Becker D K, Dugdale B, Smith M K, Harding R M, Dale J L
Centre for Molecular Biotechnology, School of Life Sciences, Queensland University of Technology, GPO Box 2434, Brisbane, Queensland 4001, Australia e-mail:
Maroochy Research Station, Queensland Horticulture Institute, Department of Primary Industries, Queensland, Australia, , , , , , AU.
Plant Cell Rep. 2000 Jan;19(3):229-234. doi: 10.1007/s002990050004.
An effective method has been developed for the stable transformation and regeneration of Cavendish banana (Musa spp. AAA group) cv 'Grand Nain' by microprojectile bombardment. Embryogenic cell suspensions were initiated using immature male flowers as the explant. Cells were co-bombarded with the neomycin phosphotransferase (nptII) selectable marker gene under the control of a banana bunchy top virus (BBTV) promoter or the CaMV 35S promoter, and either the β-glucuronidase (uidA) reporter gene or BBTV genes under the control of the maize polyubiquitin promoter. Plants were regenerated, under selection with kanamycin, that were co-transformed with nptII and either the uidA or BBTV genes. Molecular characterisation of transformants demonstrated that the transgenes had been stably integrated into the banana genome.
已经开发出一种通过微弹轰击实现卡文迪什香蕉(Musa spp. AAA组)品种‘大矮蕉’稳定转化和再生的有效方法。以未成熟雄花为外植体建立胚性细胞悬浮系。细胞与在香蕉束顶病毒(BBTV)启动子或CaMV 35S启动子控制下的新霉素磷酸转移酶(nptII)选择标记基因,以及在玉米多聚泛素启动子控制下的β-葡萄糖醛酸酶(uidA)报告基因或BBTV基因共同轰击。在卡那霉素选择下再生出与nptII以及uidA或BBTV基因共转化的植株。转化体的分子特征表明转基因已稳定整合到香蕉基因组中。