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首页> 外文期刊>Phytopathology >Insertional Mutagenesis and Cloning of the Gene Required for the Biosynthesis of the Non-Host-Specific Toxin in Cochliobolus lunatus that Causes Maize Leaf Spot
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Insertional Mutagenesis and Cloning of the Gene Required for the Biosynthesis of the Non-Host-Specific Toxin in Cochliobolus lunatus that Causes Maize Leaf Spot

机译:插入诱变和克隆引起玉米叶斑斑点病的非宿主特异性毒素的生物合成所需基因的克隆。

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摘要

The maize pathotype Cochliobolus lunatus causes Curvularia leaf spot by producing a non-host-specific toxin known as methyl 5-(hydroxymethyl) furan-2-carboxylate (M5HF2C). However, related research that explores the genes that control the production of this toxin is rare. In the current work, Agrobacterium tumefaciens-mediated transformation (ATMT) was employed to tag the gene required for the biosynthesis of the toxin. Of the 3,000 ATMT transformants recovered, 4 showed a significant decline in pathogenicity on maize leaves; 1 transformant, T806, produced no detectable M5HF2C. Genomic DNA that flanks the integrated plasmid was recovered from one of the mutants. A cosmid clone of the wild-type strain was isolated using the recovered DNA as a probe. The results of the structural and functional analyses of the region corresponding to the tagged site were then used as a basis to successfully clone one gene, called Clt-1. Bioinformatics analysis showed that the gene coded a BTB domain-containing protein that comprises 745 amino acids. Southern analysis revealed that the gene was localized in the genome as a single copy. The essential roles of Clt-1 in both toxin production and pathogenicity were confirmed by gene disruption experiments. In summary, the novel gene Clt-1 is closely associated with toxin production and pathogen virulence in leaves of susceptible varieties.
机译:玉米致病菌Cochliobolus lunatus通过产生一种非寄主特异性毒素5-(羟甲基)呋喃-2-羧酸甲酯(M5HF2C)来引起弯孢菌叶斑病。但是,探索控制这种毒素产生的基因的相关研究很少。在当前的工作中,根癌农杆菌介导的转化(ATMT)被用来标记毒素生物合成所需的基因。在回收的3,000个ATMT转化子中,有4个显示出玉米叶片的致病性显着下降。 1个转化子T806没有产生可检测的M5HF2C。从突变体之一中回收了位于整合质粒两侧的基因组DNA。使用回收的DNA作为探针分离野生型菌株的粘粒克隆。然后,将与标记位点相对应的区域的结构和功能分析的结果用作成功克隆一个称为Clt-1的基因的基础。生物信息学分析表明,该基因编码了一个包含745个氨基酸的BTB结构域蛋白。 Southern分析表明该基因以单拷贝形式存在于基因组中。基因破坏实验证实了Clt-1在毒素产生和致病性中的重要作用。总之,新基因Clt-1与易感品种叶片中的毒素产生和病原体毒力密切相关。

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