Department of Biochemistry and Microbiology, Centre for Forest Biology, University of Victoria, Victoria, BC, V8W 3P6, Canada.
Plant Cell Rep. 2010 Mar;29(3):211-21. doi: 10.1007/s00299-009-0806-z. Epub 2010 Jan 20.
Many economically important species of Populus, especially those in sections Aigeiros and Tacamahaca, remain recalcitrant to genetic transformation. In this study, a simple and reliable protocol was developed for the efficient Agrobacterium-mediated transformation of a difficult-to-transform, but commercially viable, hybrid poplar Populus nigra L. x P. maximowiczii A. Henry (NM6). A plant transformation vector designed to express the beta-glucuronidase (GUS) gene was used to detect transformation events at early stages of plant regeneration and to optimize parameters affecting poplar transformation. The use of zeatin riboside in shoot-induction medium, regeneration of shoots via indirect organogenesis, and early selection pressure were the major modifications that drastically improved the efficiency of poplar transformation and minimized the number of untransformed regenerants. Transgenic shoots were routinely obtained 4-10 weeks after co-culture with A. tumefaciens, with a greater than 90% rate of plant recovery. Stable transgene integration, ranging from a single insertion to ten copies per genome, was confirmed by Southern blot analysis. The mean transformation frequency was 36.3% and about two-thirds of the lines had 1-2 transgene copies. Among the explants, petioles and leaves had a higher transformation frequency than did stem segments. Growth characteristics and the morphology of transgenic poplar plants were identical to untransformed controls. These findings will accelerate the development of P. nigra x P. maximowiczii plants with novel traits, and may also be useful to improve transformation procedures for other Populus species.
许多经济上重要的杨属物种,特别是 Aigeiros 和 Tacamahaca 两个组的物种,对遗传转化仍然具有抗性。本研究开发了一种简单可靠的方法,用于高效地进行难以转化但具有商业可行性的杂种杨树 Populus nigra L. x P. maximowiczii A. Henry(NM6)的根癌农杆菌介导转化。设计用于表达β-葡萄糖醛酸酶(GUS)基因的植物转化载体用于在植物再生的早期阶段检测转化事件,并优化影响杨树转化的参数。在芽诱导培养基中使用玉米素核苷、通过间接器官发生再生芽以及早期选择压力是显著提高杨树转化效率并最大限度减少未转化再生体数量的主要改进措施。与根癌农杆菌共培养 4-10 周后,常规获得转基因芽,植物再生率大于 90%。通过 Southern blot 分析证实了稳定的转基因整合,从单个插入到每个基因组的 10 个拷贝不等。平均转化频率为 36.3%,约三分之二的系具有 1-2 个转基因拷贝。在外植体中,叶柄和叶片的转化频率高于茎段。转基因杨树植物的生长特性和形态与未转化对照相同。这些发现将加速具有新特性的 P. nigra x P. maximowiczii 植物的开发,也可能有助于改进其他杨属物种的转化程序。