Abstract
A streamlined mini binary vector was constructed that is less than 1/2 the size of the pBIN19 backbone (3.5 kb). This was accomplished by eliminating over 5 kb of non-T-DNA sequences from the pBIN19 vector. The vector still retains all the essential elements required for a binary vector. These include a RK2 replication origin, the nptIII gene conferring kanamycin resistance in bacteria, both the right and left T-DNA borders, and a multiple cloning site (MCS) in between the T-DNA borders to facilitate cloning. Due to the reduced size, more unique restriction sites are available in the MCS, thus allowing more versatile cloning. Since the traF region was not included, it is not possible to mobilize this binary vector into Agrobacterium by triparental mating. This problem can be easily resolved by direct transformation. The mini binary vector has been demonstrated to successfully transform Arabidopsis plants. Based on this mini binary vector, a series of binary vectors were constructed for plant transformation.
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References
An, G., Watson, B., Stachel, S., Gordon, M.P. and Nester, E.W. 1985. New cloning vehicles for transformation of higher plants. EMBO J. 4: 277–284.
An, G. 1986. Development of plant promoter expression vectors and their use for analysis of different activity of nopaline synthase promoter in transformed tobacco tissue. Plant Physiol 81: 86–91.
Bechtold, N., Ellis, J. and Pelletier, G. 1993. In planta Agrobacterium-mediated gene transfer by infiltration of adult Arabidopsis thaliana plants. C.R. Acad. Sci. Paris, Life Sci. 316: 1194–1199.
Becker, D., Kemper, E., Schell, J. and Masterson, R. 1992. New plant binary vectors with selectable markers located proximal to the left T-DNA border. Plant Mol. Biol. 20: 1195–1197.
Bent, A.F. and Clough, S.J. 1998. Agrobacterium germ-line transformation: transformation of Arabidopsis without tissue culture. In: S.B. Gelvin and R.A. Schilperoort (Eds.), PlantMolecular Biology Manual, 2nd ed. Kluwer Academic Publishers, Dordrecht, Netherlands, pp. B7: 1–14.
Bevan, M. 1984. Binary Agrobacterium vector for plant transformation. Nucl. Acids Res. 12: 8711–8721.
Boutry, M., Nagy, F., Poulsen, C., Aoyagi, K. and Chua, N.-H. 1987. Targeting of bacterial chloramphenicol acetyltransferase to mitochondria in transgenic plants. Nature 328: 340–342.
Cangelosi, G.A., Best, E.A., Martinetti, G. and Nester, E.W. 1991. Genetic analysis of Agrobacterium. Meth. Enzymol. 204: 384–397.
Christensen, A.J. and Quail, P.H. 1996. Ubiquitin promoter-based vectors for high level expression of selectable and/or screenable marker genes in monocotyledonous plants. Transgen. Res. 5: 213–218.
Frisch, D.A., Harris-Haller, L.W., Yokubaitis, N.T., Thomas, T.L., Hardin, S.H. and Hall, T.C. 1995. Complete sequence of the binary vector Bin 19. Plant Mol. Biol. 27: 405–409.
Gleave, A.P. 1992. A versatile binary vector system with a TDNA organisational structure conducive to efficient integration of cloned DNA into the plant genome. PlantMol. Biol. 20: 1203–1207.
Guerineau, F., Woolston, S., Brooks, L. and Mullineaux, P. 1988. An expression cassette for targeting foreign proteins into chloroplasts. Nucl. Acids Res. 16: 11380–11388.
Hajdukiewicz, P., Svab, P.Z. and Maliga, P. 1994. The pBZP family of Agrobacterium binary vectors. Plant Mol. Biol. 25: 989–994.
Haseloff, J., Siemering, K.R., Prasher, D.C. and Hodge, S. 1997. Removal of a cryptic intron and subcellular localization of green fluorescent protein are required to mark transgenic Arabidopsis plants brightly. Proc. Natl. Acad. Sci USA 94: 2122–2127.
Hoekema, A., Hirsch, P.R., Hooykaas, P.J.J. and Schilperoort, R.A. 1983. A binary plant vector strategy based on separation of vir-and T-regions of the Agrobacterium tumefaciens Ti plasmid. Nature 303: 179–180.
Holsters, M., deWaele, D., Depecker, A.D., Messens, E., VanMontagu, M. and Schell, J. 1987. Transfection and transformation of A. tumefaciens. Mol. Gen. Genet. 163: 181–187.
Kempin, S.A., Liljegren, S.J., Block L.M., Rounsley, S.D., Yanofsky, M.F. and Lam, E. 1997. Targeted disruption in Arabidopsis. Nature 389: 802–803.
Klee, H.J., Yanofsky, M.F. and Nester, E.W. 1985. Vectors for transformation of higher plants. Bio/technology 3: 637–642.
Ma, H., Yanofsky, M.F., Klee, H.J., Bowman, J.L. and Meyerowitz, E.M. 1992. Vectors for plant transformation and cosmid libraries. Gene 117: 161–167.
Miao, Z.-H. and Lam, E. 1995. Targeted disruption of the TGA3 locus in Arabidopsis thaliana. Plant J. 7: 359–365.
Sambrook, J., Fritsch, E.F. and Maniatis, T. 1989. Molecular Cloning: A Laboratory Manual, 2nd ed., Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY (1989).
Schardl, C.L., Byrd, A.D., Benzion, G., Altschuler, M.A., Hildebrand, D.F. and Hunt, A.G. 1987. Design and construction of a versatile system for the expression of foreign genes in plants. Gene 61: 1–11.
Simoens, C., Alliotte, T., Mendel, R., Müller, A., Schiemann, J., Van Lijsebettens, M., Schell, J., Van Montagu, M. and Inzé, D. 1986. A binary vector for transferring genomic libraries to plants. Nucl. Acids Res. 14: 8073–8090.
Wang, K., Herrera-Estrella, L., Van Montagu, M. and Zambryski, P. 1984. Right 25 bp terminus sequence of the nopaline T-DNA is essential for and determines direction of DNA transfer from Agrobacterium to the plant genome. Cell 38: 455–462.
Xiang, C., Miao, Z. and Lam, E. 1997. DNA-binding properties, genomic organization and expression pattern of TGA6, a new member of the TGA family of bZIP transcription factors in Arabidopsis thaliana. Plant Mol. Biol. 34: 403–415.
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Xiang, C., Han, P., Lutziger, I. et al. A mini binary vector series for plant transformation. Plant Mol Biol 40, 711–717 (1999). https://doi.org/10.1023/A:1006201910593
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DOI: https://doi.org/10.1023/A:1006201910593