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Bioloistic-mediated Transformation of Cotton (Gossypium hirsutum L.): Embryogenic Calli as Explant  

Haq Ikram-ul (Plant Biotechnology Division, National Institute for Biotechnology and Genetic Engineering (NIBGE))
Asad Shaheen (Plant Biotechnology Division, National Institute for Biotechnology and Genetic Engineering (NIBGE))
Zafar Yusuf (Plant Biotechnology Division, National Institute for Biotechnology and Genetic Engineering (NIBGE))
Publication Information
Journal of Plant Biotechnology / v.7, no.4, 2005 , pp. 211-218 More about this Journal
Abstract
Genetic transformation was carried out by using biolistic gun method. The hypocotyl derived embryogenic calli (explants) of cotton (Gossypium hirsutum L.) cv. Cocker-312 were transformed with a recombinant pGreen II plasmid, in which both, bar (selection marker) and GUS (${\beta}$-glucuronidase) reporter genes were incorporated. Explants were arranged on osmoticum-containing medium (0.5M mannitol) 4 hours prior to and 16 hours after bombardment that was resulted into an increase about >80% for GUS stable expression. 3 days after bombardment, GUS assay was performed, which exhibited, $18.36{\pm}1.00$ calli showed blue spots. The transformed embryogenic calli were cultured on selection medium (@ 6 mg/L basta) for 3 months. The putative transgenic plants were developed via selective somatic embryogenesis (@1.50 mg/L basta); maximum $27.58{\pm}1.25$ somatic embryos were obtained while $17.47{\pm}1.00$ embryos developed into plantlets (@ 0.75mg/L basta). In five independent experiments, up to 7.24% transformation efficiency was recorded. The presence of the transgenes was analyzed by using PCR and southern hybridization analysis. The transgenic plants were developed with in 6-7 months, but mostly transformants were abnormal in morphology.
Keywords
biolistic transformation; cotton (Gossypium hirsutum L.); bialaphos; GUS; expression; embryogenic calli; somatic embryogenesis; transgene expression;
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