O'Kennedy M M, Burger J T, Botha F C
CSIR Food, Biological and Chemical Technologies, P.O. Box 395, 0001, Pretoria, South Africa.
Plant Cell Rep. 2004 Apr;22(9):684-90. doi: 10.1007/s00299-003-0746-y. Epub 2004 Jan 15.
Fertile transgenic pearl millet plants expressing a phosphomannose isomerase (PMI) transgene under control of the maize ubiquitin constitutive promoter were obtained using the transformation system described here. Proliferating immature zygotic embryos were used as target tissue for bombardment using a particle inflow gun. Different culture and selection strategies were assessed in order to obtain an optimised mannose selection protocol. Stable integration of the manA gene into the genome of pearl millet was confirmed by PCR and Southern blot analysis. Stable integration of the manA transgene into the genome of pearl millet was demonstrated in T1 and T2 progeny of two independent transformation events with no more than four to ten copies of the transgene. Similar to results obtained from previous studies with maize and wheat, the manA gene was shown to be a superior selectable marker gene for improving transformation efficiencies when compared to antibiotic or herbicide selectable marker genes.
利用本文所述的转化系统,获得了在玉米泛素组成型启动子控制下表达磷酸甘露糖异构酶(PMI)转基因的可育转基因珍珠粟植株。增殖的未成熟合子胚用作粒子流入枪轰击的靶组织。评估了不同的培养和选择策略,以获得优化的甘露糖选择方案。通过PCR和Southern印迹分析证实了manA基因稳定整合到珍珠粟基因组中。在两个独立转化事件的T1和T2后代中证明了manA转基因稳定整合到珍珠粟基因组中,转基因拷贝数不超过4至10个。与先前对玉米和小麦的研究结果相似,与抗生素或除草剂选择标记基因相比,manA基因被证明是提高转化效率的优良选择标记基因。