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Open Access Highly Accessed Research article

Genetic transformation of Vitis vinifera via organogenesis

Bruno Mezzetti1*, Tiziana Pandolfini2, Oriano Navacchi3 and Lucia Landi1

Author Affiliations

1 Dipartimento Biotecnologie Agrarie e Ambientali, University of Ancona, Via Brecce Bianche 60100 – Ancona Italy

2 Dipartimento Scientifico Tecnologico, University of Verona, Strada Le Grazie, 37134 Verona Italy

3 Vitroplant, Via Loreto – 47023 Cesena Italy

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BMC Biotechnology 2002, 2:18  doi:10.1186/1472-6750-2-18

Published: 27 September 2002

Abstract

Background

Efficient transformation and regeneration methods are a priority for successful application of genetic engineering to vegetative propagated plants such as grape. The current methods for the production of transgenic grape plants are based on Agrobacterium-mediated transformation followed by regeneration from embryogenic callus. However, grape embryogenic calli are laborious to establish and the phenotype of the regenerated plants can be altered.

Results

Transgenic grape plants (V. vinifera, table-grape cultivars Silcora and Thompson Seedless) were produced using a method based on regeneration via organogenesis. In vitro proliferating shoots were cultured in the presence of increasing concentrations of N6-benzyl adenine. The apical dome of the shoot was removed at each transplantation which, after three months, produced meristematic bulk tissue characterized by a strong capacity to differentiate adventitious shoots. Slices prepared from the meristematic bulk were used for Agrobacterium-mediated transformation of grape plants with the gene DefH9-iaaM. After rooting on kanamycin containing media and greenhouse acclimatization, transgenic plants were transferred to the field. At the end of the first year of field cultivation, DefH9-iaaM grape plants were phenotypically homogeneous and did not show any morphological alterations in vegetative growth. The expression of DefH9-iaaM gene was detected in transgenic flower buds of both cultivars.

Conclusions

The phenotypic homogeneity of the regenerated plants highlights the validity of this method for both propagation and genetic transformation of table grape cultivars. Expression of the DefH9-iaaM gene takes place in young flower buds of transgenic plants from both grape cultivars.

Keywords:
Vitis vinifera; meristem regeneration; genetic transformation; gene expression; DefH9-iaaM gene