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Trans-activation and stable integration of the maize transposable element Ds cotransfected with the Ac transposase gene in transgenic rice plants

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Abstract

To develop an efficient gene tagging system in rice, a plasmid was constructed carrying a non-autonomous maize Ds element in the untranslated leader sequence of a hygromycin B resistance gene fused with the 35S promoter of cauliflower mosaic virus. This plasmid was cotransfected by electroporation into rice protoplasts together with a plasmid containing the maize Ac transposase gene transcribed from the 35S promoter. Five lines of evidence obtained from the analyses of hygromycin B-resistant calli, regenerated plants and their progeny showed that the introduced Ds was trans-activated by the Ac transposase gene in rice. (1) Cotransfection of the two plasmids is necessary for generation of hygromycin B resistant transformants. (2) Ds excision sites are detected by Southern blot hybridization. (3) Characteristic sequence alterations are found at Ds excision sites. (4) Newly integrated Ds is detected in the rice genome. (5) Generation of 8 by target duplications is observed at the Ds integration sites on the rice chromosomes. Our results also show that Ds can be trans-activated by the transiently expressed Ac transposase at early stages of protoplast culture and integrated stably into the rice genome, while the cotransfected Ac transposase gene is not integrated. Segregation data from such a transgenic rice plant carrying no Ac transposase gene showed that four Ds copies were stably integrated into three different chromosomes, one of which also contained the functional hph gene restored by Ds excision. The results indicate that a dispersed distribution of Ds throughout genomes not bearing the active Ac transposase gene can be achieved by simultaneous transfection with Ds and the Ac transposase gene.

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References

  • Athma P, Grotewold E, Peterson T (1992) Insertional mutagenesis of the maize P gene by intragenic transposition of Ac. Genetics 131:199–209

    Google Scholar 

  • 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 

  • Becker D, Lütticke R, Li M, Starlinger P (1992) Control of excision frequency of maize transposable element Ds in Petunia protoplasts. Proc Natl Acad Sci USA 89:5552–5556

    Google Scholar 

  • Bennett MD, Smith JB, Heslop-Harrison JS (1982) Nuclear DNA amounts in angiosperms. Proc R Soc Lond [B] 216:179–199

    Google Scholar 

  • Chomczynski P, Sacchi N (1987) Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction. Anal Biochem 162:156–159

    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 

  • Cullis CA (1990) DNA rearrangements in response to environmental stress. Adv Genet 28:73–97

    Google Scholar 

  • Datta SK, Peterhans A, Datta K, Potrykus I (1990) Genetically engineered fertile indica-rice recovered from protoplasts. Bio/ Technology 8:736–740

    Google Scholar 

  • Dooner HK, Keller J, Harper E, Ralston E (1991) Variable patterns of transposition of the maize element Activator in tobacco. Plant Cell 3:473–482

    Google Scholar 

  • Fedoroff NV (1989) Maize transposable elements. In: Berg DE, Howe MM (eds) Mobile DNA. American Society for Microbiology, Washington, DC, pp 375–411

    Google Scholar 

  • Gierl A, Saedler H (1992) Plant-transposable elements and gene tagging. Plant Mol Biol 19:39–49

    Google Scholar 

  • Greenblatt IM (1984) A chromosomal replication pattern deduced from pericarp phenotypes resulting from movements of the transposable element, Modulator, in maize. Genetics 108:471–485

    Google Scholar 

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

    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 

  • Houba-Herin 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 

  • Izawa T, Miyazaki C, Yamamoto M, Terada R, Iida S, Shimamoto K (1991) Introduction and transposition of the maize transposable element Ac in rice (Oryza sativa L.). Mol Gen Genet 227:391–396

    Google Scholar 

  • Kermicle JL, Alleman M, Dellaporta SL (1989) Sequential mutagenesis of a maize gene using the transposable element Dissociation. Genome 31:712–716

    Google Scholar 

  • Kinoshita T (1990) Report of the committee on gene symbolization, nomenclature and linkage groups. Rice Genet Newslett 7:16–50

    Google Scholar 

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

    Google Scholar 

  • Laufs J, Wirtz U, Kammann M, Matzeit V, Schaefer S, Schell J, Czernilofsky AP, Baker B, Gronenborn B (1990) 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

    Google Scholar 

  • Li M-G, Starlinger P (1990) Mutational analysis of the N-terminus of the protein of maize transposable element Ac. Proc Natl Acad Sci USA 87:6044–6048

    Google Scholar 

  • Masterson 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 (1984) The significance of responses of the genome to challenge. Science 226:792–801

    Google Scholar 

  • McCouch SR, Kochert G, Yu ZH, Wang ZY, Khush GS, Coffman WR, Tanksley SD (1988) Molecular mapping of rice chromosomes. Theor Appl Genet 76:815–829

    Google Scholar 

  • Moreno MA, Chen J, Greenblatt I, Dellaporta SL (1992) Reconstitutional mutagenesis of the maize P gene by short-range Ac transposition. Genetics 131:939–956

    Google Scholar 

  • Murai N, Li Z, Kawagoe Y, Hayashimoto A (1991) Transposition of the maize Activator element in transgenic rice plants. Nucleic Acids Res 19:617–622

    Google Scholar 

  • Nishibayashi S (1991) Is the size of the rice genome relatively small? Rice Genet Newslett 8:152–154

    Google Scholar 

  • Osborne BI, Corr CA, Prince JP, Hehl R, Tanksley SD, McCormick S, Baker B (1991) Ac transposition from a T-DNA can generate linked and unlinked clusters of insertions in the tomato genome. Genetics 129:833–844

    Google Scholar 

  • Rommens CMT, van Haaren MJJ, Buchel AS, Mol JNM, van Tunen AJ, Nijkamp HJJ, Hille J (1992) Transactivation of Ds by Ac-transposase gene fusions in tobacco. Mol Gen Genet 231:433–441

    Google Scholar 

  • Sambrook J, Fritsch EF, Maniatis T (1989) Molecular cloning: A laboratory manual, 2nd edn. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, New York

    Google Scholar 

  • Sanger F, Nicklen S, Coulson AR (1977) DNA sequencing with chain-terminating inhibitors. Proc Natl Acad Sci USA 74:5463–5467

    Google Scholar 

  • Shimamoto K, Terada R, Izawa T, Fujimoto H (1989) Fertile transgenic rice plants regenerated from transformed protoplasts. Nature 338:274–276

    Google Scholar 

  • Swinburne J, Balcells J, Scofield SR, Jones JDG, Coupland G (1992) Elevated levels of Activator transposase mRNA are associated with high frequencies of Dissociation excision in Arabidopsis. Plant Cell 4:583–595

    Google Scholar 

  • Tilney-Bassett RAE (1986) Plant chimeras. Edward Arnold, London

    Google Scholar 

  • Walbot V (1992) Strategies for mutagenesis and gene cloning using transposon tagging and T-DNA insertional mutagenesis. Annu Rev Plant Physiol Plant Mol Biol 43:49–82

    Google Scholar 

  • Weil CF, Marillonnet S, Burr B, Wessler SR (1992) Changes in state of the wx-m5 allele of maize are due to intragenic transposition of Ds. Genetics 130:175–185

    Google Scholar 

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Communicated by E. Meyerowitz

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Shimamoto, K., Miyazaki, C., Hashimoto, H. et al. Trans-activation and stable integration of the maize transposable element Ds cotransfected with the Ac transposase gene in transgenic rice plants. Molec. Gen. Genet. 239, 354–360 (1993). https://doi.org/10.1007/BF00276933

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  • DOI: https://doi.org/10.1007/BF00276933

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