:275–282

    Google Scholar 

  • Syvanen M, Hopkins JD, Clements M (1982) A new class of mutants in DNA polymerase I that effects gene transposition. J Mol Biol 158:203–212

    Google Scholar 

  • Taylor DP, Greedberg J, Rownd RH (1977) Generation of miniplasmids from copy number mutants of the R plasmid NR1. J Bacteriol 132:986–995

    Google Scholar 

  • Tomizawa J, Ogawa T (1968) Replication of phage lambda DNA. Cold Spring Harbor Symp Quant Biol 33:533–551

    Google Scholar 

  • Ward JM, Grinsted J (1978) Mapping of functions in the R-plasmid R388 by examination of deletion mutants generated in vitro. Gene 3:87–95

    Google Scholar 

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Communicated by K. Isono

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Harayama, S., Oguchi, T. & Iino, T. Does Tn10 transpose via the cointegrate molecule?. Molec. Gen. Genet. 194, 444–450 (1984). https://doi.org/10.1007/BF00425556

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