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首页> 外文期刊>Plant Cell, Tissue and Organ Culture: An International Journal on in Vitro Culture of Higher Plants >Establishment of embryogenic cell suspension cultures and Agrobacterium-mediated transformation in an important Cavendish banana cv. Robusta (AAA)
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Establishment of embryogenic cell suspension cultures and Agrobacterium-mediated transformation in an important Cavendish banana cv. Robusta (AAA)

机译:在重要的卡文迪许香蕉简历中建立胚性细胞悬浮培养物和农杆菌介导的转化。罗布斯塔(AAA)

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摘要

Establishment of an efficient protocol for regeneration and genetic transformation is required in banana for the incorporation of useful traits. Therefore an efficient method has been developed for somatic embryogenesis, plant regeneration and transformation of Cavendish banana cultivar Robusta (AAA). Embryogenic cell suspension culture (ECS) was established using immature male flowers. Percentage appearance of embryogenic callus and distinct globular embryos was 10.3 and 11.1, respectively. ECS obtained was cocultivated under different cocultivation conditions with Agrobacterium tumefaciens strain EHA105 harboring pCAMBIA 1301 plant expression vector. Up to 30 transgenic plants/50 mg settled cell volume (SCV) was obtained with cocultivation in semisolid medium whereas no transgenics could be obtained with parallel experiments carried out in liquid medium. Histochemical GUS assay in different tissues of putatively transformed plants demonstrated expression of uidA gene. Among the putatively transformed plants obtained, a set of 4 were confirmed by PCR analysis and stable integration of the transgene by Southern analysis. GUS specific activity measured by a MUG (4-methylumbelliferyl-beta-d-glucuronide) based flourometric assay revealed increase in transient GUS expression in semisolid as well as liquid cocultivation with centrifugation. This is the first report showing somatic embryogenesis and Agrobacterium tumefaciens mediated transformation using embryogenic cell suspension cultures in an important Cavendish banana cultivar Robusta. The present protocol will make possible agronomic improvement of this important commercially grown cultivar by introduction of disease resistance characteristics and antisense-mediated delayed fruit ripening strategies. Further, it will also assist in functional characterization of new gene or promoter elements isolated from this or other cultivars of banana.
机译:香蕉中需要建立有效的再生和遗传转化方案,以纳入有用的性状。因此,已经开发了一种有效的方法用于卡文迪许香蕉栽培品种罗布斯塔(AAA)的体细胞胚发生,植物再生和转化。使用未成熟的雄花建立胚性细胞悬浮培养物(ECS)。胚性愈伤组织和不同球状胚的外观百分比分别为10.3和11.1。将获得的ECS在不同的共培养条件下与带有pCAMBIA 1301植物表达载体的根癌农杆菌菌株EHA105共培养。在半固体培养基中共培养最多可获得30种转基因植物/ 50 mg沉降细胞体积(SCV),而在液体培养基中进行平行实验则无法获得转基因植物。组织化学GUS测定法在推定转化的植物的不同组织中证明了uidA基因的表达。在获得的推定转化的植物中,通过PCR分析确认了一组4个,并且通过Southern分析证实了转基因的稳定整合。通过基于MUG(4-甲基伞形酮-β-d-葡萄糖醛酸)的荧光测定法测量的GUS比活性揭示了半固体以及液体与离心共培养中瞬时GUS表达的增加。这是第一个报告,显示了在重要的卡文迪许香蕉品种罗布斯塔中使用胚性细胞悬浮培养物进行体细胞胚发生和根癌农杆菌介导的转化。通过引入抗病性特征和反义介导的延迟果实成熟策略,本方案将使这一重要的商业化栽培品种的农艺性改良成为可能。此外,它也将有助于从该香蕉或其他香蕉品种中分离的新基因或启动子元件的功能表征。

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