Department of Soil and Crop Sciences, Texas A&M University, College Station, Texas 77843.
Plant Physiol. 1991 Feb;95(2):426-34. doi: 10.1104/pp.95.2.426.
Agrobacterium tumefaciens is established as a vector for gene transfer in many dicotyledonous plants but is not accepted as a vector in monocotyledonous plants, especially in the important Gramineae. The use of Agrobacterium to transfer genes into monocot species could simplify the transformation and improvement of important crop plants. In this report we describe the use of Agrobacterium to transfer a gene into corn, the regeneration of plants, and detection of the transferred genes in the F(1) progeny. Shoot apices of Zea mays L. variety Funk's G90 were cocultivated with A. tumefaciens EHA 1, which harbored the plasmid pGUS3 containing genes for kanamycin resistance (NPT II) and beta-glucuronidase (GUS). Plants developed from these explants within 4 to 6 weeks. Fluorometric GUS assays of leaves and immature seeds from the plants exhibited low GUS activity. Both NOS and GUS gene fragments were amplified by polymerase chain reaction in the DNA isolated from the F(1) generations of one of the original transformed plants. Southern analysis showed both GUS and NPT probes hybridized to DNA in several of the F(1) progeny, demonstrating the incorporation of GUS and NPT II genes into high molecular weight DNA. These data establish successful gene transfer and sexual inheritance of the genes.
根癌农杆菌被确立为许多双子叶植物基因转移的载体,但不能作为单子叶植物,尤其是重要的禾本科植物的载体。利用根癌农杆菌将基因转移到单子叶植物物种中,可以简化重要作物的转化和改良。在本报告中,我们描述了利用根癌农杆菌将基因转移到玉米中,再生植株,并在 F1 后代中检测到转移的基因。玉米品种 Funk's G90 的茎尖与携带质粒 pGUS3 的根癌农杆菌 EHA1 共培养,该质粒包含卡那霉素抗性(NPT II)和β-葡萄糖醛酸酶(GUS)基因。这些外植体在 4 至 6 周内发育成植株。来自这些植株的叶片和未成熟种子的荧光 GUS 分析显示出低的 GUS 活性。NOS 和 GUS 基因片段都在来自一个原始转化植株的 F1 代的 DNA 中通过聚合酶链反应扩增。Southern 分析显示,GUS 和 NPT 探针都与 F1 后代中的几种 DNA 杂交,表明 GUS 和 NPT II 基因已整合到高分子量 DNA 中。这些数据确立了基因转移和基因的有性遗传的成功。