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Part of the book series: Results and Problems in Cell Differentiation ((RESULTS,volume 12))

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Abstract

Recent advances in plant tissue culture techniques, recombinant DNA technology, and bacterial genetics, have made it feasible to isolate specific genes, manipulate them in vitro, and introduce them into plant cells. This not only opens up the exciting possibility of genetically manipulating crop plants, but also provides a powerful tool for studying regulation of plant gene expression and, possibly, for molecular cloning of selectable plant genes from gene libraries. Transformation, in this review, refers to the stable introduction of foreign genetic material into cells. There are several potential plant transformation vectors, DNA vehicles required for the efficient introduction and replication of foreign genes in cells (reviewed by Howell 1982). However, only the Ti-plasmid, the casual agent of crown gall tumorigenesis and, to a much more limited extent, the cauliflower mosaic virus (CaMV) have been successfully used to propagate foreign sequences in plants.

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References

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

    Google Scholar 

  • Albinger G, Beiderbeck R (1977) Übertragung der Fähigkeit zur Wurzelinduktion von Agrobacterium rhizogenes auf A. tumefaciens. Phytopathol Z 90: 306–310

    Google Scholar 

  • Amasino RM, Miller CO (1982) Hormonal control of tobacco crown gall tumor morphology. Plant Physiol (Bethesda) 69: 389–392

    CAS  Google Scholar 

  • Armour SL, Melcher U, Pirone TP, Lyttle DJ, Essenberg RC (1983) Helper component for aphid transmission encoded by region II of cauliflower mosaic virus DNA. Virology 129: 25–30

    PubMed  CAS  Google Scholar 

  • Balazs E, Guilley H, Jonard G, Richards K (1982) Nucleotide sequence of DNA from an altered- virulence isolate D/H of cauliflower mosaic virus. Gene (Amst) 19: 239–249

    CAS  Google Scholar 

  • Banerjee D, Basu M, Choudhary I, Chatterjee GC (1981) Cell surface carbohydrates of Agrobacterium tumefaciens involved in adherence during crown gall tumor initiation. Biochem Biophys Res Commun 100: 1384–1388

    PubMed  CAS  Google Scholar 

  • Barker RF, Idler KB, Thompson DV, Kemp JD (1983) Nucleotide sequence of the T-DNA region from the Agrobacterium tumefaciens octopine Ti plasmid pTi15955. Plant Mol Biol 2: 335–350

    CAS  Google Scholar 

  • Barry GF, Roger SG, Fraley RT, Brand L (1984, in press) Identification of a cloned cytokinin biosynthetic gene. Gene (Amst)

    Google Scholar 

  • Barton KA, Chilton MD (1983) Agrobacterium Ti-plasmids as vectors for plant genetic engineering. In: Wu R, Grossman L, Moldave K (eds) Recombinant DNA, part C. Methods in Enzymology, Vol 101. Academic, New York, pp 527–539

    Google Scholar 

  • Barton KA, Binns AN, Matzke AJM, Chilton M-D (1983) Regeneration of intact tobacco plants containing full length copies of genetically engineered T-DNA, and transmission of T-DNA to R1 progeny. Cell 32: 1033–1043

    PubMed  CAS  Google Scholar 

  • Benoist C, O’Hare K, Breathnach R, Chambon P (1980) The ovalbumin gene sequence of putative control regions. Nucleic Acids Res 8: 127–142

    PubMed  CAS  Google Scholar 

  • Bevan M, Chilton M-D (1982 a) Multiple transcripts of T-DNA detected in nopaline crown gall tumors. J Mol Appl Genet 1: 539–546

    Google Scholar 

  • Bevan MW, Chilton M-D (1982 b) T-DNA of the Agrobacterium Ti and Ri plasmids. Annu Rev Genet 16: 357–384

    Google Scholar 

  • Bevan M, Barnes WM, Chilton M-D (1983 a) Structure and transcription of the nopaline synthase gene region of T-DNA. Nucleic Acids Res 11: 369–385

    Google Scholar 

  • Bevan MW, Flavell RB, Chilton M-D (1983 b) A chimeric antibiotic resistance gene as a selectable marker for plant cell transformation. Nature (Lond) 304: 184–184

    Google Scholar 

  • Binns AN (1984, in press) The biology and molecular biology of plant cells infected by Agrobacterium tumefaciens. In: Miffin B (ed) Oxford surveys of plant molecular and cell biology, vol 1. Oxford Univ Press, London

    Google Scholar 

  • Binns AN, Wood HN, Braun AC (1981) Suppression of the tumorous state in crown gall teratomas of tobacco: A clonal analysis. Differentiation 19: 97–102

    Google Scholar 

  • Binns AN, Sciaky D, Wood HN (1982) Variation in hormone autonomy and regenerative po- tential of cells transformed by strain A66 of Agrobacterium tumefaciens. Cell 31: 605–612

    PubMed  CAS  Google Scholar 

  • Braun AC (1952) Conditioning of the host cell as a factor in the transformation process. Growth 16: 65–74

    PubMed  CAS  Google Scholar 

  • Braun AC (1982) A history of the crown gall problems. In: Kahl G, Schell J (eds) Molecular biology of plant tumors. Academic, New York, pp 155–210

    Google Scholar 

  • Braun AC, Wood HN (1976) Suppression of the neoplastic state with the acquisition of specialized functions in cells, tissues, and organs of crown gall teratomas of tobacco. Proc Natl Acad Sci USA 73: 496–500

    PubMed  CAS  Google Scholar 

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

    PubMed  CAS  Google Scholar 

  • Broglie R, Coruzzi G, Fraley RT, Rogers SG, Horsch RB, Niedermeyer JG, Fink CL, Flick JS

    Google Scholar 

  • Chua N-H (1984) Light-regulated expression of a pea ribulose-1,5-bisphosphate carboxylase small subunit gene in transformed plant cells. Science (Wash DC) 224: 838–843

    Google Scholar 

  • Calos MP, Miller JH (1980) Transposable elements. Cell 20: 579–595

    PubMed  CAS  Google Scholar 

  • Caplan A, Herrera-Estrella L, Inze D, Van Haute E, Van Montagu M, Schell J, Zambryski P (1983) Introduction of genetic material into plant cells. Science (Wash DC) 222: 815–821

    CAS  Google Scholar 

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

    Google Scholar 

  • Chilton M-D, Drummond MH, Merlo DJ, Sciaky D (1978) Highly conserved DNA of Ti plas-mids overlaps T-DNA maintained in plant tumors. Nature (Lond) 275: 147–149

    CAS  Google Scholar 

  • Chilton M-D, Tepfer DA, Petit A, David CC, Delbert F, Tempe J (1982) Agrobacterium rhizo-genes inserts T-DNA into plant roots. Nature (Lond) 295: 432–434

    Google Scholar 

  • Chilton WS, Tempe J, Matzke M, Chilton M-D (1984) Succinamopine: a new crown gall opine. J Bacteriol 157: 357–362

    PubMed  CAS  Google Scholar 

  • Comai L, Schilling-Cordaro C, Mergia A, Houck CH (1983) A new technique for genetic engineering of Agrobacterium Ti-plasmid. Plasmid 10: 21–30

    PubMed  CAS  Google Scholar 

  • Covey SN, Hull R (1981) Transcription of cauliflower mosaic virus DNA: Detection of transcripts, properties and location of the gene encoding the virus inclusion body protein. Virology 11: 463–474

    Google Scholar 

  • Daubert S, Richins R, Shepherd RJ, Gardner RC (1982) Mapping of the coat protein gene of cauliflower mosaic virus by its expression in a prokaryotic system. Virology 122: 444–449

    PubMed  CAS  Google Scholar 

  • Daubert S, Shepherd RJ, Gardner RC (1983) Insertional mutagenesis of the cauliflower mosaic virus genome. Gene (Amst) 25: 201–208

    CAS  Google Scholar 

  • Davey MR, Cocking EC, Freeman N, Pearce N, Tudor I (1980) Transformation of Petunia protoplasts by isolated Agrobacterium plasmid. Plant Sci Lett 18: 307

    CAS  Google Scholar 

  • David C, Chilton M-D, Tempe J (1984) Conservation of T-DNA in plants regenerated from hairy root cultures. Biotechnology 2: 73–76

    CAS  Google Scholar 

  • De Beuckleer M, Lemmers M, De Vos G, Willmitzer L, Van Monntagu M, Schell J (1981) Fur-ther insight on the transferred-DNA of octopine crown gall. Mol Gen Genet 183: 283–288

    Google Scholar 

  • De Cleene M, De Ley J (1976) The host range of crown gall. Bot Rev 42: 389–466

    Google Scholar 

  • De Cleene M, De Ley JD (1981) The host range of infectious hairy-root. Bot Rev 47:147–194 de Framond A, Barton K, Chilton MD (1983) Mini-Ti: A new strategy for plant genetic engi-neering. Biotechnology 1: 262–269

    Google Scholar 

  • De Greve H, Decraemer H, Seurinck J, Van Montagu M, Schell J (1981) The functional orga- nization of the octopine Agrobacterium tumefaciens plasmid pTiB6S3. Plasmid 6: 235–248

    PubMed  Google Scholar 

  • De Greve H, Leemans J, Hernalsteens JP, Thia-Toong L, De Beuckeleer L, Willmitzer L, Otten L, Van Moutagu M, Schell J (1982) Regeneration of normal and fertile plants that express octopine synthasa, from tobacco crown galls after deletion of tumor-controlling functions. Nature (Lond) 300: 752–755

    Google Scholar 

  • De Greve H, Dhaese P, Seurinck J, Lemmers M, Van Montagu M, Schell J (1983) Nucleotide sequence and transcript map of the Agrobacterium tumefaciens Ti-plasmid-encoded octopine synthase gene. J Mol Appl Genet 1: 499–511

    Google Scholar 

  • Depicker A, Stachel S, Dhaese P, Zambryski P, Goodman HM (1982) Nopaline synthase: transcript mapping and DNA sequence. J Mol Appl Genet 1: 561–574

    PubMed  CAS  Google Scholar 

  • Depicker A, Van Montagu M, Schell J (1983) Plant cell transformation by Agrobacterium plasmids. In: Kosuge T, Meredith CP, Hollaender A (eds) Genetic engineering of plants. Plenum, New York, pp 143–176

    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

    PubMed  CAS  Google Scholar 

  • Dixon LK, Koenig I, Hohn T (1983) Mutagenesis of cauliflower mosaic virus. Gene (Amst) 25: 189–199

    CAS  Google Scholar 

  • Draper J, Davey MR, Freeman JP, Cocking EC, Cox BJ (1982) Ti-plasmid homologous sequences present in tissues from Agrobacterium plasmid-transformed Petunia protoplasts. Plant Cell Physiol 23: 451–458

    CAS  Google Scholar 

  • Dudley KR, Odell JT, Howell SH (1982) Structure and 5’-termini of the large and 19S RNA transcripts encoded by the cauliflower mosaic virus genome. Virology 117: 19–28

    PubMed  CAS  Google Scholar 

  • Ellis JG, Murphy PH (1981) Four new opines from crown gall tumors — their detection and properties. Mol Gen Genet 181: 36–43

    CAS  Google Scholar 

  • Engler G, Depicker A, Maenhout R, Villarroel R, Van Montagu M, Schell J (1981) Physical mapping of DNA base sequence homologies between an octopine and a nopaline Ti-plasmid of Agrobacterium tumefaciens. J Mol Biol 152: 183–208

    CAS  Google Scholar 

  • Fraley RT, Horsch RB (1983) In vitro plant transformation systems using liposomes and bacterial co-cultivation. In: Kosuge T, Meredith CP, Hollaender A (eds) Genetic engineering of plants. Plenum, New York, pp 177–194

    Google Scholar 

  • Fraley RT, Rogers SG, Horsch RB, Sanders PR, Flick JS, Adams SP, Bittner ML, Brand LA, Fink CL, Fry JS, Gallupi GR, Goldberg SB, Hoffmann NL, Woo SC (1983) Expression of bacterial genes in plant cells. Proc Natl Acad Sci USA 80: 4803–4807

    PubMed  CAS  Google Scholar 

  • Franck A, Guilley H, Jonard G, Richards K, Hirth L (1980) Nucleotide sequences of cauliflower mosaic virus DNA. Cell 21: 285–294

    PubMed  CAS  Google Scholar 

  • Furusawa I, Yamaoka N, Okuno T, Yamamoto M, Kohno M, Kunoh H (1980) Infection of turnip protoplasts with cauliflower mosaic virus. J Gen Virol 48: 431–435

    Google Scholar 

  • Gardner RC (1983) Plant viral vectors: CaMV as an experimental tool. In: Kosuge T, Meredith CP, Hollaender A (eds) Genetic engineering of plants. Plenum, New York, pp 121–142

    Google Scholar 

  • Gardner R, Howarth A, Hahn P, Brown-Leudi M, Shepherd R, Messing J (1981) The complete nucleotide sequence of an infectious clone of cauliflower mosaic virus by Ml3mp7 shotgun sequencing. Nucleic Acids Res 9: 2871–2888

    PubMed  CAS  Google Scholar 

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

    Google Scholar 

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

    PubMed  CAS  Google Scholar 

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

    PubMed  CAS  Google Scholar 

  • Gelvin SB, Karchner Si, DiRita VJ, Talierco EW (1983) Transcription of the Ti-plasmid in crown gall tumors. In: Pühler A (ed) Molecular genetics of the bacteria-plant interaction. Springer, Berlin Heidelberg New York, pp 292–302

    Google Scholar 

  • Gielen J, De Beuckleer M, Seurinck J, Deboeck F, DeGreve H, Lemmers M, Van Montagu M, Schell J (1984) The complete nucleotide sequence of the TL-DNA of the Agrobacterium tumefaciens plasmid pTiAch5. EMBO J 3: 835–846

    PubMed  CAS  Google Scholar 

  • Givord L, Xiong C, Giband M, Koenig I, Hohn T, Lebeurier G, Hirth L (1984) A second cauliflower mosaic virus gene product influences the structure of the viral inclusion body. EMBO J 3: 1423–1427

    PubMed  CAS  Google Scholar 

  • Gronenborn B, Gardner R, Schaefer S, Shepherd R (1981) Propagation of foreign DNA in plants using CaMV as a vector. Nature (Lond) 294: 773–775

    CAS  Google Scholar 

  • Guilfoyle TJ (1980) Transcription of the cauliflower mosaic virus genome in isolated nuclei from turnip leaves. Virology 107: 71–80

    PubMed  CAS  Google Scholar 

  • Guilley H, Dudley RK, Jonard G, Balazs E, Richards KE (1982) Transcription of cauliflower mosaic virus DNA: detection of promoter sequences, and characterization of transcripts. Cell 30: 763–773

    PubMed  CAS  Google Scholar 

  • Guilley H, Richards KE, Jonard G (1983) Observations concerning the discontinuous DNA’s of cauliflower mosaic virus. EMBO J 2: 277–282

    PubMed  CAS  Google Scholar 

  • Gunge N (1983) Yeast DNA plasmids. Annu Rev Microbiol 37: 253–276

    PubMed  CAS  Google Scholar 

  • Hamilton WDO, Bisaro DM, Coutts RHA, Buck KW (1983) Demonstration of the bipartite nature of the genome of a single-stranded DNA plant virus by infection with the cloned DNA components. Nucleic Acids Res 11: 7387–7396

    PubMed  CAS  Google Scholar 

  • Hasezawa S, Nagata T, Syono K (1981) Transformation of Vinca protoplasts midiated by Agro-bacterium spheroplasts. Mol Gen Genet 182: 206–210

    Google Scholar 

  • Helmer G, Casadaban M, Bevan M, Kayes L, Chilton M-D (1984) A new chimeric gene as a marker for plant transformation: the expression of Escherichia coli ß-galactosidase in sunflower and tobacco cells. Biotechnology 2: 500–507

    Google Scholar 

  • Hepburn AG, Clarke LE, Blundy KS, White J (1983a) Nopaline Ti-plasmid, pTiT37, T-DNA insertions into a flax genome. J Mol Appl Genet 2: 211–224

    Google Scholar 

  • Hepburn AG, Clarke LE, Pearson L, Blundy KS, White J ( 1983 b) The fate of T-DNA in flax. In: Chater KF, Cullis CA, Hopwood DA, Johnston AAWB, Woolhouse HW (eds) Genetic rearrangement. Sinauer, Sunderland, Mass, pp 169–181

    Google Scholar 

  • Hernalsteens JP, Van Vliet F, De Beuckleer M, Depicker A, Engler G, Lemmers M, Holsters M, Van Montagu M, Schell J (1980) The Agrobacterium tumefaciens Ti-plasmid as a host vector system for introducing foreign DNA in plant cells. Nature (Lond) 287: 654–656

    CAS  Google Scholar 

  • Herrera-Estrella L, De Block M, Messens E, Hernalsteens J-P, Van Montagu M, Schell J (1983 a) Chimeric genes as dominant selectable markers in plant cells. EMBO J 2: 987–995

    Google Scholar 

  • Herrera-Estrella L, Depicker A, Van Montagu M, Schell J (1983 b) Expression of chimeric genes transferred into plant cells using a Ti-plasmid-derived vector. Nature (Lond) 303: 209–213

    Google Scholar 

  • Hille J, Klasen I, Schilperoort R (1982) Construction and application of R prime plasmids, carrying different segments of an octopine Ti-plasmid from Agrobacterium tumefaciens for complementation of vir genes. Plasmid 7: 107–118

    PubMed  CAS  Google Scholar 

  • Hille J, Wullems G, Schilperoort R (1983) Non-oncogenic T-region mutants of Agrobacterium tumefaciens do transfer T-DNA into plant cells. Plant Mol Biol 2: 155–163

    CAS  Google Scholar 

  • Hille J, Van Kan J, Schilperoort R (1984) Trans-acting virulence functions of the octopine Ti plasmid from Agrobacterium tumefaciens. J Bacteriol 158: 754–756

    PubMed  CAS  Google Scholar 

  • Hoekema A, Hirsch PR, Hooykaas PJJ, Schilperoort RA (1983) A binary plant vector strategy based on separation of vir-and T-region of the Agrobacterium tumefaciens Ti-plasmid. Nature (Lond) 303: 179–180

    CAS  Google Scholar 

  • Hoekema A, Hooykaas PJ, Schilperoort RA (1984) Transfer of the octopine T-DNA segment to plant cells mediated by different types of Agrobacterium tumor-or root-inducing plasmids: generality of virulence systems. J Bacteriol 158: 383–385

    PubMed  CAS  Google Scholar 

  • Hohn B, Hohn T (1982) Cauliflower mosaic virus: a potential vector for plant genetic engineering. In: Kahl G, Schell J (eds) Molecular biology of plant tumors. Academic, New York, pp 549–560

    Google Scholar 

  • Hohn T, Richards K, Lebeurier G (1982) Cauliflower mosaic virus on its way to becoming a useful plant vector. In: Hofschneider PH, Goebel W (eds) Gene cloning in organisms other than E. coli. Curr Top Microbiol Immunol, vol 96. Springer, Berlin Heidelberg New York, pp 193–236

    Google Scholar 

  • Holsters M, Silva B, Van Vliet F, Genetello C, De Block M, Dhaese P, Depicker A, Inze D, Engler G, Villarroel R, Van Montagu M, Schell J (1980) The functional organization of the nopaline A. tumefaciens plasmid pTiC58. Plasmid 3: 212–230

    PubMed  CAS  Google Scholar 

  • Holsters M, Villaroel R, Van Montagu M, Schell J (1982) The use of selectable markers for the isolation of plant DNA/T-DNA junction fragments in a vector. Mol Gen Genet 185: 283–289

    CAS  Google Scholar 

  • Holsters M, Villarroel R, Gielen J, Seurinck J, De Greve H, Van Montagu M, Schell J (1983) An analysis of the boundaries of the octopine TL-DNA in tumors induced by Agrobacterium tumefaciens. Mol Gen Genet 190: 35–41

    CAS  Google Scholar 

  • Hooykaas PJJ, Schilperoort RA (1984) The molecular genetics of crown gall tumorigenesis. In: Scandalios JG (ed) Molecular genetics of plants. Adv Genet, vol 22. Academic Press, Orlando, pp 209–283

    Google Scholar 

  • Horsch RB, Fraley RT, Rogers SG, Sanders PR, Lloyd A, Hoffmann N (1984) Inheritance of functional foreign genes in plants. Science (Wash DC) 223: 496–498

    CAS  Google Scholar 

  • Howarth AJ, Goodman RM (1982) Plant viruses with genomes of single-stranded DNA. Trends Biochem Sci 7: 180–182

    CAS  Google Scholar 

  • Howell SH (1982) Plant molecular vehicles: potential vectors for introducing foreign DNA into plants. Annu Rev Plant Physiol 33: 609–650

    CAS  Google Scholar 

  • Howell SH, Hull R (1978) Replication of cauliflower mosaic virus and transcription of its genome in turnip leaf protoplasts. Virology 86: 468–481

    PubMed  CAS  Google Scholar 

  • Howell SH, Walker LL, Dudley RK (1980) Cloned cauliflower mosaic virus DNA infects turnips (Brassica rapa). Science (Wash DC) 208: 1265–1267

    CAS  Google Scholar 

  • Howell S, Walker L, Walden R (1981) Rescue of in vitro generated mutants of cloned CaMV genome in infected plants. Nature (Lond) 293: 485–486

    Google Scholar 

  • Hull R, Covey SN (1983) Characterization of cauliflower mosaic virus DNA forms isolated from infected turnip leaves. Nucleic Acids Res 11: 1881–1895

    PubMed  CAS  Google Scholar 

  • Inze D, Follin A, Van Lijsebettens M, Simeons C, Gentello C, Van Montagu M, Schell J (1984) Genetic analysis of the individual T-DNA genes of Agrobacterium tumefaciens; further evidence that two genes are involved in indole-3-acetic acid synthesis. Mol Gen Genet 194: 265274

    Google Scholar 

  • Iyer UN, Klee HJ, Nester EW (1982) Units of genetic expression in the virulence region of a plant tumor-inducing plasmid of Agrobacterium tumefaciens. Mol Gen Genet 188: 418–424

    PubMed  CAS  Google Scholar 

  • Joos H, Inze D, Caplan A, Sormann M, Van Montagu M, Schell J (1983 a) Genetic analysis of T-DNA transcripts in nopaline crown galls. Cell 32: 1057–1067

    Google Scholar 

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

    Google Scholar 

  • Kahl G, Schell J (eds) (1982) Molecular biology of plant tumors. Academic, New York Karchner SJ, DiRita VJ, Gelvin SB (1984) Transcript analysis of TRDNA in octopine-type crown gall tumors. Mol Gen Genet 194: 159–165

    Google Scholar 

  • Kemp JD (1982) Enzymes in octopine and nopaline metabolism. In: Kahl G, Schell J (eds) Molecular biology of plant tumors. Academic, New York, pp 461–474

    Google Scholar 

  • Kemp JD (1983) Genetic engineering of plants by novel approaches. In: Inouye M (ed) Experimental manipulation of gene expression. Academic, New York, pp 119–135

    Google Scholar 

  • Kerr A, Ellis JG (1982) Conjugation and transfer of Ti-plasmids in Agrobacterium tumefaciens. In: Kahl G, Schell J (eds) Molecular biology of plant tumors. Academic, New York, pp 321344

    Google Scholar 

  • Klapwijk PM, Scheulderman T, Schilperoort RA (1978) Coordinate regulations 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

    PubMed  CAS  Google Scholar 

  • Klee HJ, Gordon MP, Nester EW (1982) Complementation analysis of oncogenicity. J Bacteriol 150: 327–331

    PubMed  CAS  Google Scholar 

  • Klee H, Montoya A, Horodyski F, Lichtenstein C, Garfinkel D, Fuller S, Flores C, Peschon J, Nester E, Gordon M (1984) Nucleotide sequence of the tms genes of the pTiA6NC octopine Ti-plasmid: two gene products involved in plant tumorigenesis. Proc Natl Acad Sci USA 81: 1728–1732

    PubMed  CAS  Google Scholar 

  • Koekman BP, Ooms G, Klapwijk PM, Schilperoort RA (1979) Genetic map of an octopine Tiplasmid. Plasmid 2: 347–357

    PubMed  CAS  Google Scholar 

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

    PubMed  CAS  Google Scholar 

  • Koncz C, De Greve H, Andre D, Deboeck F, Van Montagu M, Schell J (1983) The opine synthase genes carried by Ti-plasmids contain all signals necessary for expression in plants. EMBO J 2: 1597–1603

    PubMed  CAS  Google Scholar 

  • Koncz C, Kreuzaler F, Kalman ZS, Schell J (1984) A simple method to transfer, integrate and study expression of foreign genes, such as chicken ovalbumin and a-actin in plant tumors. EMBO J 5: 1029–1037

    Google Scholar 

  • Krens FA, Molendijk L, Wullens GJ, Schilperoort RA (1982) In vitro transformation of plant protoplasts with Ti-plasmid DNA. Nature (Lond) 296: 72–74

    CAS  Google Scholar 

  • Lahners K, Byrne MC, Chilton M-D (1984) T-DNA fragments of hairy root plasmid pRi8196 are distantly related to octopine and nopaline Ti-plasmid T-DNA. Plasmid 11: 130–140

    PubMed  CAS  Google Scholar 

  • Landy A, Ross W (1977) Viral integration and excision: structure of the lambda att sites. Science (Wash DC) 197: 1147–1159

    CAS  Google Scholar 

  • Lebeurier G, Hirth L, Hohn T, Hohn B (1980) Infectivities of native and cloned DNA of cauliflower mosaic virus. Gene (Amst) 12: 139–146

    CAS  Google Scholar 

  • Lebeurier G, Hirth L, Hohn B, Hohn T (1982) In vivo recombination of cauliflower mosaic virus DNA. Proc Natl Acad Sci USA 79: 2932–2936

    PubMed  CAS  Google Scholar 

  • Leemans J, Shaw C, Deblaere R, De Greve H, Hernalsteens JP, Maes M, Van Montagu M, Schell J (1981) Site-specific mutagenesis of Agrobacterium Ti-plasmids and transfer of genes to plant cells. J Mol Appl Genet 1: 149–164

    PubMed  CAS  Google Scholar 

  • Leemans J, Deblaere R, Willmitzer L, De Greve H, Hernalsteens JP, Van Montagu M, Schell J (1982) Genetic identification of functions of TL-DNA transcripts in octopine crown galls. EMBO J 1: 147–152

    PubMed  CAS  Google Scholar 

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

    PubMed  CAS  Google Scholar 

  • Lichtenstein C, Klee H, Montoya A, Garfinkel D, Fuller S, Flores C, Nester E, Gordon M (1984) Nucleotide sequence and transcript mapping of the tmr gene of the pTiA6NC octopine Tiplasmid: a bacterial gene involved in plant tumorigenesis. J Mol Appl Genet 2: 354–362

    PubMed  CAS  Google Scholar 

  • Lipetz J (1966) Crown gall tumorigenesis. II. Relations between wound healing and the tumorigenic response. Cancer Res 26: 1597–1604

    PubMed  CAS  Google Scholar 

  • Liu ST, Perry KL, Schandl CL, Kado CI (1982) Agrobacterium Ti-plasmid indoleacetic acid geneis required for crown gall oncogenesis. Proc Natl Acad Sci USA 79: 2812–2816

    Google Scholar 

  • Lundquist RC, Close TJ, Kado CL (1984) Genetic complementation of Agrobacterium tumefa-ciens Ti plasmid mutants in the virulence region. Mol Gen Genet 193: 1–7

    PubMed  CAS  Google Scholar 

  • Marton L, Wullems GJ, Molendijk L, Schilperoort RA (1979) In vitro transformation of cultured cells from Nicotiana tabacum by Agrobacterium tumefaciens. Nature (Lond) 277: 129–131

    Google Scholar 

  • Matthysee AG (1983) The use of tissue cultures in the study of crown gall and other bacterial diseases. In: Hegelson JP, Deverall BJ (eds) Use of tissue culture and protoplasts in plant pathology. Academic, Sydney, pp 51–68

    Google Scholar 

  • Matzke AJM, Chilton M-D (1981) Site-specific insertion of genes into T-DNA of the Agrobacterium tumor-inducing plasmid: an approach to genetic engineering of higher plant cells. J Mol Appl Genet 1: 39–49

    PubMed  CAS  Google Scholar 

  • Maule AJ (1983) Infection of protoplasts from several Brassica species with cauliflower mosaic virus following inoculation using polyethylene glycol. J Gen Virol 64: 2655–2660

    Google Scholar 

  • McPherson JC, Nester EW, Gordon MP (1980) Proteins encoded by Agrobacterium tumefaciens Ti-plasmid DNA ( T-DNA) in crown gall tumors. Proc Natl Acad Sci USA 77: 2666–2670

    Google Scholar 

  • Meins F (1982) Habituation of cultured plant cells. In: Kahl G, Schell J (eds) Molecular biology of plant tumors. Academic, New York, pp 3–31

    Google Scholar 

  • Memelink J, Wullems GJ, Schilperoort RA (1983) Nopaline T-DNA retained during regenera- tion and generative propagation of transformed plants. Mol Gen Genet 190: 516–522

    CAS  Google Scholar 

  • Murai N, Kemp JD (1982 a) T-DNA of pTi15955 from Agrobacterium tumefaciens is transcribed into a minimum of seven polyadenylated RNAs in a sunflower crown gall tumor. Nucleic Acids Res 10: 1679–1689

    Google Scholar 

  • Murai N, Kemp JD (1982 b) 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

    Google Scholar 

  • Murai N, Sutton D, Murray M, Slightom J, Merlo D, Reichert N, Sengupta-Gopalan C, Stock C, Barker R, Kemp J, Hall T (1983) Phaseolin gene from bean is expressed after transfer to sunflower via tumor-inducing plasmid vectors. Science (Wash DC) 222: 476–481

    CAS  Google Scholar 

  • Nagata T (1983) Liposomes as a carrier of Ti-plasmid into protoplasts. In: Pühler A (ed) Molecular genetics of the bacteria-plant interaction. Springer, Berlin Heidelberg New York, pp 268–273

    Google Scholar 

  • Nakajima H, Yakota T, Matsumoto T, Noguchi M, Takahashi N (1979) Relationship between hormone content and autonomy in various autonomous tobacco cells cultured in suspension. Plant Cell Physiol 29: 1489–1499

    Google Scholar 

  • Odell J, Howell S (1980) Identification, mapping and characterization of mRNA for P66, a CaMV-coded protein. Virology 102: 439–359

    Google Scholar 

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

    PubMed  CAS  Google Scholar 

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

    CAS  Google Scholar 

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

    Google Scholar 

  • Ooms G, Mulendijk L, Schilperoort RA (1982 b) Double infection of tobacco plants two complementing octopine T-region mutants of Agrobacterium tumefaciens. Plant Mol Biol 1: 217–226

    Google Scholar 

  • Otten LABM, Vreugdenhil D, Schilperoort RA (1977) Properties of D(+) lysopine dehydrogenase from crown gall tumour tissue. Biochim Biophys Acta 485: 268–277

    PubMed  CAS  Google Scholar 

  • Otten L, De Greve H, Hernalsteens JP, Van Montagu M, Schieder O, Straub J, Schell J (1981) Mendelian transmission of genes introduced into plants by the Ti-plasmids of Agrobacterium tumefaciens. Mol Gen Genet 183: 209–213

    PubMed  CAS  Google Scholar 

  • Petit A, David C, Dahl GA, Ellis JP, Guyon P, Casse-Delbart F, Tempe J (1983) Further extension of the opine concept: plasmids in Agrobacterium rhizogenes cooperate for opine degradation. Mol Gen Genet 190: 204–214

    CAS  Google Scholar 

  • Pfeiffer P, Hohn T (1983) Involvement of reverse transcription in the replication of the plant virus CaMV: a detailed model and test of some aspects. Cell 33: 781–784

    PubMed  CAS  Google Scholar 

  • Rao SS, Lippincott BB, Lippincott JA (1982) Agrobacterium adherence involves the pectic portion of the host cell wall and is sensitive to the degree of pectin methylation. Physiol Plant 56: 374–380

    Google Scholar 

  • Ream LW, Gordon MP (1982) Crown gall disease and prospects for genetic manipulation of plants. Science (Wash DC) 218: 854–859

    CAS  Google Scholar 

  • Ream LW, Gordon MP, Nester EW (1983) Multiple mutations in the T-region of Agrobacterium tumefaciens tumor-inducing plasmid. Proc Natl Acad Sci USA 80: 1660–1664

    PubMed  CAS  Google Scholar 

  • Rigby PWJ (1983) Cloning vectors derived from animal viruses. J Gen Virol 64:255–266

    PubMed  CAS  Google Scholar 

  • Risuleo G, Battistoni P, Constantino P (1982) Regions of homology between tumorigenic plas-mids from Agrobacterium rhizogenes and Agrobacterium tumefaciens. Plasmid 7: 45–51

    PubMed  CAS  Google Scholar 

  • Rosenberg M, Court D (1979) Regulatory sequences involved in the promotion and termination of RNA transcription. Annu Rev Genet 13: 319–353

    PubMed  CAS  Google Scholar 

  • Ruvkun GB, Ausubel FM (1981) A general method for site directed mutagenesis in prokarystes. Nature (Lond) 289: 85–88

    CAS  Google Scholar 

  • Sacristan MD, Melchers G (1977) Regeneration of plants from “habituated” and “Agrobac-terium-transformed” single cell clones of tobacco. Mol Gen Genet 152: 111–117

    Google Scholar 

  • Salomon F, Deblaere R, Leemans J, Hernalsteens J-P, Van Montagu M, Schell J (1984) Geneticidentification of functions of TR-DNA transcripts in octopne crown galls. EMBO J 3: 141–146

    PubMed  CAS  Google Scholar 

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

    Google Scholar 

  • Schröder G, Schröder J (1982) Hybridization selection and translation of T-DNA encoded in RNAs from octopine tumors. Mol Gen Genet 185: 52–55

    Google Scholar 

  • Schröder G, Klipp W, Hillebrand A, Ehring R, Koncz C, Schröder J (1983) The conserved part of the T-region in Ti-plasmids expresses four proteins in bacteria. EMBO J 2: 403–409

    PubMed  Google Scholar 

  • Schröder G, Waffenschmidt S, Weiler EW, Schröder J (1984) The T-region of Ti-plasmids codes for an enzyme synthesizing indole-3-acetic acid. Eur J Biochem 138: 387–391

    PubMed  Google Scholar 

  • Shaw CH, Leemans J, Shaw CH, Van Montagu M, Schell J (1983) A general method for the transfer of cloned genes to plant cells. Gene (Amst) 23: 315–330

    CAS  Google Scholar 

  • Simpson RB, O’Hara Pi, Kwok W, Montoya AM, Lichtenstein C, Gordon MP, Nester EW (1982) DNA from the A6 S/2 crown gall tumor contains scrambled Ti-plasmid sequences near its junctions with plant DNA. Cell 29: 1005–1014

    PubMed  CAS  Google Scholar 

  • Skoog F, Miller CO (1957) Chemical regulation of growth and organ formation in plant tissues cultured in vitro. Symp Soc Exp Biol 11: 118–131

    PubMed  CAS  Google Scholar 

  • Smith GR (1983) Chi hotspots of generalized recombination. Cell 34: 709–710

    PubMed  CAS  Google Scholar 

  • Sutton WD, Gerlach WL, Schwartz D, Peacock WJ (1984) Molecular analysis of Ds controlling element mutations at the Adh 1 locus of maize. Science (Wash DC) 223: 1265–1268

    CAS  Google Scholar 

  • Tate ME, Ellis JG, Kerr A, Tempe J, Murray KE, Shaw KJ (1982) Agropine: a revised structure. Carbohydr Res 104: 105–120

    CAS  Google Scholar 

  • Temin HM (1980) Origin of retroviruses from cellular movable genetic elements. Cell 21: 599–600

    PubMed  CAS  Google Scholar 

  • Tempe J, Petit A, Holsters M, Van Montagu M, Schell J (1977) Thermosensitive step associated with transfer of the Ti-plasmid during conjugation: possible relation to transformation in crown gall. Proc Natl Acad Sci USA 74: 2848–2849

    PubMed  CAS  Google Scholar 

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

    PubMed  CAS  Google Scholar 

  • Thomashow MF, Nutter R, Postle K, Chilton M-D, Blattner FR, Powell A, Gordon MP, Nester EW (1980b) Recombination between higher plant DNA and the Ti plasmid of Agrobacterium tumefaciens. Proc Natl Acad Sci USA 77: 6448–6452

    PubMed  CAS  Google Scholar 

  • Thomashow MF, Knauf VC, Nester EW (1981) The relationship between the limited and wide host range octopine type Ti plasmids of Agrobacterium tumefaciens. J Bacteriol 146: 484–493

    PubMed  CAS  Google Scholar 

  • Toh H, Hayashida H, Miyata T (1983) Sequence homology between retroviral reverse transcriptase and putative polymerases of hepatitis B virus and cauliflower mosaic virus. Nature (Lond) 305: 827–829

    CAS  Google Scholar 

  • Turgeon R (1982) Teratomas and secondary tumors. In: Kahl G, Schell J (eds) Molecular biology of plant tumors. Academic, New York, pp 391–414

    Google Scholar 

  • Turgeon R, Wood HN, Braun AC (1976) Studies on the recovery of crown gall tumor cells. Proc Natl Acad Sci USA 73: 3562–3564

    PubMed  CAS  Google Scholar 

  • Urisic D, Slighton J L, Kemp JD (1983) Agrobacterium tumefaciens T-DNA integrates into multiple sites of sunflower crown gall genome. Mol Gen Genet 190: 494–508

    Google Scholar 

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

    PubMed  Google Scholar 

  • Van Larebeke N, Engler G, Holsters M, Van den Elsacker S, Zaenen I, Schilperoort RA, Schell J (1974) Large plasmid in Agrobacterium tumefaciens essential for crown-gall inducing ability. Nature (Lond) 252: 169–170

    Google Scholar 

  • Van Slogteren GMS, Hoge JHC, Hooykaas PJJ, Schilperoort RA (1983) Clonal analysis of heterogeneous crown gall tumor tissues induced by wild type and shooter mutant strains of Agrobacterium tumefaciens - expression of T-DNA genes. Plant Mol Biol 2: 321–333

    Google Scholar 

  • Velten J, Willmitzer L, Leemans J, Ellis J, Deblaere R, Van Montagu M, Schell J (1983) TR genes involved in agropine production. In: Pühler A (ed) Molecular genetics of the bacteria-plant interaction. Springer, Berlin Heidelberg New York, pp 292–302

    Google Scholar 

  • Walden RM, Howell SH (1982) Intergenomic recombination events among pairs of defective cauliflower mosaic virus genomes in plants. J Mol Appl Genet 1: 447–456

    PubMed  CAS  Google Scholar 

  • Walden RM, Howell SH (1983) Uncut recombinant plasmids becoming nested cauliflower mo-saic virus genome infect plants by intragenomic recombination. Plant Mol Biol 2: 27–31

    CAS  Google Scholar 

  • Watson B, Currier TC, Gordon MP, Chilton M-D, Nester EW (1975) Plasmid required for vir-ulence of Agrobacterium tumefaciens. J Bacteriol 123: 255–264

    PubMed  CAS  Google Scholar 

  • Weiler EW, Spanier K (1981) Phytohormones in the formation of crown gall tumors. Planta (Berl) 153: 326–337

    CAS  Google Scholar 

  • White FF, Nester EW (1980 a) Hairy root: plasmid encodes virulence traits in Agrobacterium tumefaciens. J Bacteriol 144: 710–720

    Google Scholar 

  • White FF, Nester EW (1980 b) Relationship of plasmids responsible for hairy root and crown gall tumorigenicity. J Bacteriol 144: 710–720

    Google Scholar 

  • White FF, Ghidossi G, Gordon MP, Nester EW (1982) Tumor induction by Agrobacterium rhizogenes involves the transfer of plasmid DNA to the plant genome. Proc Natl Acad Sci USA 79: 3193–3197

    PubMed  CAS  Google Scholar 

  • Willmitzer L, De Beuckleer M, Lemmers M, Van Montagu M, Schell J (1980) The Ti-plasmidderived T-DNA is present in the nucleus and absent from plastids of plant grown crown gall cells. Nature (Lond) 287: 359–361

    CAS  Google Scholar 

  • Willmitzer L, Otten L, Simons G, Schmalenbach W, Schröder J, Schröder G, Van Montagu M, De Vos G, Schell J (1981 a) Nuclear and polysomal transcripts of T-DNA in octopine crown gall suspension and callus cultures. Mol Gen Genet 182: 255–262

    Google Scholar 

  • Willmitzer L, Schmalenbach W, Schell J (1981 b) Transcription of T-DNA in octopine and noplaine crown gall tumours is inhibited by low concentrations of s-amanitin. Nucleic Acids Res 9: 4801–4812

    Google Scholar 

  • Willmitzer L, Sanchez-Serrano J, Buschfeld E, Schell J (1982 a) DNA from Agrobacterium rhizogenes is transferred to and expressed in axenic hairy root plant tissues. Mol Gen Genet 186: 16–22

    Google Scholar 

  • Willmitzer L, Simons G, Schell J (1982 b) The TL-DNA in octopine crown gall tumors codes for seven well defined polyadenylated transcripts. EMBO J 1: 139–146

    Google Scholar 

  • Willmitzer L, Dhaese P, Schreier PH, Schmalenbach W, Van Montagu M, Schell J (1983) 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

    PubMed  CAS  Google Scholar 

  • Winter JA, Wright RL, Gurley WB (1984) Map locations of five transcripts homologous to TR DNA in tobacco and sunflower crown gall tumors. Nucleic Acids Res 12: 2391–2406

    PubMed  CAS  Google Scholar 

  • Woolston CJ, Covey SN, Penswick JR, Davies JW (1983) Aphid transmission and a polypeptide specified by a defined region of the cauliflower mosaic virus genome. Gene (Amst) 23: 1523

    Google Scholar 

  • Wöstemeyer A, Otten LABM, Schell J (1984) Sexual transmission of T-DNA in abnormal tobacco regenerants transformed by octopine and nopaline strains of Agrobacterium tumefaciens. Mol Gen Genet 194: 500–507

    Google Scholar 

  • Wullems GJ, Molendijk L, Ooms G, Schilperoort RA (1981 a) Differential expression of crown gall tumor markers in transformants obtained after in vitro Agrobacterium tumefaciens-induced transformation of cell wall regenerating protoplasts derived from Nicotiana tabacum. Proc Natl Acad Sci USA 78: 4344–4348

    Google Scholar 

  • Wullems GJ, Molendijk L, Ooms G, Schilperoort RA (1981 b) Retention of tumor markers in F1 progeny plants from in vitro induced octopine and nopaline tumor tissues. Cell 24:719727

    Google Scholar 

  • Wullems GJ, Krens FA, Schilperoort RA (1983) Plant protoplast transformation by Agrobacterium tumefaciens and its Ti-plasmid DNA. In: Pühler A (ed) Molecular genetics of the bacteria-plant interaction. Springer, Berlin Heidelberg New York, pp 274–283

    Google Scholar 

  • Xiong C, Muller S, Lebeurier G, Hirth L (1982) Identification by immunoprecipitation of cauliflower mosaic virus in vitro major translation product with a specific serum against viroplasm protein. EMBO J 1: 971–976

    PubMed  CAS  Google Scholar 

  • Yadav NS, Postle K, Saiki RK, Thomashow MF, Chilton M-D (1980) T-DNA of a crown gall teratoma is covalently joined to host plant DNA. Nature (Lond) 287: 458–461

    CAS  Google Scholar 

  • Yadav NS, Vanderleyden J, Bennett DR, Barnes WM, Chilton M-D (1982) Short direct repeats flank the T-DNA on a nopaline Ti-plasmid. Proc Natl Acad Sci USA 79: 6322–6326

    PubMed  CAS  Google Scholar 

  • Yamaoka N, Furusawa II, Yamamoto M (1982) Infection of turnip protoplast with cauliflower mosaic virus DNA. Virology 122: 503–505

    PubMed  CAS  Google Scholar 

  • Yang F, Simpson RB (1981) Revertant seedlings from crown gall tumors retain a portion of the bacterial Ti-plasmid DNA sequences. Proc Natl Acad Sci USA 78: 4151–4155

    PubMed  CAS  Google Scholar 

  • Yang F, Montoya AL, Merlo DJ, Drummond MH, Chilton MD, Nester EW, Gordon MP (1980) Foreign DNA sequences in crown gall teratomas and their fate during the loss of the tumorous traits. Mol Gen Genet 177: 707–714

    PubMed  CAS  Google Scholar 

  • Zambryski P, Holsters M, Krüger K, Depicker A, Schell J, Van Montagu M, Goodman HM (1980) Tumor DNA structure in plant cells transformed by A. tumefaciens. Science (Wash DC) 209: 1385–1391

    CAS  Google Scholar 

  • Zambryski P, Depicker A, Krüger K, Goodman HM (1982) Tumor induction by Agrobacterium tumefaciens: analysis of the boundaries of T-DNA. J Mol Appl Genet 1: 361–370

    PubMed  CAS  Google Scholar 

  • Zambryski P, Joos H, Genetello C, Leemans J, Van Montagu M, Schell J (1983) Ti-plasmid vector for the introduction of DNA into plant cells without alteration of their normal regeneration capacity. EMBO J 2: 2143–2150

    PubMed  CAS  Google Scholar 

  • Zambryski P, Herrera-Estrella L, De Block M, Van Montagu M, Schell J (1984, in press) The use of the Ti-plasmid of Agrobacterium to study the transfer and expression of foreign DNA in plant cells: new vectors and methods. In: Setlow J, Hollaender A (eds) Genetic engineering, principles and methods, vol 6. Plenum, New York

    Google Scholar 

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Yadav, N.S. (1986). Molecular Biology of Plant Cell Transformation. In: Reinert, J., Binding, H. (eds) Differentiation of Protoplasts and of Transformed Plant Cells. Results and Problems in Cell Differentiation, vol 12. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-540-39836-3_5

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