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Genetic transformation of durum wheat for resistance to fungal pathogens.

机译:杜兰姆小麦抗性病原体耐药遗传转化。

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Transgenic technology is routinely used to genetically modify durum wheat for different aims. Among these; the introduction of defense genes against fungal pathogens is of major interest. The commercial durum wheat variety Ofanto was stably transformed by bombardment of immature inflorescences using the plasmid pMM3; containing the expression cassette pRbcs-^52 as tool to confer resistance to fungal pathogens. The b-32 protein is a maize cytosolic albumin with a molecular weight of 32 kDa; synthesized in temporal and quantitative coordination with the storage proteins in the endosperm; molecularly homologous and enzymatically acting as a functional ribosome-inactivating protein (RIP). Three indipendent transformed lines were obtained using the cv.Ofanto; and the primary events were crossed with parental non-transformed Ofanto; in order to avoid somaclonal variation effects; until F3 generations. The presence of gene b32 and of its transcripts in the leaves of transgenic plants is shown by means of PCR and RT-PCR experiments. The molecular characterisation of these lines is presented. In vivo analysis of homozygous lines in pathogenicity assays; in order to assess the effects of b-32 upon fungal infection; is in progress.
机译:转基因技术通常用于转基因杜兰姆小麦以进行不同的目的。在这些当中;防御基因对真菌病原体的引入是主要的兴趣。使用质粒PMM3轰击不成熟的花序轰击商业硬粒小麦品种稳定转化;含有表达盒PRBCS-^ 52作为赋予真菌病原体抗性的工具。 B-32蛋白是玉米胞质白蛋白,分子量为32kDa;用胚乳中的储存蛋白质在时间和定量协调中合成;分子同源和酶促作用作为功能性核糖体灭活蛋白(RIP)。使用CV.OfAlo获得三条润级转化线;并且主要事件与父母非转化的父母非转化;为了避免糖蜜变化效应;直到F3代。通过PCR和RT-PCR实验显示基因B32和转基因植物叶片中的其转录物的存在。提出了这些线的分子表征。在致病性测定中的纯合子中的体内分析;为了评估B-32对真菌感染的影响;正在处理。

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