Ishizaki Takuma, Kumashiro Takashi
Biological Resources Division, Japan International Research Center for Agricultural Sciences, 1-1 Ohwashi, Tsukuba, Ibaraki 305-8686, Japan.
Plant Cell Rep. 2008 Feb;27(2):319-27. doi: 10.1007/s00299-007-0465-x. Epub 2007 Oct 13.
We developed an efficient gene transfer method mediated by Agrobacterium tumefaciens for introgression of new rice for Africa (NERICA) cultivars, which are derivatives of interspecific hybrids between Oryza glaberrima Steud. and O. sativa L. Freshly isolated immature embryos were inoculated with A. tumefaciens LBA4404 that harbored binary vector pBIG-ubi::GUS or pIG121Hm, which each carried a hygromycin-resistance gene and a GUS gene. Growth medium supplemented with 500 mg/l cefotaxime and 20 mg/l hygromycin was suitable for elimination of bacteria and selection of transformed cells. Shoots regenerated from the selected cells on MS medium containing 20 g/l sucrose, 30 g/l sorbitol, 2 g/l casamino acids, 0.25 mg/l naphthaleneacetic acid, 2.5 mg/l kinetin, 250 mg/l cefotaxime, and 20 mg/l hygromycin. The shoots developed roots on hormone-free MS medium containing 30 mg/l hygromycin. Integration and expression of the transgenes were confirmed by PCR, Southern blot analysis, and histochemical GUS assay. Stable integration, expression, inheritance, and segregation of the transgenes were demonstrated by molecular and genetic analyses in the T(0) and T(1) generations. Most plants were normal in morphology and fertile. The transformation protocol produced stable transformants from 16 NERICA cultivars. We also obtained transformed plants by inoculation of calluses derived from mature seeds, but the frequency of transformation was lower and sterility was more frequent.
我们开发了一种由根癌农杆菌介导的高效基因转移方法,用于非洲新稻(NERICA)品种的基因渗入,NERICA品种是光稃稻(Oryza glaberrima Steud.)和栽培稻(O. sativa L.)种间杂种的衍生物。将刚分离的未成熟胚接种到携带二元载体pBIG-ubi::GUS或pIG121Hm的根癌农杆菌LBA4404中,每个载体都携带一个潮霉素抗性基因和一个GUS基因。添加500 mg/l头孢噻肟和20 mg/l潮霉素的生长培养基适合于除菌和转化细胞的筛选。从含有20 g/l蔗糖、30 g/l山梨醇、2 g/l酪蛋白氨基酸、0.25 mg/l萘乙酸、2.5 mg/l激动素、250 mg/l头孢噻肟和20 mg/l潮霉素的MS培养基上筛选出的细胞再生出芽。芽在含有30 mg/l潮霉素的无激素MS培养基上生根。通过PCR、Southern杂交分析和组织化学GUS检测证实了转基因的整合和表达。通过T(0)和T(1)代的分子和遗传分析证明了转基因的稳定整合、表达、遗传和分离。大多数植株形态正常且可育。该转化方案从16个NERICA品种中产生了稳定的转化体。我们还通过接种成熟种子衍生的愈伤组织获得了转化植株,但转化频率较低且不育现象更为常见。