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Establishment of a gene tagging system in Arabidopsis thaliana based on the maize transposable element Ac

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Summary

An Ac-derived, two-component transposable element system has been developed and analyzed with respect to its use in Arabidopsis thaliana. This system consists of an immobilized Ac element (“Ac clipped wing”, Accl) as the source of transactivating transposase and a nonautonomous “Ds” element, DsA, which is inserted into a chimaeric neomycinphosphotransferase gene used as excision marker. After separate introduction of Acc1 and DsA into Arabidopsis thaliana, progeny analysis of crosses between five different Accl lines and seven different DsA lines shows that: (1) different Accl lines differ greatly in their capacity to transactivate DsA; (2) different DsA lines do not differ significantly with respect to DsA transactivation by one Accl line; (3) reintegration of excised DsA elements, both at (genetically) linked and unlinked sites, occurs in about 50% of the excision events; and (4) plants with a high rate of somatic excisions can be used as source of new DsA transpositions, allowing the creation of a large number of independent DsA insertions.

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References

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

    Google Scholar 

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

    Google Scholar 

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

    Google Scholar 

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

    Google Scholar 

  • Bowman JL, Yanofsky MF, Meyerowitz EM (1988) Arabidopsis thaliana: A Review. Oxf Surv Plant Mol Cell Biol 5:57–87

    Google Scholar 

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

    Google Scholar 

  • DeBlock M, Botterman J, Vandewiele M, Dockx J, Thoen C, Gosselé V, Movva NR, Thompson C, Van Montagu M, Leemans J (1987) Engineering herbicide resistance in plants by expression of a detoxifying enzyme. EMBO J 6:2513–2518

    Google Scholar 

  • Dellaporta SL, Wood J, Hicks JB (1983) A plant DNA minipreparation: version II. Plant Mol Biol Rep 1:19–21

    CAS  Google Scholar 

  • Döring HP, Starlinger P (1984) Barbara McClintock's controlling elements: now at the DNA level. Cell 39:253–259

    Google Scholar 

  • Döring HP, Starlinger P (1986) Molecular genetics of transposable elements in plants. Annu Rev Genet 20:175–200

    Google Scholar 

  • Fedoroff N, Wessier S, Shure M (1983) Isolation of the transposable maize controlling elements Ac and Ds. Cell 35:243–251

    Google Scholar 

  • Fedoroff N, Furtek D, Nelson O (1984) 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

    Google Scholar 

  • Feinberg AP, Vogelstein B (1983) A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity. Anal Biochem 132:6–13

    Google Scholar 

  • Feldman KA, Marks MD (1987) Agrobacterium-mediated transformation of germinating seeds of Arabidopsis thaliana: A non tissue-culture approach. Mol Gen Genet 208:1–9

    Google Scholar 

  • Feldman KA, Marks MD, Christianson ML, Quatrano RS (1989) A dwarf mutant of Arabidopsis generated by T-DNA insertion mutagenesis. Science 243:1351–1354

    Google Scholar 

  • Feldman KA, Carlson TJ, Coomber SA, Farrance CE, Mandel MA, Wierzbicki AM (1990) T-DNA insertional mutagenesis in Arabidopsis thaliana. In: Bennet AB, O'Neill SD (eds) Horticultural biotechnology. Wiley-Liss, New York, pp 109–120

    Google Scholar 

  • Hake S, Vollbrecht E, Freeling M (1989) Cloning Knotted, the dominant morphological mutant in maize using Ds2 as a transposon tag. EMBO J 8:15–22

    Google Scholar 

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

    Google Scholar 

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

    Google Scholar 

  • Houba-Hérin N, Becker D, Post A, Larondelle Y, Starlinger P (1990) 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

    Google Scholar 

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

    Google Scholar 

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

    Google Scholar 

  • Koncz C, Martini N, Mayerhofer R, Koncz-Kalman Z, Körber H, Redei GP, Schell J (1989) High-frequency T-DNA-mediated gene tagging in plants. Proc Natl Acad Sci USA 86:8467–8471

    Google Scholar 

  • Koncz C, Meyerhofer R, Koncz-Kalman Z, Nawrath C, Reiss B, Redei GP, Schell J (1990) Isolation of a gene encoding a novel chloroplast protein by T-DNA tagging in Arabidopsis thaliana. EMBO J 9:1337–1346

    Google Scholar 

  • Larkin PJ, Scowcroft WR (1981) Somaclonal variation — a novel source of variability from cell cultures for plant improvement. Theor Appl Genet 60:197–214

    Google Scholar 

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

    Google Scholar 

  • Maniatis T, Fritsch EF, Sambrook J (1982) Molecular cloning. A laboratory manual. Cold Spring Harbor Laboratory Press Cold Spring Harbor, N.Y.

    Google Scholar 

  • Marks MD, Feldman KA (1989) Trichome development in Arabidopsis thaliana. I. T-DNA tagging of the GLABROUS1 gene. Plant Cell 1:1043–1050

    Google Scholar 

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

    Google Scholar 

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

    Google Scholar 

  • McClintock B (1951) Chromosome organization and genic expression. Cold Spring Harbor Symp Quant Biol 16:13–47

    Google Scholar 

  • McClintock B (1952) Mutable loci in maize. Carnegie Inst Washington Yearb 51:212–219

    Google Scholar 

  • Meyerowitz EM (1989) Arabidopsis, a useful weed. Cell 56:263–269

    Google Scholar 

  • Motto M, Maddaloni M, Ponziani G, Brembilla M, Marotta R, Di Fonzo N, Soave C, Thompson R, Salamini F (1988) Molecular cloning of the o2-m5 allele of Zea mays using transposon marking. Mol Gen Genet 212:488–494

    Google Scholar 

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

    Google Scholar 

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

    Google Scholar 

  • Nakamaye KL, Eckstein F (1986) Inhibition of restriction endonuclease NciI cleavage by phosphothioate groups and its application to olidonucleotide-directed mutagenesis. Nucleic Acids Res 14:9679–9698

    Google Scholar 

  • Nevers P, Shepherd NS, Saedler H (1986) Plant transposable elements. Adv Bot Res 12:103–203

    Google Scholar 

  • Otten LEABM, Schilperoort RA (1978) A rapid micro scale method for the detection of lysopine and nopaline dehydrogenase activities. Biochim Biophys Acta 527:497–500

    Google Scholar 

  • Peleman J, Cottyn B, Van Camp W, Van Montagu M, Inzé D (1991) Transient occurrence of extrachromosomal DNA of an Arabidopsis thaliana transposon-like element, Tatl. Proc Natl Acad Sci USA 88:3618–3622

    Google Scholar 

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

    Google Scholar 

  • Rédei GP (1975) Arabidopsis as a genetic tool. Annu Rev Genet 9:111–127

    Google Scholar 

  • Reiss B, Sprengel R, Will H, Schaller H (1984) A new sensitive method for the qualitative and quantitative assay of neomycin phosphotransferase in crude cell extracts. Gene 30:211–218

    Google Scholar 

  • Schmidt R, Willmitzer L (1988) High efficiency Agrobacterium tumefaciens-mediated transformation of Arabidopsis thaliana leaf and cotyledon expiants. Plant Cell Rep 7:583–586

    Google Scholar 

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

    Google Scholar 

  • Schmidt R, Willmitzer L (1990) Ac transposition in Arabidopsis thaliana. Schweizer D, Peuker K, Loidl J (eds), University of Vienna, Vienna. In: 4th Int Conf Arabidopsis Res. Vienna, p 21 (abstr)

  • Taylor JW, Ott J, Eckstein F (1985) The rapid generation of oligonucleotide-directed mutations at high frequency using phosphothioate-modified DNA. Nucleic Acids Res 13:8765–8785

    Google Scholar 

  • Theres N, Scheele T, Starlinger P (1987) Cloning of the Bz2 locus of Zea mays using the transposable element Ds as a tag. Mol Gen Genet 209:193–197

    Google Scholar 

  • Thompson CJ, Movva NR, Tizard R, Crameri R, Davies JE, Lauwereys M, Botterman J (1987) Characterization of the herbicide resistance gene bar from Streptomyces hygroscopicus. EMBO J 6:2519–2523

    Google Scholar 

  • Van Haute E, Joos H, Maes M, Warren G, Van Montagu M, Shell J (1983) Intergenic transfer and exchange recombination of restriction fragments cloned in pBR322: a novel strategy for reversed genetics of the Ti plasmids of Agrobacterium tumefaciens. EMBO J 2:411–417

    Google Scholar 

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

    Google Scholar 

  • von Schaewen A (1989) Untersuchungen zur ER-vermittelten, subzellulären Kompartimentierung fremder Proteine in höheren Pflanzen. Ph. D. thesis, Freie Universität Berlin, Berlin, FRG

    Google Scholar 

  • Yanofsky MF, Ma H, Bowman JL, Drews GN, Feldman KA, Meyerowitz EM (1990) The protein encoded by the Arabidopsis homeotic gene agamous resembles transcription factors. Nature 346:35–38

    Google Scholar 

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

    Google Scholar 

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Communicated by G. Wenzel

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Altmann, T., Schmidt, R. & Willmitzer, L. Establishment of a gene tagging system in Arabidopsis thaliana based on the maize transposable element Ac . Theoret. Appl. Genetics 84, 371–383 (1992). https://doi.org/10.1007/BF00229496

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  • DOI: https://doi.org/10.1007/BF00229496

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