...
首页> 外文期刊>In Vitro Cellular and Development Biology. Plant: Journal of the Tissue Culture Association >Comparison of three selectable marker genes for transformation of tall fescue (Festuca arundinacea Schreb.) plants by particle bombardment
【24h】

Comparison of three selectable marker genes for transformation of tall fescue (Festuca arundinacea Schreb.) plants by particle bombardment

机译:通过粒子轰击法转化高羊茅(Festuca arundinacea Schreb。)植物的三种选择标记基因的比较

获取原文
获取原文并翻译 | 示例

摘要

A variety of selection systems have been developed for transformation of forage crops. To compare the most frequently used systems, we tested three selectable marker genes for their selection efficiency under four selection procedures for the production of transgenic tall fescue. Embryogenic calluses initiated from mature embryos were bombarded with three constructs containing either the phosphinothricin acetyltransferase (bar) gene, the hygromycin phosphotransferase (hpt) gene or the neomycin phosphotransferase II (nptII) gene. Transformation efficiency was strongly influenced by the selectable marker gene, selection procedure and genotype. The highest transformation efficiency was observed using the bar gene in combination with bialaphos. Average transformation efficiencies with bialaphos, phosphinothricin (glufosinate), hygromycin and paromomycin selection across the two callus lines used in the experiments were 9.4%, 4.4%, 5.2% and 1.6%, respectively. Southern blot analysis revealed the independent nature of the tested transgenic plants and a complex transgene integration pattern with multiple insertions.
机译:已经开发出多种选择系统用于饲料作物的转化。为了比较最常用的系统,我们在生产转基因羊茅的四种选择程序中测试了三种选择标记基因的选择效率。用含有膦丝菌素乙酰转移酶(bar)基因,潮霉素磷酸转移酶(hpt)基因或新霉素磷酸转移酶II(nptII)基因的三种构建物轰击成熟胚开始的胚性愈伤组织。选择性标记基因,选择步骤和基因型强烈影响转化效率。使用bar基因与bialaphos组合观察到最高的转化效率。在实验中使用的两个愈伤组织中,选择双丙氨磷,草丁膦(草铵膦),潮霉素和巴龙霉素的平均转化效率分别为9.4%,4.4%,5.2%和1.6%。 Southern印迹分析揭示了所测试的转基因植物的独立性质以及具有多个插入的复杂的转基因整合模式。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号