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Agrobacterium-medmted genetic transformation of commercially elite rice restorer line using nptll gene as a plant selection marker

机译:农杆菌介导的以nptll基因为植物选择标记的优良水稻恢复系的遗传转化

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Transformation of commercially important indica cultivars remains challenging for the scientific community even though Agrobacterium-mediated transformation protocols for a few indica rice lines have been well established. We report successful transformation of a commercially important restorer line JK1044R of indica rice hybrid JKRH 401. While following existing protocol, we optimized several parameters for callusing, regeneration and genetic transformation of JK1044R. Calli generated from the ricescutellum tissue were used for transformation by Agrobacterium harboring pCAMBIA2201. A novel two tire selection scheme comprising of Geneticin (G418) and Paramomycin were deployed for selection of transgenic calli as well as regenerated plantlets that expressed neomycin phosphotransferase-^ gene encoded by the vector. One specific combination of G418 (30 mg F1) and Paramomycin (70 mg F1) was very effective for calliselection. Transformed and selected calli were detected by monitoring the expression of the reporter gene uidA (GUS). Regenerated plantlets were confirmed through PCR analysis of nptll and gus genes specific primers as well as dot blot using gus gene specific as probe.
机译:尽管已经建立了农杆菌介导的几种in稻品系的转化方案,但商业上重要的d稻品种的转化对科学界仍然具有挑战性。我们报告了rice稻杂交种JKRH 401的商业上重要的恢复系JK1044R的成功转化。在遵循现有协议的同时,我们优化了JK1044R的愈伤组织,再生和遗传转化的几个参数。从稻壳组织产生的愈伤组织被具有pCAMBIA2201的农杆菌用于转化。包括遗传霉素(G418)和帕拉霉素的新颖的两种轮胎选择方案被用于选择转基因愈伤组织以及表达由载体编码的新霉素磷酸转移酶β基因的再生小植株。 G418(30 mg F1)和Paramomycin(70 mg F1)的一种特定组合非常有效。通过监测报告基因uidA(GUS)的表达来检测转化和选择的愈伤组织。通过对nptII和gus基因特异引物的PCR分析以及以gus基因特异的探针进行斑点印迹,确认了再生的幼苗。

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