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Clonal analysis of heterogeneous crown gall tumor tissues induced by wild-type and shooter mutant strains ofAgrobacterium tumefaciens-expression of T-DNA genes

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Summary

Tumors were induced by anAgrobacterium tumefaciens strain with a wild-type octopine Ti plasmid and by shooter mutants with a transposon insertion in the auxin-locus of the T-region. Cloning of isolated axenic tumor tissues revealed that in all cases they consisted of tumor cells (10–26%) next to a majority of normal cells. The tumor clones that had been induced by the strain with the wild-type Ti plasmid all grew as amorphous calli. Tumor, clones induced by a shooter mutant were of two different types. One type of clone grew well on phytohormone-free medium. this type invariably regenerated tumorous shoots abundantly on this medium. The other type of clone only grew after the addition of auxin and cytokinin to the culture medium, but slow growth also took place in the presence of only auxin. This type never regenerated shoots spontaneously. After stimulation by a high level of kinetin, however, a few shoots were also obtained from these clones. One of these shoots, like other tumorous shoots, contained the tumor-specific enzyme octopinesynthase (Ocs), but in contrast to other tumorous shoots formed a root-system.

The expression of T-DNA genes in shoots proliferating from the cloned tumor tissues induced by a mutant with an insertion in the region for transcript tr. 2 was studied by northern blot hybridization. Except for tr.2 the T-DNA transcripts were detected in the tumorous shoots analysed, including the transcript, tr.1 from the auxin-locus and tr.4 from the cytokinin-locus. This shows that the presence of these transcripts, which are assumed to be responsible for the tumorigenic character of tumor cells, does not interfere with the differentiation of shoot cells.

One of the shooty tumor clones (TSO38) showed an unstable character with regard to octopine synthase activity (Ocs±). For, TSO38 and some of its subclones, it was found that only 4% of the regenerated shoots were Ocs+. Northern blot hybridization revealed that the mRNA for octopine synthase was present in extremely low quantity in the population of TSO38 derived shoots.

The finding that it was possible to force shoots from clone TSO38 and from subclone TSO38-23 that were Ocs to become Ocs+, proved that the gene for octopine synthase was present in the Ocs shoots and that this gene showed unstable expression due to regulation at the level of transcription.

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References

  1. Akiyoshi DE, Morris RO, Hinz R, Mischke BS, Kosuge T, Garfinkel DJ, Gordon MP, Nester EW: Cytokinin-auxin balance in crown gall tumors is regulated by specific loci in the T-DNA. Proc Natl Acad Sci USA 80:407–411, 1983.

    Google Scholar 

  2. Aviv H, Leder P: Purification of biologically active globin messenger RNA by chromatography on oligothymidilic acid-cellulose. Proc Natl Acad Sci USA 69:1408–1412, 1972.

    Google Scholar 

  3. Binns AN, Sciaky D, Wood HN: Variation in hormone autonomy and regenerative potential of cells transformed by strain A66 of Agrobacterium tumefaciens. Cell 31:605–612, 1982.

    Google Scholar 

  4. Bomhoff G, Klapwijk PM, Kester HCM, Schilperoort RA, Hernalsteens JP, Schell J: Octopine and nopaline synthesis and breakdown genetically controlled by a plasmid of Agrobacterium tumefaciens. Mol Gen Genet 145:177–181, 1976.

    Google Scholar 

  5. Braun AC: A physiological basis for autonomous growth of crown gall tumor cell. Proc Natl Acad Sci USA 44:344–349, 1958.

    Google Scholar 

  6. Braun AC: A demonstration of the recovery of the crown gall tumor cell with the use of complex tumors of single-cell origin. Proc Natl Acad Sci USA 45:932–938, 1959.

    Google Scholar 

  7. Caboche M, Muller J-F: Use of a medium allowing low cell density growth for in vitro selection experiments: isolation of valine-resistent clones from nitrosoguanidine mutagenized cells and gamma irradiated tobacco plants. In: Sala F, Parisi B, Cella r, Ciferri O, (eds.) Plant cell cultures. Elsevier/North Holland Biomedical Press, 1980.

  8. Chilton M-D, Drummond MH, Merlo DJ, Sciaky D, Montoya AL, Gordon MP, Nester EW: Stable incorporation of plasmid DNA into higher plant cells: the molecular basis of crown gall tumorigenesis. Cell 11:263–271, 1977.

    Google Scholar 

  9. Chilton M-D, Drummond MH, Merlo DJ, Sciaky D: Highly conserved DNA of Ti plasmids overlaps T-DNA maintained in plant tumours. Nature 275:147–149, 1978.

    Google Scholar 

  10. De Greve H, Leemans J, Hernalsteens JP, Thia-Toong L, De Beuckeleer M, Willmitzer L, Otten L, Van Montagu M, Schell J: Regeneration of normal and fertile plants that express octopine synthase, from tobacco crown galls after deletion of tumour-controlling functions. Nature 300:752–755, 1982.

    Google Scholar 

  11. Depicker A, Van Montagu M, Schell J: Homologous DNA sequences in different Ti plasmids are essential for oncogenicity. Nature 275:150–153, 1978.

    Google Scholar 

  12. De Vos, G, De Beuckeleer M, Van Montagu M, and Schell J: Restriction endonuclease mapping of the octopine tumorinducing plasmid pTiAch5 of Agrobacterium tumefaciens. Plasmid 6:249–253, 1981.

    Google Scholar 

  13. Garfinkel DJ, Nester EW: Agrobacterium tumefaciens mutants affected in crown gall tumorigenesis and octopine catabolism. J Bacteriol 144:732–743, 1980.

    Google Scholar 

  14. Garfinkel DJ, Simpson RB, Ream LW, White FF, Gordon MP, Nester EW: Genetic analysis of crown gall: fine structure map of the T-DNA by site-directed mutagenesis Cell 27:143–153, 1981.

    Google Scholar 

  15. Gelvin SB, Thomashow MF, McPherson JC, Gordon MP, Nester EW: Sizes and map positions of several plasmid DNA-encoded transcripts, in octopine-type crown gall tumors. Proc Natl Acad Sci USA 79:76–80, 1982.

    Google Scholar 

  16. 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 

  17. Hooykaas PJJ: The role of plasmid determined, functions in the interaction of Rhizobiaceae with plant cells. A genetic approach. Thesis, Leiden, The Netherlands, 1979.

  18. Hooykaas, PJJ and Schilperoort RA: The molecular genetics of crown gall tumorigenesis. Advances in Genetics 22:210–283, 1983.

    Google Scholar 

  19. Klapwijk PM, Scheulderman T, and Schilperrort RA: Coordinated regulation of octopine degradation and conjugative transfer of Ti plasmids in Agrobacterium tumefaciens: evidence for a common regulatory gene and separate operons. J Bacteriol 136:775–785, 1978.

    Google Scholar 

  20. Koekman BP, Ooms G, Klapwijk PM, and Schilperrort RA: Genetic map of an octopine Ti-plasmid. Plasmid 2:347–357, 1979.

    Google Scholar 

  21. Koekman BP, Hooykaas PJJ, and Schilperoort RA: A functional map of the replicator region of the octopine Ti plasmid. Plasmid 7:119–132, 1982.

    Google Scholar 

  22. Linsmaier EM, and Skoog F: Organic growth factor, requirements of tobacco tissue cultures. Physiol Plant 8: 100–127, 1965.

    Google Scholar 

  23. Meins F Jr, and Lutz J: Tissue specific variation in the cytokinin habituation of cultured tobacco cells. Differentiation 15:1–6, 1979.

    Google Scholar 

  24. Memelink J, Wullems GJ, and Schilperoort RA: Nopaline T-DNA is maintained during regeneration and generative propagation of transformed tobacco plants. Mol Gen Genet 190:516–522, 1983.

    Google Scholar 

  25. Murai N, and Kemp JD: Octopine synthase messenger RNA isolated from sunflower crown gall callus is homologous to the Ti plasmid of Agrobacterium tumefaciens. Proc Natl Acad Sci USA 79:86–90, 1982.

    Google Scholar 

  26. Murashige T, and Skoog F: A revised method for rapid growth-and bioassays with tobacco tissue cultures. Physiol Plant 15:473–497, 1962.

    Google Scholar 

  27. Ooms G, Klapwijk PM, Poulis, JA, Schilperoort RA: Characterization of Tn904 insertions in octopine Ti plasmid mutants of Agrobacterium tumefaciens. J Bacteriol 144:82–91 1980.

    Google Scholar 

  28. Ooms G: Molecular biologic studies on Agrobacterium tumefaciens and crown gall plant tumors. Thesis, Leiden, The Netherlands, 1981.

  29. Ooms G, Hooykaas PJJ, Moolenaar G, and Schilperoort, RA: Crown gall plant tumors of abnormal morphology, induced by Agrobacterium tumefaciens carrying mutated octopine Ti plasmids; analysis of T-DNA functions. Gene 14:33–50, 1981.

    Google Scholar 

  30. Ooms G, Bakker A, Molendijk L, Wullems GJ, Gordon MP, Nester EW, and Schilperoort RA: T-DNA organization in homogeneous and heterogeneous octopine-type crown gall tissues of Nicotiana tabacum. Cell 30:589–597, 1982.

    Google Scholar 

  31. Otten LABM, and Schilperoort, RA: A rapid microscale method for the detection of lysopine and nopaline dehydrogenase activities. Biochim Biophys Acta 527:497–500, 1978.

    Google Scholar 

  32. Petit A, Delhaye S, Tempé J, and Morel G: Recherches sur les guanidines des tissus de crown gall. Mise en évidence d'une relation biochimique spécifique entre les souches d'Agrobacterium tumefaciens et les tumeurs qu'elles, induisent. Physiol Végét 8:205–213, 1970.

    Google Scholar 

  33. Rigby PWJ, Dieckmann M, Rhodes C, and Berg P: Labelling deoxyribonucleic acid to high specific activity in vitro by nick translation with DNA polymerase I. J Mol Biol 113:237–251, 1977.

    Google Scholar 

  34. Sacristan MD, and Melchers G: Regeneration of plants from habituated and Agrobacterium-transformed single cell clones of tobacco. Mol Gen Genet 152:111–117, 1977.

    Google Scholar 

  35. Schröder J, Schröder G, Huisman H, Schilperoort RA, and Schell J: The mRNA for lysopinedehydrogenase in plant tumor cells is complementary to a Ti-plasmid fragment. FEBS Lett 129:166–168, 1981.

    Google Scholar 

  36. Skoog F, Miller CO: Chemical regulation of growth and organ formation in plant tissues cultured in vitro. Symp Soc Exp Biol 11:118–131, 1975.

    Google Scholar 

  37. Southern EM: Detection of specific sequences among DNA fragments separated by gel electrophoresis. J Mol Biol 98:503–517, 1975.

    Google Scholar 

  38. Thomashow, MF, Nutter R, Montoya AL, Gordon MP, and Nester EW: Integration and organization of Ti plasmid sequences in crown gall tumors. Cell 19:729–739, 1980.

    Google Scholar 

  39. Van Larebeke N, Genetello C, Schell J, Schilperoort RA, Hermans AK, Hernalsteens JP and Van Montagu M: Acquisition of tumour-inducing ability by non-oncogenic agrobacteria as a result of plasmid transfer. Nature 255:742–743, 1975.

    Google Scholar 

  40. Van Slogteren GMS, Planqué K, and Lekkerkerk J: Evaluation of parameters affecting the initiation of division of protoplasts of haploid and diploid Nicotiana sylvestris and Nicotiana tabacum. Plant Sci Lett 20:35–45, 1980.

    Google Scholar 

  41. Van Slogteren GMS: Characterization of octopine crown gall tumor cells-A study on the expression of Agrobacterium tumefaciens-derived T-DNA genes. Thesis, Leiden, The Netherlands, 1983.

  42. Watson B, Currier TC, Gordon MP, Chilton M-D, and Nester EW: Plasmid required for virulence of Agrobacterium tumefaciens. J Bacteriol 123:255–264, 1975.

    Google Scholar 

  43. Willmitzer L, Simons G and Schell J: The TL-DNA in octopine crown gall tumours codes for seven well-defined polyadenylated transcripts. EMBO J 1:139–146, 1982.

    Google Scholar 

  44. Willmitzer L, Dhaese P, Schreier PH, Schmalenbach W, Van Montagu M and Schell J: Size, location and polarity of T-DNA-encoded transcripts in nopaline crown gall tumors; common transcripts in octopine and nopaline tumors. Cell 32:1045–1056, 1983.

    Google Scholar 

  45. Wullems GJ, Molendijk L, Ooms G, Schilperoort RA: Retention of tumor markers in F1 progeny plants from in vitro induced octopine and nopaline tumor tissues. Cell 24:719–727, 1981.

    Google Scholar 

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van Slogteren, G.M.S., Hoge, J.H.C., Hooykaas, P.J.J. et al. Clonal analysis of heterogeneous crown gall tumor tissues induced by wild-type and shooter mutant strains ofAgrobacterium tumefaciens-expression of T-DNA genes. Plant Mol Biol 2, 321–333 (1983). https://doi.org/10.1007/BF01578594

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