Abstract
A system for the production of transgenic plants was developed for the Oriental hybrid lily, Lilium cv. Acapulco, by Agrobacterium-mediated genetic transformation. Filament-derived calli were co-cultivated with A. tumefaciens strain EHA101/pIG121Hm, which harbored a binary vector carrying the neomycin phosphotransferase II, hygromycin phosphotransferase, and intron-containing β-glucuronidase genes in the T-DNA region. Six hygromycin-resistant (Hygr) culture lines were obtained from 200 calli by scratching them with sandpaper prior to inoculation and using NH4NO3-free medium for co-cultivation and a hygromycin-containing regeneration medium for selection. Hygr culture lines regenerated shoots, which developed into plantlets following transfer to a plant growth regulator-free medium. All of these plantlets were verified to be transgenic by GUS histochemical assay and inverse PCR analysis.
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Abbreviations
- AS :
-
Acetosyringone (3,5-dimethoxy-4-hydroxy-acetophenone)
- BA :
-
Benzyladenine
- CaMV :
-
Cauliflower mosaic virus
- GUS :
-
β-Glucuronidase
- HPT :
-
Hygromycin phosphotransferase
- Hyg r :
-
Hygromycin-resistant
- NOS :
-
Nopaline synthase
- NPTII :
-
Neomycin phosphotransferase II
- PGR :
-
Plant growth regulator
- PIC :
-
Picloram (4-amino-3,5,6-trichloropicolinic acid)
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Hoshi, Y., Kondo, M., Mori, S. et al. Production of transgenic lily plants by Agrobacterium-mediated transformation. Plant Cell Rep 22, 359–364 (2004). https://doi.org/10.1007/s00299-003-0700-z
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DOI: https://doi.org/10.1007/s00299-003-0700-z