Horticulture and Crop Science Department, Ohio Agricultural Research and Development Center, The Ohio State University, 44691, Wooster, OH, USA.
Plant Cell Rep. 1996 Mar;15(7):500-5. doi: 10.1007/BF00232982.
Particle bombardment offers a simple method for the introduction of DNA into plant cells. Multiple DNA fragments may be introduced on a single plasmid or on separate plasmids (co-transformation). To investigate some of the properties and limits of co-transformation, 12 different plasmids were introduced into embryogenic suspension culture tissue of soybean [Glycine max (L.) Merrill] via particle bombardment. The DNAs used for co-transformation included 10 plasmids containing KFLP markers for maize and 2 plasmids separately encoding hygromycin-resistance and ß-glucuronidase. Two weeks following bombardment with the 12 different plasmids, suspension culture tissue was placed under hygromycin selection. Hygromycin-resistant clones were isolated after an additional 5 to 6 weeks. Southern hybridization analysis of 26 hygromycin-resistant embryogenic clones verified the presence of introduced plasmid DNAs. All of the co-transforming plasmids were present in most of the transgenic soybean clones and there was no preferential uptake and integration of any of the plasmids. The copy number of individual plasmids was approximately equal within clones but highly variable between clones. While some clones contained as few as zero to three copies of each plasmid, others clones contained as many as 10 to 15 copies of each of the 12 different plasmids.
粒子轰击为将 DNA 导入植物细胞提供了一种简单的方法。多个 DNA 片段可以在单个质粒或多个质粒(共转化)上导入。为了研究共转化的一些特性和限制,我们通过粒子轰击将 12 种不同的质粒导入大豆(Glycine max(L.)Merrill)的胚性悬浮培养组织中。用于共转化的 DNA 包括 10 个含有玉米 KFLP 标记的质粒和 2 个分别编码潮霉素抗性和β-葡萄糖醛酸酶的质粒。用 12 种不同的质粒轰击 2 周后,将悬浮培养组织置于潮霉素选择下。在另外 5 到 6 周后,分离出潮霉素抗性克隆。对 26 个潮霉素抗性胚性克隆的 Southern 杂交分析证实了引入的质粒 DNA 的存在。大多数转基因大豆克隆中都存在所有共转化的质粒,并且没有任何质粒的优先摄取和整合。单个质粒的拷贝数在克隆内大致相等,但在克隆间高度可变。虽然一些克隆每个质粒的拷贝数少至零到三个,而其他克隆每个质粒的拷贝数多达 10 到 15 个。