RESUMEN
A genetic transformation procedure for Chamaecyparis obtusa was developed after co-cultivation of embryogenic tissues with disarmed Agrobacterium tumefaciens strain C58/pMP90, which harbours the sgfp (synthetic green fluorescent protein) visual reporter and nptII (neomycin phoshotransferase II) selectable marker genes. The highest transformation frequency was 22.5 independent transformed lines per dish (250 mg embryogenic tissue) following selection on kanamycin medium. Transgenic plantlets were regenerated through the maturation and germination of somatic embryos. The intensity of GFP fluorescence, observed under a fluorescence microscope, varied from very faint to relatively strong, depending on the transgenic line or part of the transgenic plant. The integration of the genes into the genome of regenerated plantlets was confirmed by Southern blot analysis.
Asunto(s)
Agrobacterium tumefaciens/genética , Chamaecyparis/genética , Plantas Modificadas Genéticamente/genética , Regeneración/genética , Semillas/genética , Transformación Genética/genética , Biomarcadores , Células Cultivadas , Chamaecyparis/embriología , Técnicas de Cocultivo , Regulación de la Expresión Génica de las Plantas/genética , Técnicas de Transferencia de Gen , Genes Reporteros , Vectores Genéticos/genética , Genoma de Planta , Proteínas Fluorescentes Verdes/genética , Kanamicina Quinasa/genética , Plantas Modificadas Genéticamente/embriología , Semillas/embriología , Transgenes/genéticaRESUMEN
We established a plant regeneration system for Hinoki cypress (Chamaecyparis obtusa) via somatic embryogenesis. Embryogenic tissues were successfully induced on three kinds of Smith media from megagametophyte explants containing pre-cotyledonary embryos of C. obtusa plus-trees. Factors affecting somatic embryo maturation were examined. The concentration of polyethylene glycol 4000 in the medium was a critical factor for embryo maturation and its effective concentration was 150 g/l. The addition of 30 g/l maltose to the medium had a positive effect on embryo maturation, but sucrose was ineffective. The mature somatic embryos germinated at a germination frequency of approximately 60%, and the presence of activated charcoal was effective in stimulating plantlet growth. The plantlets acclimatized successfully in a greenhouse. To our knowledge, this is first report describing details of a plant regeneration method for C. obtusa via somatic embryogenesis.
