Skip to main content
Log in

Plant chromosome/marker gene fusion assay for study of normal and truncated T-DNA integration events

  • Published:
Molecular and General Genetics MGG Aims and scope Submit manuscript

Summary

During Agrobacterium tumefaciens infection, the T-DNA flanked by 24 by imperfect direct repeats is transferred and stably integrated into the plant chromosome at random positions. Here we measured the frequency with which a promoterless reporter gene is activated after insertion into the Nicotiana tabacum SR1 genome. When adjacent to the right or left T-DNA border sequences, at least 35% of the transformants express the marker gene, suggesting preferential T-DNA insertion (>70%) in transcriptionally active regions of the plant genome. When the promoterless neomycin phosphotransferase II (nptII) gene is located internally in the T-DNA, the activation frequency drops to 1% since gene activation requires T-DNA truncation. These truncation events in the nptII upstream region occur independently of the nature of the upstream sequence and of the T-DNA length. Deletion of the right border region prevents the detection of activated marker genes. Therefore, T-DNA truncation probably occurs after synthesis of a normal T-DNA intermediate during the transfer and/or integration process. In the absence of border regions, expression of the nptII selectable marker directed by the nopaline synthase promoter was detected in 1 out of 105 regenerated calli, suggesting the possibility that any DNA sequence from the Ti plasmid can be transformed into the plant genome, albeit at a low frequency.

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.

Institutional subscriptions

Similar content being viewed by others

References

  • Albright LM, Yanofsky MF, Leroux B, Ma S, Nester EW (1987) Processing of the T-DNA of Agrobacterium tumefaciens generates border nicks and linear, single-stranded T-DNA. J Bacteriol 69:1046–1055

    Google Scholar 

  • Ambros PF, Matzke AJM, Matzke MA (1986) Localization of Agrobacterium rhizogenes T-DNA in plant chromosomes by in situ hybridization. EMBO J 5:2073–2077

    Google Scholar 

  • André D, Colau D, Schell J, Van Montagu M, Hernalsteens J-P (1986) Gene tagging in plants by a T-DNA insertion mutagen that generates APH(3′) II-plant gene fusions. Mol Gen Genet 204:512–518

    Google Scholar 

  • Bakkeren G, Koukolíková-Nicola Z, Grimsley N, Hohn B (1989) Recovery of Agrobacterium tumefaciens T-DNA molecules from whole plants early after transfer. Cell 57:847–857

    Google Scholar 

  • Buchanan-Wollaston V, Passiatore JE, Cannon F (1987) The mob and oriT mobilization functions of a bacterial plasmid promote its transfer to plants. Nature 328:172–175

    Google Scholar 

  • Caplan AB, Van Montagu M, Schell J (1985) Genetic analysis of integration mediated by single T-DNA borders. J Bacteriol 161:655–664

    Google Scholar 

  • Casadaban MJ, Cohen SN (1980) Analysis of gene control signals by DNA fusion and cloning in Escherichia coli. J Mol Biol 138:179–207

    Google Scholar 

  • Christie PJ, Ward JE, Winans SC, Nester EW (1988) The Agrobacterium tumefaciens virE2 gene product is a single-stranded-DNA-binding protein that associates with T-DNA. J Bacteriol 170:2659–2667

    Google Scholar 

  • Chyi YS, Jorgensen RA, Goldstein D, Tanksley SD, Loaiza-Figueroa F (1986) Locations and stability of Agrobacterium-mediated T-DNA insertions in the Lycopersicon genome. Mol Gen Genet 204:64–69

    Google Scholar 

  • Citovsky V, De Vos G, Zambryski P (1988) Single-stranded DNA binding protein encoded by the virE locus of Agrobacterium tumefaciens. Science 240:501–504

    Google Scholar 

  • Das A (1988) Agrobacterium tumefaciens virE operon encodes a single-stranded DNA-binding protein. Proc Natl Acad Sci USA 85:2909–2913

    Google Scholar 

  • De Vos G, De Beuckeleer M, Van Montagu M, Schell J (1981) Restriction endonuclease mapping of the octopine tumor inducing pTiAch5 of Agrobacterium tumefaciens. Plasmid 6:249–253

    Google Scholar 

  • Deblaere R, Bytebier B, De Greve H, Deboeck F, Schell J, Van Montagu M, Leemans J (1985) Efficient octopine Ti plasmid-derived vectors for Agrobacterium-mediated gene transfer to plants. Nucleic Acids Res 13:4777–4788

    Google Scholar 

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

    Google Scholar 

  • Deroles SC, Gardner RC (1988) Analysis of the T-DNA structure in a large number of transgenic petunias generated by Agrobacterium-mediated transformation. Plant Mol Biol 11:365–377

    Google Scholar 

  • Dhaese P, De Greve H, Gielen J, Seurinck J, Van Montagu M, Schell J (1983) Identification of sequences involved in the polyadenylation of higher plant nuclear transcripts using Agrobacterium T-DNA genes as models. EMBO J 2:419–426

    Google Scholar 

  • Dürrenberger F, Crameri A, Hohn B, Koukolíková-Nicola Z (1989) Covalently bound VirD2 protein of Arabidopsis thaliana protects the T-DNA from exonucleolytic degradation. Proc Natl Acad Sci USA 86:9154–9158

    Google Scholar 

  • Gheysen G, Herman L, Breyne P, Van Montagu M, Depicker A (1989) Agrobacterium tumefaciens as a tool for the genetic transformation of plants. In: Butler LO, Harwood C, Moseley BEB (eds) Genetic transformation and expression. Intercept, Andover, pp 151–174

    Google Scholar 

  • Gheysen G, Herman L, Breyne P, Gielen J, Van Montagu M, Depicker A (1990) Cloning and sequence analysis of truncated T-DNA inserts from Nicotiana tabacum. Gene, in press

  • Hain R, Stahel P, Czernilofsky AP, Steinbiss H-H, Herrera-Estrella L, Schell J (1985) Uptake, integration, expression and genetic transmission of a selectable chimaeric gene to plant protoplasts. Mol Gen Genet 199:161–168

    Google Scholar 

  • Heinemann JA, Sprague GF Jr (1989) Bacterial conjugative plasmids mobilize DNA transfer between bacteria and yeast. Nature 340:205–209

    Google Scholar 

  • Hepburn AG, White J (1985) The effect of the right terminal repeat deletion on the oncogenicity of the T-region of pTiT37. Plant Mol Biol 5:3–11

    Google Scholar 

  • Herman LMF, Van Montagu M, Depicker AG (1986) Isolation of tobacco DNA segments with plant promoter activity. Mol Cell Biol 6:4486–4492

    Google Scholar 

  • Herrera-Estrella A, Chen Z-M, Van Montagu M, Wang K (1988) VirD proteins of Agrobacterium tumefaciens are required for the formation of a covalent DNA-protein complex at the 5′ terminus of T-strand molecules. EMBO J 7:4055–4062

    Google Scholar 

  • Herrera-Estrella A, Van Montagu M, Wang K (1990) A bacterial peptide acting as a plant nuclear-targeting signal: the Agrobacterium VirD2 directs β-galactosidase into tobacco nuclei. Proc Natl Acad Sci USA, 87: in press

  • Jen GC, Chilton M-D (1986) The right border region of pTiT37 T-DNA is intrinsically more active than the left border region in promoting T-DNA transformation. Proc Nall Acad Sci USA 83:3895–3899

    Google Scholar 

  • Joos H, Timmerman B, Van Montagu M, Schell J (1983) Genetic analysis of transfer and stabilization of Agrobacterium DNA in plant cells. EMBO J 2:2151–2160

    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 

  • Lemmers M, De Beuckeleer M, Holsters M, Zambryski P, Depicker A, Hernalsteens J-P, Van Montagu M, Schell J (1980) Internal organization, boundaries and integration of Ti-plasmid DNA in nopaline crown gall tumours. J Mol Biol 144:353–376

    Google Scholar 

  • Maniatis T, Fritsch EF, Sambrook J (1982) Molecular cloning, a laboratory manual. Cold Spring Harbor Laboratory, Cold Spring Harbor, New York

    Google Scholar 

  • Mooslehner K, Karls U, Harbers K (1990) Retroviral integration sites in transgenic Mov mice frequently map in the vicinity of transcribed DNA regions. J Virol 64:3056–3058

    Google Scholar 

  • Peralta EG, Hellmiss R, Ream W (1986) Overdrive, a T-DNA transmission enhancer on the A. tumefaciens tumour-inducing plasmid. EMBO J 5:1137–1142

    Google Scholar 

  • Simpson RB, Spielmann A, Margossian L, McKnight TD (1986) A disarmed binary vector from Agrobacterium tumefaciens functions in Agrobacterium rhizogenes. Plant Mol Biol 6:403–415

    Google Scholar 

  • Spielmann A, Simpson RB (1986) T-DNA structure in transgenic tobacco plants with multiple independent integration sites. Mol Gen Genet 205:34–41

    Google Scholar 

  • Stachel SE, Messens E, Van Montagu M, Zambryski P (1985) Identification of the signal molecules produced by wounded plant cells that activate T-DNA transfer in Agrobacterium tumefaciens. Nature 318:624–629

    Google Scholar 

  • Stachel SE, Timmerman B, Zambryski P (1986) Generation of single-stranded T-DNA molecules during the initial stages of TDNA transfer from Agrobacterium tumefaciens to plant cells. Nature 322:706–712

    Google Scholar 

  • Stachel SE, Timmerman B, Zambryski P (1987) Activation of Agrobacterium tumefaciens vir gene expression generates multiple single-stranded T-strand molecules from the pTiA6 T-region: requirements for 5′ virD gene products. EMBO J 6:857–863

    Google Scholar 

  • Teeri T, Herrera-Estrella L, Depicker A, Van Montagu M, Palva ET (1986) Identification of plant promoters in situ by T-DNA-mediated transcriptional fusions to the npt-II gene. EMBO J 5:1755–1760

    Google Scholar 

  • Van Lijsebettens M, Inzé D, Van Montagu M, Schell J (1986) Transformed cell clones as a tool to study T-DNA integration mediated by Agrobacterium tumefaciens. J Mol Biol 188:129–145

    Google Scholar 

  • Wallroth M, Gerats AGM, Rogers SG, Fraley RT, Horsch RB (1986) Chromosomal localization of foreign genes in Petunia hybrida. Mol Gen Genet 202:6–15

    Google Scholar 

  • Wang K, Herrera-Estrella L, Van Montagu M, Zambryski P (1984) Right 25-bp terminus sequences of the nopaline T-DNA is essential for and determines direction of DNA transfer from Agrobacterium to the plant genome. Cell 38:455–462

    Google Scholar 

  • Wang K, Stachel S, Timmerman B, Van Montagu M, Zambryski P (1987) Site-specific nick in the T-DNA border sequence following vir gene expression in Agrobacterium. Science 235:587–591

    Google Scholar 

  • Yanofsky MF, Porter SG, Young C, Albright LM, Gordon MP, Nester EW (1986) The virD operon of Agrobacterium tumefaciens encodes a site-specific endonuclease. Cell 47:471–477

    Google Scholar 

  • Young C, Nester EW (1988) Association of the VirD2 protein with the 5′ end of T strands in Agrobacterium tumefaciens. J Bacteriol 170:3367–3374

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

Communicated by J. Schell

Rights and permissions

Reprints and permissions

About this article

Cite this article

Herman, L., Jacobs, A., Van Montagu, M. et al. Plant chromosome/marker gene fusion assay for study of normal and truncated T-DNA integration events. Molec. Gen. Genet. 224, 248–256 (1990). https://doi.org/10.1007/BF00271558

Download citation

  • Received:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00271558

Key words

Navigation