A chemical-inducible Cre-LoxP system allows for elimination of selection marker genes in transgenic apricot
文献类型: 外文期刊
第一作者: Petri, Cesar
作者: Petri, Cesar;Lopez-Noguera, Sonia;Wang, Hong;Garcia-Almodovar, Carlos;Alburquerque, Nuria;Burgos, Lorenzo;Wang, Hong
作者机构:
关键词: Fruit trees;Genetic engineering;Marker-free;Prunus armeniaca;Site-specific recombination;beta-Estradiol
期刊名称:PLANT CELL TISSUE AND ORGAN CULTURE ( 影响因子:2.711; 五年影响因子:2.73 )
ISSN:
年卷期:
页码:
收录情况: SCI
摘要: Transgenic plant development relies on the introduction of marker genes along with the gene(s) of interest to select and/or identify transgenic regenerants. Due to public concerns and regulatory issues, it would be advantageous to eliminate these marker genes once they are no longer needed. The chemical-inducible Cre-LoxP system is especially suitable for clonally-propagated plants, such as fruit trees, as no sexual crosses or rounds of transformation are required for marker-gene elimination. In this study, four transgenic pX6-GFP apricot (Prunus armeniaca L.) (cv. Helena) lines, carrying the gfp reporter gene encoding for the green fluorescent protein, were obtained following Agrobacterium tumefaciens-mediated transformation of leaf explants. The DNA site-specific recombination was precise and tightly controlled by the inducer beta-estradiol. Expression of the gfp gene was only detected when 3 mu M beta-estradiol was added to the medium. When nodal explants were incubated on a meristem development medium supplemented with 3 mu M beta-estradiol, marker gene elimination was observed in buds of all four transgenic lines, at an average frequency of 11.3 %, based on GFP expression. Further molecular analyses of four GFP-positive shoots, a single shoot from each transgenic line, revealed that DNA recombination was complete in two of shoots, but incomplete in the other two shoots.
分类号: Q942
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