uidA gene transfer and expression in maize microspores using the biolistic method |
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Authors: | M. F. Jardinaud A. Souvré G. Alibert M. Beckert |
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Affiliation: | (1) Laboratoire de Biotechnologie et Amélioration des Plantes, INP-ENSAT, 145 Avenue de Muret, F-31076 Toulouse Cedex, France;(2) INRA Station d'Amélioration des Plantes de Clermont-Ferrand, Clermont-Ferrand |
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Abstract: | Summary The ability to recover male gametophyte derived plants, which is necessary to get transformed haploid plants, was verified for a hybrid of maize. Using the isolated microspore culture technique, a 9 × 10–5 plant regeneration frequency was obtained. Maize microspores were bombarded with tungsten particles using a PDS He/1000 apparatus. GUS expression in the microspores was maximum with 1.1 m diameter tungsten microprojectiles for 1100 and 1350 psi helium pressures at a 6 cm distance between the launch point and the target cells. Increasing the amount of DNA coated on the microparticles from 1.66 to 4 g DNA/mg of particles allowed a two-fold and four-fold increase of the GUS-expressing microspore frequency for 1100 and 1350 psi helium pressure bombardment, respectively. Optimal concentration of solidifying agent in the bombardment support culture medium was found to be 1%. Cell density ranging from 25000 microspores/bombardment to 100000 microspores/bombardment did not affect the frequency of GUS-expressing microspores. Using these optimal conditions, the maximum frequency of GUS-expressing microspores was found to be about 9 × 10–4, while maintaining an embryo formation frequency about 5 × 10–4.Abbreviations GUS -glucuronidase - PEG polyethylene glycol |
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Keywords: | Biolistics Microspores GUS-expression Zea mays |
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