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Agrobacterium-mediated transformation of the commercially important grapefruit cultivar Rio Red (Citrus paradisi Macf.)
Authors:Z N Yang  I L Ingelbrecht  E Louzada  M Skaria  T E Mirkov
Institution:(1) Department of Plant Pathology and Microbiology, The Texas A&M University Agricultural Experiment Station, 2415 E. Hwy 83, Weslaco, TX 78596, USA e-mail: e-mirkov@tamu.edu Fax: +1-956-9680641, US;(2) Citrus Center, The Texas A&M University – Kingsville, 312 N. Intl. Blvd., Weslaco, TX 78596, USA, US
Abstract: Transgenic plants of grapefruit cv. Rio Red (Citrus paradisi Macf.) have been obtained by Agrobacterium tumefaciens-mediated gene transfer using seedling-derived epicotyl segments as explants and kanamycin as the selective agent. The transformation procedure includes a shoot elongation phase with a liquid medium overlay, which provides additional selection against non-transgenic shoots. Transformed shoots are invigorated and multiplied on a non-selective medium prior to grafting, thus assuring that plants can be recovered from transgenic shoots. We have constructed a binary vector, pBin34SGUS, with an intron-containing β-glucuronidase gene (uidA) under the control of the Figwort mosaic virus 34S promoter. The 34S promoter efficiently drives uidA gene expression both in transient assays and in transgenic Rio Red leaf tissue, although at levels five- to sevenfold lower than the Cauliflower mosaic virus 35S promoter. An untranslatable coat protein gene (uncp) of the Citrus tristeza virus strain SY568 and the Galanthus nivalis agglutinin gene (gna) were inserted into pBin34SGUS and transgenic plants have been obtained. Stable integration of the uncp and gna genes was confirmed by Southern hybridization and gna gene expression was confirmed by Western blot analysis. Received: 2 February 2000 / Revision received: 21 June 2000 / Accepted: 29 June 2000
Keywords:Grapefruit  Agrobacterium tumefaciens  Genetic transformation  34S promoter  Galanthus nivalis agglutinin
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