Suppr超能文献

[Ac/Ds转座子系统在培育无标记基因转基因水稻中的应用]

[Application of Ac/Ds transposon system to genetate marker gene free transgenic plants in rice].

作者信息

Jin Wei-Zheng, Duan Rui-Jun, Zhang Fan, Chen Shuang-Yan, Wu Yun-Rong, Wu Ping

机构信息

State Key Laboratory of Plant Physiology and Biochemistry, College of Life Sciences, Zhejiang University, Hanrgzhou 310029, China.

出版信息

Sheng Wu Gong Cheng Xue Bao. 2003 Nov;19(6):668-73.

Abstract

It is critical to generate marker gene free transgenic plants for retransformating or eliminating the potential harmfulness of marker gene and its product. In this study, Ac/Ds transposon system was developed for removal of hpt selection marker gene to obtain marker-free transgenic plants in rice ( Oryza sativa L.). Ds element containing the interesting gene bar was constructed next to the selection marker gene hpt to get Ds-T-DNA. Rice plants were transformed by Agrobacterium tumefaciens EHA105 containing Ac-T-DNA and Ds-T-DNA respectively. Rice plant containing single copy Ac-T-DNA was crossed with plant containing single copy Ds-T-DNA to obtain the F1 plant containing both Ac and Ds elements. F1 plant was self-crossed to produce F2 progeny in which T-DNA insert and transposed Ds element segregated independently. Two plants contained Ds element but no hpt marker gene in total 100 F2 plants. The result indicated that Ac/Ds transposon system could be used as a vector system for generating marker gene free transgenic plants in rice.

摘要

为了进行重新转化或消除标记基因及其产物的潜在危害,培育无标记基因的转基因植物至关重要。在本研究中,开发了Ac/Ds转座子系统用于去除潮霉素磷酸转移酶(hpt)选择标记基因,以获得水稻(Oryza sativa L.)无标记转基因植物。在选择标记基因hpt旁边构建含有目的基因bar的Ds元件,得到Ds-T-DNA。分别用含有Ac-T-DNA和Ds-T-DNA的根癌农杆菌EHA105转化水稻植株。将含有单拷贝Ac-T-DNA的水稻植株与含有单拷贝Ds-T-DNA的植株杂交,获得同时含有Ac和Ds元件的F1植株。F1植株自交产生F2后代,其中T-DNA插入片段和转座的Ds元件独立分离。在总共100株F2植株中,有两株含有Ds元件但无hpt标记基因。结果表明,Ac/Ds转座子系统可作为一种载体系统用于培育水稻无标记转基因植物。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验