...
首页> 外文期刊>Molecular Plant-Microbe Interactions >Determination of the T-DNA Transfer and the T-DNA Integration Frequencies upon Cocultivation of Arabidopsis thaliana Root Explants
【24h】

Determination of the T-DNA Transfer and the T-DNA Integration Frequencies upon Cocultivation of Arabidopsis thaliana Root Explants

机译:拟南芥根外植体共培养时T-DNA转移和T-DNA整合频率的确定

获取原文
   

获取外文期刊封面封底 >>

       

摘要

Using the Cre/lox recombination system, we analyzed the extent to which T-DNA transfer to the plant cell and T-DNA integration into the plant genome determine the transformation and cotransformation frequencies of Arabidopsis root cells. Without selection for transformation competence, the stable transformation frequency of shoots obtained after cocultivation and regeneration on nonselective medium is below 0.5%. T-DNA transfer and expression occur in 5% of the shoots, indicating that the T-DNA integrates in less than 10% of the transiently expressing plant cells. A limited fraction of root cells, predominantly located at the wounded sites and in the pericycle, are competent for interaction with agrobacteria and the uptake of a T-DNA, as demonstrated by histochemical GUS staining. When selection for transformation competence is applied, the picture is completely different. Then, approximately 50% of the transformants show transient expression of a second, nonselected T-DNA and almost 50% of these cotransferred T-DNAs are integrated into the plant genome. Our results indicate that both T-DNA transfer and T-DNA integration limit the transformation and cotransformation frequencies and that plant cell competence for transformation is based on these two factors.
机译:使用Cre / lox重组系统,我们分析了T-DNA转移到植物细胞和T-DNA整合到植物基因组中的程度决定了拟南芥根细胞的转化和共转化频率。在没有选择转化能力的情况下,在非选择性培养基上共培养和再生后获得的芽的稳定转化频率低于0.5%。 T-DNA的转移和表达发生在5%的芽中,这表明T-DNA整合在少于10%的瞬时表达植物细胞中。正如组织化学GUS染色所证实的那样,有限比例的根细胞主要位于受伤部位和周周,能够与农杆菌相互作用并吸收T-DNA。当施加用于转化能力选择,画面是完全不同的。然后,大约50%的转化子显示出第二个非选择的T-DNA的瞬时表达,这些共转移的T-DNA的几乎50%被整合到植物基因组中。我们的结果表明,T-DNA转移和T-DNA整合都限制了转化和共转化的频率,而植物细胞的转化能力基于这两个因素。

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