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通过农杆菌介导转化产生无标记和/或无骨干的转基因小麦植株。

Generation of Marker- and/or Backbone-Free Transgenic Wheat Plants via -Mediated Transformation.

作者信息

Wang Gen-Ping, Yu Xiu-Dao, Sun Yong-Wei, Jones Huw D, Xia Lan-Qin

机构信息

Department of Plant Gene Resources and Molecular Design, Institute of Crop Sciences, Chinese Academy of Agricultural Sciences (CAAS)Beijing, China; Cereal Crops Research Laboratory of Hebei Province, National Millet Improvement Center, Institute of Millet Crops, Hebei Academy of Agriculture and Forestry SciencesShijiazhuang, China.

Department of Plant Gene Resources and Molecular Design, Institute of Crop Sciences, Chinese Academy of Agricultural Sciences (CAAS) Beijing, China.

出版信息

Front Plant Sci. 2016 Sep 21;7:1324. doi: 10.3389/fpls.2016.01324. eCollection 2016.

Abstract

Horizontal transfer of antibiotic resistance genes to animals and vertical transfer of herbicide resistance genes to the weedy relatives are perceived as major biosafety concerns in genetically modified (GM) crops. In this study, five novel vectors which used and as a reporter gene and a selection marker gene, respectively, were constructed based on the pCLEAN dual binary vector system. Among these vectors, 1G7B and 5G7B carried two T-DNAs located on two respective plasmids with 5G7B possessing an additional gene. 5LBTG154 and 5TGTB154 carried two T-DNAs in the target plasmid with either one or double right borders, and 5BTG154 carried the selectable marker gene on the backbone outside of the T-DNA left border in the target plasmid. In addition, 5BTG154, 5LBTG154, and 5TGTB154 used pAL154 as a helper plasmid which contains Komari fragment to facilitate transformation. These five dual binary vector combinations were transformed into strain AGL1 and used to transform durum wheat cv Stewart 63. Evaluation of the co-transformation efficiencies, the frequencies of marker-free transgenic plants, and integration of backbone sequences in the obtained transgenic lines indicated that two vectors (5G7B and 5TGTB154) were more efficient in generating marker-free transgenic wheat plants with no or minimal integration of backbone sequences in the wheat genome. The vector series developed in this study for generation of marker- and/or backbone-free transgenic wheat plants -mediated transformation will be useful to facilitate the creation of "clean" GM wheat containing only the foreign genes of agronomic importance.

摘要

抗生素抗性基因向动物的水平转移以及除草剂抗性基因向杂草近缘种的垂直转移被视为转基因作物的主要生物安全问题。在本研究中,基于pCLEAN双元载体系统构建了五个新型载体,分别使用[具体基因1]和[具体基因2]作为报告基因和选择标记基因。在这些载体中,1G7B和5G7B携带两个位于各自质粒上的T-DNA,其中5G7B还拥有一个额外的[具体基因3]。5LBTG154和5TGTB154在目标质粒中携带两个T-DNA,具有一个或两个右边界,而5BTG154在目标质粒的T-DNA左边界外侧的骨架上携带选择标记基因。此外,5BTG154、5LBTG154和5TGTB154使用pAL154作为辅助质粒,该质粒包含Komari片段以促进转化。将这五个双元载体组合转化到农杆菌AGL1菌株中,并用于转化硬粒小麦品种Stewart 63。对共转化效率、无标记转基因植株的频率以及所得转基因株系中骨架序列的整合情况进行评估表明,两个载体(5G7B和5TGTB154)在产生无标记转基因小麦植株方面更有效,且小麦基因组中骨架序列的整合没有或极少。本研究开发的用于通过[具体介导方式]转化产生无标记和/或无骨架转基因小麦植株的载体系列,将有助于创建仅包含具有农艺重要性的外源基因的“清洁”转基因小麦。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f38e/5030305/2fbce78086c7/fpls-07-01324-g0001.jpg

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