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首页> 外文期刊>In Vitro Cellular and Development Biology. Plant: Journal of the Tissue Culture Association >Rapid genotype 'independent' Zea mays L. (maize) transformation via direct somatic embryogenesis
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Rapid genotype 'independent' Zea mays L. (maize) transformation via direct somatic embryogenesis

机译:快速基因型“独立”Zea Mays L.(玉米)通过直接体细胞胚胎发生转化

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摘要

Constitutive expression of the Zea mays L. (maize) morphogenic transcription factors Baby Boom (Bbm) and Wuschel2 (Wus2) in maize can not only greatly increase transformation efficiency but can also induce phenotypic abnormalities and sterility. In an effort to alleviate the pleiotropic effects of constitutive expression, a genome wide search was undertaken to find suitable maize promoters to drive tissue and timing-specific expression of the transformation enhancing genes Bbm and Wus2. A promoter from a maize phospholipid transferase protein gene (Zm-PLTPpro) was identified based on its expression in leaves, embryos, and callus while being downregulated in roots, meristems, and reproductive tissues. When Zm-PLTPpro driving Bbm was transformed into immature maize embryos along with a Wus2 expression cassette driven by the nopaline synthase promoter (Nos(pro)::Wus2) abundant somatic embryos rapidly formed on the scutella. These embryos were individual and uniformly transformed and could be directly germinated into plants without a callus phase. Transformed plants could be sent to the greenhouse in as little as 1 mo and regenerated plants matched the seed-derived phenotype for the inbred and were fertile. However, T1 seed from these plants had poor germination. Replacing Nospro with a maize auxin-inducible promoter (Zm-Axig1(pro)) in combination with ZmPLTP(pro)::Bbm, allowed healthy, fertile plants to be regenerated. Single-copy T1 seed germinated normally and had a predominantly wild-type inbred phenotype. For maize, this callus-free transformation process has worked in all inbred lines tested.
机译:玉米Zea 5月L.(玉米)形态发生转录因子婴儿繁殖(BBM)和WUS3EL2(WUS2)的组成型表达不能极大地提高转化效率,但也可以诱导表型异常和无菌性。为了缓解本构表达的脂肪效应,进行了基因组广泛的搜索,以找到合适的玉米启动子以驱动组织和时序的转化增强基因BBM和WUS2的表达。玉米磷脂转移酶蛋白基因(ZM-PLTPPRO)的启动子于基于其在叶,胚胎和愈伤组织中的表达而鉴定,同时在根,分泌和生殖组织中下调。当ZM-PLTPPRO驱动BBM转化成未成熟的玉米胚胎以及由Nopaline合成酶启动子(NOS(Pro):: WUS2)驱动的WUS2表达盒(NOS(PRO):: WUS2)迅速形成在Scutella迅速形成的体细胞胚胎。这些胚胎是个体的并且均匀转化,并且可以直接发芽到没有愈伤组织的植物中。转化的植物可以送到温室,只需1个Mo和再生植物就匹配了种子衍生的表型为近交并且是肥沃的。然而,来自这些植物的T1种子萌发差。用玉米植物蛋白诱导型启动子(ZM-AXIG1(PRO))与ZMPLTP(PRO):: BBM组合替代NoSPro,允许再生,肥沃的植物进行健康,肥沃的植物。单拷贝T1种子通常发芽,并且主要具有野生型近亲表型。对于玉米,这种无愈伤贺卡的转换过程已经在所有测试的近交线中工作。

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