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. 1985 Dec;111(4):705–713. doi: 10.1093/genetics/111.4.705

Transposition of Plasmid-Borne Tn10 Elements Does Not Exhibit Simple Length-Dependence

J C Way 1,2, N Kleckner 1,2
PMCID: PMC1202666  PMID: 2998922

Abstract

The transposition frequencies of Tn10 elements from the bacterial chromosome to an F epitome decrease 40% for every kilobase increase in transposon length. The basis for this relationship is not known. We have now examined complemented transposition of defective Tn10 elements off small multicopy plasmids. We find that length dependence in this situation is either reduced or absent, depending on the specific class of transposition events involved. These observations can be interpreted as evidence against the model that chromosomal length dependence occurs because of decay of a transposition-associated replicative complex. This interpretation is consistent with unrelated experiments suggesting that Tn10 transposition is normally nonreplicative. Alternative explanations of length dependence phenomena are discussed.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Chandler M., Clerget M., Galas D. J. The transposition frequency of IS1-flanked transposons is a function of their size. J Mol Biol. 1982 Jan 15;154(2):229–243. doi: 10.1016/0022-2836(82)90062-6. [DOI] [PubMed] [Google Scholar]
  2. Foster T. J., Davis M. A., Roberts D. E., Takeshita K., Kleckner N. Genetic organization of transposon Tn10. Cell. 1981 Jan;23(1):201–213. doi: 10.1016/0092-8674(81)90285-3. [DOI] [PubMed] [Google Scholar]
  3. Guyer M. S., Reed R. R., Steitz J. A., Low K. B. Identification of a sex-factor-affinity site in E. coli as gamma delta. Cold Spring Harb Symp Quant Biol. 1981;45(Pt 1):135–140. doi: 10.1101/sqb.1981.045.01.022. [DOI] [PubMed] [Google Scholar]
  4. Kleckner N., Morisato D., Roberts D., Bender J. Mechanism and regulation of Tn10 transposition. Cold Spring Harb Symp Quant Biol. 1984;49:235–244. doi: 10.1101/sqb.1984.049.01.027. [DOI] [PubMed] [Google Scholar]
  5. Morisato D., Way J. C., Kim H. J., Kleckner N. Tn10 transposase acts preferentially on nearby transposon ends in vivo. Cell. 1983 Mar;32(3):799–807. doi: 10.1016/0092-8674(83)90066-1. [DOI] [PubMed] [Google Scholar]
  6. Thompson B. J., Camien M. N., Warner R. C. Kinetics of branch migration in double-stranded DNA. Proc Natl Acad Sci U S A. 1976 Jul;73(7):2299–2303. doi: 10.1073/pnas.73.7.2299. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Weinert T. A., Derbyshire K. M., Hughson F. M., Grindley N. D. Replicative and conservative transpositional recombination of insertion sequences. Cold Spring Harb Symp Quant Biol. 1984;49:251–260. doi: 10.1101/sqb.1984.049.01.029. [DOI] [PubMed] [Google Scholar]

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