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Agrobacterium mediated gene transformation of rice: Comparison of callus and shoot apex derived plants.

机译:农杆菌介导的水稻基因转化:愈伤组织和芽顶生植物的比较。

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Two serious drawbacks have limited the use of Agrobacterium in crop improvement: a host-range that appeared to exclude the cereals, and a practice of genotype-dependent plant regeneration from callus. Agrobacterium has recently been accepted for use in rice transformation; however, plant regeneration methods in use remain callus-based, and perpetuate many tissue culture problems. Regenerating plants from callus imposes specificity to regenerable genotypes and induces a wide range of permanent genetic mutations that are inherited by subsequent generations. Use of shoot apical meristems, in Agrobacterium-mediated transformations was proposed to overcome many of these problems since plant regeneration from shoots is simple and direct (Gould and Smith, 1988; Ulian et al., 1988; Gould and Smith, 1989). Use of shoot apex inoculations for Agrobacterium -mediated transformation of a cereal, corn (Zea mays L.), was immediately successful and permitted genotype-independent recovery of plants in 4–6 weeks (Gould et al., 1991). However, Hiei (1994) while proving that rice sustained genetic transformation by A. tumefaciens , also reported that inoculation of rice shoots failed to produce transgenic plants, and stated that shoot-based transformations were a fantasy. The objectives of this study, therefore, were to transform rice using Agrobacterium both shoot and callus-based approaches; and compare the transformation efficiencies, inheritance and somaclonal variation in the transgenic plants produced. Rice varieties Taipei309 and Texas rice cultivar Dixiebelle were transformed using A. tumefaciens LBA4404 (pTOK233) used by Hiei (1994), courtesy of Japan Tobacco. Transferred genes were detected in high molecular weight DNA of shoot derived plants up to three generations and callus derived plants up to two generations. A finding of this study was that homologous recombination occurred within the transferred T-DNA region after incorporation into plant DNA. Our conclusions are contrary to published reports, rice shoots were transformed by A. tumefaciens and by the LBA4404 (pTOK233) vector. The rate of transformation of shoots is similar to, but definitely not lower than, that of callus. Somaclonal variation appears in both shoot and callus-derived lines, but may be less severe in shoot-derived lines.
机译:两个严重的缺点限制了 Agrobacterium 在作物改良中的应用:宿主范围似乎排除了谷物,以及从愈伤组织中获得基因型依赖的植物。 农杆菌最近已被接受用于水稻转化。然而,使用中的植物再生方法仍然以愈伤组织为基础,并使许多组织培养问题永久存在。从愈伤组织再生植物对可再生基因型具有特异性,并诱导了后代继承的广泛的永久性遗传突变。有人提出在根癌农杆菌介导的转化中使用芽顶分生组织来克服许多这些问题,因为芽的植物再生是简单直接的(Gould and Smith,1988; Ulian et al。,1988; Gould和史密斯(1989)。利用芽尖接种进行农杆菌介导的谷物,玉米( Zea mays L。)的转化,该方法立即获得成功,并允许在4– 6周(Gould等,1991)。但是,Hiei(1994)在证明水稻通过 A进行遗传转化的同时。 tumefaciens ,还报道了接种水稻芽未能产生转基因植物,并指出基于芽的转化是一种幻想。因此,本研究的目的是使用基于芽和愈伤组织的农杆菌来转化水稻。并比较产生的转基因植物的转化效率,遗传和体细胞克隆变异。使用 A转化了水稻品种Taipei309和德克萨斯水稻品种Dixiebelle。 Hiei(1994)使用的tumefaciens LBA4404(pTOK233),由日本烟草提供。在高达三代的芽衍生植物和高达两代的愈伤组织衍生植物的高分子量DNA中检测到转移的基因。该研究的发现是在掺入植物DNA中后在转移的T-DNA区域内发生了同源重组。我们的结论与已发表的报道相反,水稻芽由 A转化。 tumefaciens 和LBA4404(pTOK233)载体。芽的转化率与愈伤组织相似,但绝对不低于愈伤组织。在茎和愈伤组织来源的品系中均出现体细胞克隆变异,但在茎衍生来源的品系中则可能不那么严重。

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