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Interaction between the Tam1 and Tam2 transposable elements of Antirrhinum majus

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Summary

Two stable derivatives of the highly unstable niv-53::Tam1 allele of Antirrhinum majus were analysed. In both derivatives the Tam1 element is integrated at the same site and in the same orientation as in the parental niv-53::Tam1 allele. In both cases the Tam1 element was found to carry a 5 bp deletion (CACTA) in one of its termini. This explains the excision deficiency of these two alleles of Tam1, niv-53::Tam1-46 and niv-53::Tam1-49. Niv-44::Tam2, another stable nivea mutation, carries the 5 kb element Tam2, which is not a derivative of Tam1 but possesses identical terminal inverted repeats. When the stable lines 46 and 49 were corssed with line 44, suprisingly, a high number of the flowers in the F1 displayed a variegated phenotype. Sequence analysis of two germinal revertants isolated from the heterozygote niv-53::Tam1-46/niv-44::Tam2 shows excision of the Tam2 element. This indicates that Tam2 is a defective element, which can be complemented by an active Tam1 element. However, the variegated F1 phenotype observed is not inherited monofactorially. Variegation is seen only at particular times of development of the F1 plants. These phenomena seem to involve both the Tam1 and Tam2 transposable elements.

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References

  • Benton WD, Davis RW (1977) Screening lambda gt recombinant clones by hybridization to single plaques in situ. Science 196:180–182

    Google Scholar 

  • Bonas U, Sommer H, Harrison BJ, Saedler H (1984a) The transposable element Tam1 of Antirrhinum majus is 17 kb long. Mol Gen Genet 194:138–143

    Google Scholar 

  • Bonas U, Sommer H, Saedler H (1984b) The 17-kb Tam1 element of Antirrhinum majus induces a 3-bp duplication upon integration into the chalcone synthase gene. EMBO J 3:1015–1019

    Google Scholar 

  • Breathnach R, Chambon P (1981) Organization and expression of eucaryotic split genes coding for proteins. Annu Rev Biochem 50:349–383

    Google Scholar 

  • Carpenter R, Coen ES, Hudson AD, Martin CR (1984) Transposable elements and genetic instability in Antirrhinum. John Innes Annual Report. Norwich, England

  • Harrison BJ, Carpenter R (1973) A comparison of the instabilities at the nivea and pallida loci in Antirrhinum majus. Heredity 31:309–323

    Google Scholar 

  • Hohn B (1979) In vitro packaging of lambda and cosmid DNA. Methods Enzymol 68:299

    Google Scholar 

  • Holmes DS, Quigley M (1981) A rapid boiling method for the preparation of bacterial plasmids. Anal Biochem 114:193–197

    Google Scholar 

  • Hudson A, Carpenter R, Coen ES (1987) The de novo activation of the transposable element Tam2 of Antirrhinum majus. Mol Gen Genet 207:54–59

    Google Scholar 

  • Kuckuck H (1936) Über vier neue Serien multipler Allele bei Antirrhinum majus. Z Inductive Abstammungs Vererbungslehre 71:429–440

    Google Scholar 

  • Maxam AM, Gilbert W (1980) Sequencing end-labeled DNA with base-specific chemical cleavages. Methods Enzymol 65:499–560

    Google Scholar 

  • Meinkoth J, Wahl G (1984) Hybridization of nucleic acids on solid supports. Anal Biochem 138:267–284

    Google Scholar 

  • Mount SM (1982) A catalogue of splice junction sequences. Nucleic Acids Res 10:459–472

    Google Scholar 

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

    Google Scholar 

  • Murray NE (1983) Phage lambda and molecular cloning. In: Hendrix RW, Roberts JW, Stahl FW, Weisberg RA (eds) Lambda II. Cold Spring Harbor Laboratory, Cold Spring Harbor, New York, pp 395–432

    Google Scholar 

  • Nevers P, Shepherd NS, Seadler H (1985) Plant transposable elements Adv Bot Res 12:102–203

    Google Scholar 

  • Norrander J, Kempe T, Messing J (1983) Construction of improved M13 vectors using oligonucleotide-directed mutagenesis. Gene 26:101–106

    Google Scholar 

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

    Google Scholar 

  • Saedler H, Nevers P (1985) Transposition in plants: a molecular model. EMBO J 4:585–590

    Google Scholar 

  • Schwarz-Sommer Zs, Gierl A, Berndtgen R, Saedler H (1985) Sequence comparison of ‘states’ of a1-m1 suggests a model of Spm (En) action. EMBO J 4:2439–2443

    Google Scholar 

  • Schwarz-Sommer Zs, Gierl A, Klösgen RB, Wienand U, Peterson PA, Saedler H (1984) The Spm (En) transposable element controls the excision of a 2-kb DNA insert at the wxm-8 allele of Zea mays. EMBO J 3:1021–1028

    Google Scholar 

  • Sommer H, Saedler H (1986) Structure of the chalcone synthase gene of Antirrhinum majus. Mol Gen Genet 202:429–434

    Google Scholar 

  • Sommer H, Carpenter R, Harrison BJ, Saedler H (1985a) The transposable element Tam3 of Antirrhinum majus generates a novel type of sequence alteration upon excision. Mol Gen Genet 199:225–231

    Google Scholar 

  • Sommer H, Krebbers E, Piotrowiak R, Bonas U, Hehl R, Saedler H (1985b) Transposable elements of Antirrhinum majus. In: Freeling M (ed), UCLA symposia on molecular and cellular biology, New series, vol 35, Plant genetics. Alan R. Liss, pp 433–444

  • Southern EM (1975) Detection of specific sequences among DNA fragments separated by gel electrophoresis. J Mol Biol 98:503–571

    Google Scholar 

  • Spribille R, Forkmann G (1982) Genetic control of chalcone synthase activity in flowers of Antirrhinum majus. Phytochem 21:2231–2234

    Google Scholar 

  • Sutton W, Gerlach WL, Schwartz D, Peacock WJ (1984) Molecular analysis of Ds controlling element mutations at the Adh1 locus of Zea mays. Science 223:1265–1268

    Google Scholar 

  • Tacke E, Schwarz-Sommer Zs, Peterson PA, Saedler H (1986) Molecular analysis of states of the a1 locus of Zea mays. Maydica 31:83–91

    Google Scholar 

  • Upadhyaya KC, Sommer H, Krebbers E, Saedler H (1985) The paramutagenic line niv-44 has a 5 kb insert, Tam2, in the chalcone synthase gene of Antirrhinum majus. Mol Gen Genet 199:201–207

    Google Scholar 

  • Vieira J, Messing J (1982) The uPC plasmids, and M13mp7-derived system for insertion mutagenesis and sequencing with synthetic universal primers. Gene 19:259–268

    Google Scholar 

  • Wienand U, Sommer H, Schwarz Zs, Shepherd N, Saedler H, Kreuzaler F, Ragg H, Hahlbrock K, Harrison BJ, Peterson PA (1982) A general method to identify plant structural genes among genomic DNA clones using transposable element induced mutations. Mol Gen Genet 187:195–201

    Google Scholar 

  • Yamamoto KR, Alberts BM, Benzinger R, lawhorne L, Treiber G (1970) Rapid bacteriophage sedimentation in the presence of polyethylene glycol and its application to large-scale virus purification. Virology 40:734–744

    Google Scholar 

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Communicated by J. Schell

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Hehl, R., Sommer, H. & Saedler, H. Interaction between the Tam1 and Tam2 transposable elements of Antirrhinum majus . Mol Gen Genet 207, 47–53 (1987). https://doi.org/10.1007/BF00331489

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  • DOI: https://doi.org/10.1007/BF00331489

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