Pérez Hernández Juan B, Remy Serge, Swennen Rony, Sági László
Departamento de Fruticultura Tropical, Instituto Canario de Investigaciones Agrarias, Apartado 60, 38200 La Laguna, Santa Cruz de Tenerife, Spain.
Methods Mol Biol. 2006;344:167-75. doi: 10.1385/1-59745-131-2:167.
Cultivated bananas are vegetatively propagating herbs, which are difficult to breed because of widespread male and female sterility. As a complementary gene transfer method in banana, the described Agrobacterium protocol relies on highly regenerable embryogenic cell cultures. Embryogenic cells are infected and co-cultivated in the presence of acetosyringone with Agrobacterium tumefaciens harboring a binary plasmid vector to obtain a mixed population of transformed and untransformed plant cells. Transformed plant cells are promoted to grow for 2 to 3 mo on a cell colony induction medium containing the antibiotics geneticin or hygromycin as selective agents, while agrobacteria are counterselected by timentin. The whole procedure, including plant regeneration, takes approx 6 mo and results in an average frequency of 25 to 50 independent transgenic plants per plate, which equals 50 mg of embryogenic cells. This method has been applied to a wide range of cultivars and to generate large populations of transgenic colonies and plants for tagging genes and promoters in banana.
人工栽培的香蕉是通过营养繁殖的草本植物,由于普遍存在的雄性和雌性不育现象,其育种难度较大。作为香蕉中一种互补的基因转移方法,所述的农杆菌方案依赖于高度可再生的胚性细胞培养物。胚性细胞在乙酰丁香酮存在的情况下与携带二元质粒载体的根癌农杆菌一起感染并共培养,以获得转化和未转化植物细胞的混合群体。转化后的植物细胞在含有抗生素遗传霉素或潮霉素作为选择剂的细胞集落诱导培养基上促进生长2至3个月,而农杆菌则通过替卡西林进行反选择。整个过程,包括植物再生,大约需要6个月,平均每平板产生25至50株独立的转基因植株,这相当于50毫克胚性细胞。该方法已应用于广泛的品种,并用于产生大量的转基因菌落和植株,用于香蕉中基因和启动子的标记。