Skip to main content
Log in

Development and characterization of a generalized gene tagging system for higher plants using an engineered maize transposon Ac

  • Research Article
  • Published:
Plant Molecular Biology Aims and scope Submit manuscript

Abstract

This report describes a series of transposon tagging vectors for dicotyledonous plants based on the maize transposable element Ac. This binary system includes the transposase (Ts) and the tagging element (Ds) on separate T-DNA vectors. Ts elements include versions in which transcription is driven either by the endogenous Ac promoter or by the cauliflower mosaic virus (CaMV) 35S promoter. Ds tagging element includes a gene conferring methotrexate (Mtx) resistance for selection and a supF gene to facilitate cloning of tagged sequences. The Ds element is flanked by a CaMV 35S promoter and the β-glucuronidase (GUS) coding sequence so that GUS expression occurs upon excision of the element. We have transformed these Ts and Ds elements into tobacco and demonstrated that the Ts is functional with either promoter, and that the artificial Ds elements are capable of transposition. The amount of excision was found to depend upon both the individual Ts and Ds primary transformants used. Somatic excision of Ds was seen in up to 100% of progeny seedlings containing Ts and Ds. Germinal excision was detected in up to 48% of the progeny of plants containing both elements. Hence, this system can generate a sufficient number of events to be useful in gene tagging.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. An G, Watson BD, Chiang CC: Transformation of tobacco, tomato, potato and Arabidopsis thaliana using a binary Ti vector system. Plant Physiol 81: 301–305 (1986).

    Google Scholar 

  2. Baker B, Coupland G, Fedoroff N, Starlinger P, Schell J: Phenotypic assay for excision of the maize controlling element Ac in tobacco. EMBO J 6: 1547–1554 (1987).

    Google Scholar 

  3. Baker B, Schell J, Lörz H, Fedoroff N: Transposition of the maize controlling element ‘Activator’ in tobacco. Proc Natl Acad Sci USA 83: 4844–4848 (1986).

    Google Scholar 

  4. Behrens U, Fedoroff N, Laird A, Müller-Neumann M, Starlinger P, Yoder J: Cloning of the Zea mays controlling element Ac from the wx-m7 allele. Mol Gen Genet 194: 346–347 (1984).

    Google Scholar 

  5. Belzile F, Lassner MW, Tong Y, Khush R, Yoder JI: Sexual transmission of transposed Activator elements in transgenic tomatoes. Genetics 123: 181–189 (1989).

    Google Scholar 

  6. Bevan M: Binary Agrobacterium vectors for plant transformation. Nucl Acids Res 12: 8711–8721 (1984).

    Google Scholar 

  7. Bingham PM, Levis R, Rubin GM: Cloning of cDNA sequences from the white locus of D. melanogaster by a novel and general method. Cell 25: 693–704 (1981).

    Google Scholar 

  8. Birnboim: A rapid alkaline extraction method for the isolation of plasmid DNA. Meth Enzymol 100: 243–255 (1983).

    Google Scholar 

  9. Chaleff RS: Genetics of Higher Plants: Application of Cell Cultures. Cambridge University Press, Cambridge (1981), 184 pp.

    Google Scholar 

  10. Coupland G, Baker B, Schell J, Starlinger P: Characterization of the maize transposable element Ac by internal deletions. EMBO J 7: 3653–3659 (1988).

    Google Scholar 

  11. Coupland G, Plum C, Chatterjee S, Post A, Starlinger P: Sequences near the termini are required for transposition of the maize transposon Ac in transgenic tobacco plants. Proc Natl Acad Sci USA 86: 9385–9388 (1989).

    Google Scholar 

  12. Depicker A, Herman L, Jacobs A, Schell J, VanMontagu M: Frequencies of simultaneous transformation with different T-DNAs and their relevance to the Agrobacterium/plant cell interaction. Mol Gen Genet 201: 477–484 (1985).

    Google Scholar 

  13. Eichholtz DA, Rogers SG, Horsch RB, Klee HJ, Hayford M, Hoffmann NL, Braford SB, Fink C, Flick J, O'Connell KM, Fraley RT: Expression of mouse dihydrofolate reductase gene confers methotrexate resistance in transgenic petunia plants. Somatic Cell Mol Genet 13: 67–76 (1987).

    Google Scholar 

  14. Fedoroff NV, Furtek DB, Nelson OE: Cloning of the bronze locus in maize by a simple and generalizable procedure using the transposable controlling element Activator (Ac). Proc Natl Acad Sci USA 81: 3825–3829 (1984).

    Google Scholar 

  15. Finnegan EJ, Taylor BH, Craig S, Dennis ES: Transposable elements can be used to study cell lineages in transgenic plants. Plant Cell 1: 757–764 (1989).

    Google Scholar 

  16. Haring MA, Rommens CMT, Nijkamp HJJ, Hille J: The use of transgenic plants to understand transposition mechanisms and to develop transposon tagging strategies. Plant Mol Biol 16: 449–461 (1991).

    Google Scholar 

  17. Hehl R, Baker B: Induced transposition of Ds by a stable Ac in crosses of transgenic tobacco plants. Mol Gen Genet 217: 53–59 (1989).

    Google Scholar 

  18. Hehl R, Baker B: Properties of the maize transposable element Activator in transgenic tobacco plants: A versatile inter-species genetic tool. Plant Cell 2: 709–721 (1990).

    Google Scholar 

  19. Hoekema A, Hirsch PR, Hooykaas PJJ, Schilperoort RA: A binary plant vector strategy based on separation of vir-and T-region of the Agrobacterium tumefaciens Ti-plasmid. Nature 303: 179–180 (1983).

    Google Scholar 

  20. Holsters M, deWaele D, Depicker A, Messens E, VanMontagu M, Schell J: Transfection and transformation of Agrobacterium tumefaciens. Mol Gen Genet 163: 181–187 (1978).

    Google Scholar 

  21. Houba-Hérin N, Becker D, Post A, Larondelle Y, Starlinger P: Excision of a Ds-like maize transposable element (AcΔ) in a transient assay in Petunia is enhanced by a truncated coding region of the transposable element Ac. Mol Gen Genet 224: 17–23 (1990).

    Google Scholar 

  22. Jefferson RA, Kavanagh TA, Bevan MW: GUS fusions: β-glucuronidase as a sensitive and versatile gene fusion marker in higher plants. EMBO J 6: 3901–3907 (1987).

    Google Scholar 

  23. Jones JDG, Carland F, Lim E, Ralston E, Dooner HK: Preferential transposition of the maize element Activator to linked chrosomal locations in tobacco. Plant Cell 2: 701–707 (1990).

    Google Scholar 

  24. Jones JDG, Carland FM, Maliga P, Dooner HK: Visual detection of transposition of the maize element Activator (Ac) in tobacco seedlings. Science 244: 204–207 (1989).

    Google Scholar 

  25. Knapp S, Coupland G, Uhrig H, Starlinger P, Salamini F: Transposition of the maize transposable element Ac in Solanum tuberosum. Mol Gen Genet 213: 285–290 (1988).

    Google Scholar 

  26. Kunkel TA, Roberts JD, Zakour RA: Rapid and efficient site-specific mutagenesis without phenotypic selection. Meth Enzymol 154: 367–382 (1987).

    Google Scholar 

  27. Kunze R, Stochaj U, Laufs J, Starlinger P: Transcription of transposable element Activator (Ac) of Zea mays L. EMBO J 6: 1555–1563 (1987).

    Google Scholar 

  28. Lassner MW, Palys JM, Yoder JI: Genetic transactivation of Dissociation elements in transgenic tomato plants. Mol Gen Genet 218: 25–32 (1989).

    Google Scholar 

  29. Laufs J, Wirtz U, Kammann M, Matzeit V, Schaefer S, Schell J, Czernilofsky AP, Baker B, Gronenborn B: Wheat dwarf virus Ac/Ds vectors: Expression and excision of transposable elements introduced into various cereals by a viral replicon. Proc Natl Acad Sci USA 87: 7752–7756 (1990).

    Google Scholar 

  30. Mandel M, Higa A: Calcium dependent bacteriophage DNA infection. J Mol Biol 53: 159–162 (1970).

    Google Scholar 

  31. Maniatis T, Fritsch EF, Sambrook J: Molecular Cloning: A Laboratory Manual. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY (1982).

    Google Scholar 

  32. Martin C, Carpenter R, Sommer H, Saedler H, Coen E: Molecular analysis of instability in flower pigmentation of Antirrhinum majus, following isolation of the pallida locus by transposon tagging. EMBO J 4: 1625–1630 (1985).

    Google Scholar 

  33. Masson P, Fedoroff NV: Mobility of the maize Suppressor mutator element in transgenic tobacco cells. Proc Natl Acad Sci USA 86: 2219–2223 (1989).

    Google Scholar 

  34. Masterson RV, Furtek DB, Grevelding C, Schell J: A maize Ds transposable element containing a dihydrofolate reductase gene transposes in Nicotiana tabacum and Arabidopsis thaliana. Mol Gen Genet 219: 461–466 (1989).

    Google Scholar 

  35. Morelle G: A plasmid extraction procedure on a miniprep scale. Focus 11: 7–8 (1989).

    Google Scholar 

  36. Müller-Neumann M, Yoder JI, Starlinger P: The DNA sequence of the transposable element Ac of Zea mays L. Mol Gen Genet 198: 19–24 (1984).

    Google Scholar 

  37. Murashige T, Skoog F: A revised medium for rapid growth and bioassays with tobacco tissue cultures. Physiol Plant 15: 473–497 (1962).

    Google Scholar 

  38. Nagy JI, Maliga P: Streptomycin-resistant plants from callus culture of haploid tobacco. Z Pflanzenphysiol 78: 453–455 (1976).

    Google Scholar 

  39. Odell J, Caimi P, Sauer B, Russell S: Site-directed recombination in the genome of transgenic tobacco. Mol Gen Genet 223: 369–378 (1990).

    Google Scholar 

  40. Pohlman R, Fedoroff NV, Messing J: The nucleotide sequence of the maize controlling element Activator. Cell 37: 635–643 (1984).

    Google Scholar 

  41. Schmidt R, Willmitzer L: The maize autonomous element Activator (Ac) shows a minimal germinal excision frequency of 0.2%–0.5% in transgenic Arabidopsis thaliana plants. Mol Gen Genet 220: 17–24 (1989).

    Google Scholar 

  42. Seed B: Purification of genomic sequences from bacteriophage libraries by recombination and selection in vivo. Nucl Acids Res 11: 2427–2445 (1983).

    Google Scholar 

  43. Simonsen CC, Levinson AD: Isolation and expression of an altered mouse dihydrofolate reductase cDNA. Proc Natl Acad Sci USA 80: 2495–2499 (1983).

    Google Scholar 

  44. Taylor BH, Finnegan EJ, Dennis ES, Peacock WJ: The maize transposable element Ac excises in progeny of transformed tobacco. Plant Mol Biol 13: 109–118 (1989).

    Google Scholar 

  45. VanSluys MA, Tempé J, Fedoroff N: Studies on the introduction and mobility of the maize Activator element in Arabidopsis thaliana and Daucus carota. EMBO J 6: 3881–3889 (1987).

    Google Scholar 

  46. Yanisch-Perron C, Vieira J, Messing J: Improved M13 phage cloning vectors and host strains: nucleotide sequences of the M13mp18 and pUC19 vectors. Gene 33: 103–119 (1985).

    Google Scholar 

  47. Yoder JI, Palys J, Alpert K, Lassner M: Ac transposition in transgenic tomato plants. Mol Gen Genet 213: 291–296 (1988).

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Fitzmaurice, W.P., Lehman, L.J., Nguyen, L.V. et al. Development and characterization of a generalized gene tagging system for higher plants using an engineered maize transposon Ac . Plant Mol Biol 20, 177–198 (1992). https://doi.org/10.1007/BF00014487

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00014487

Key words

Navigation