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Cloning and characterization of the Gossypium hirsutum major latex protein gene and functional analysis in Arabidopsis thaliana

机译:拟南芥主要乳胶蛋白基因的克隆,鉴定及功能分析

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The major latex protein (MLP) gene in Gossypium hirsutum was cloned and designated Gh-MLP. Expression in cotton root was induced by salt stress and Verticillium dahliae toxin, and bioinformatic analysis showed that Gh-MLP encodes a 157-amino acid protein that is similar to members of the MLP subfamily in the Bet v 1 family. Although the structure of MLP is similar to Bet v 1 family proteins, the sequence identity to other subfamilies of Bet v 1 proteins is less than 20%. The Gh-MLP promoter contains potential cis-acting elements for response to salt stress and fungal elicitor. RT-PCR analysis showed that Gh-MLP expression was rapidly induced by NaCl and V. dahliae toxin, and induction was maintained over 72 h. However, Gh-MLP transgenic Arabidopsis thaliana did not show resistance to V. dahiae, salt tolerance was significantly enhanced. In contrast to the wild type, the Gh-MLP transgene allowed plants to germinate normally after treatment with 75 mM NaCl. Total flavonoid was twofold higher in transgenic Arabidopsis than in the control, suggesting that Gh-MLP might be involved in altering flavonoid content. We hypothesize Gh-MLP, like other Bet v 1 family proteins, participates in the binding or transport of ligands through its specific three-dimensional structure, and takes part in defensive responses to biotic and abiotic stresses. Keywords Flavonoid - Induce expression - Major latex proteins - Salt stress - Verticillium wilt resistance
机译:克隆了陆地棉中的主要乳胶蛋白(MLP)基因,并将其命名为Gh-MLP。盐胁迫和黄萎病菌毒素诱导了棉花根中的表达,生物信息学分析表明,Gh-MLP编码一个157个氨基酸的蛋白质,与Bet v 1家族的MLP亚家族的成员相似。尽管MLP的结构类似于Bet v 1家族蛋白,但与Bet v 1蛋白其他亚家族的序列同一性小于20%。 Gh-MLP启动子包含潜在的顺式作用元件,用于响应盐胁迫和真菌引发剂。 RT-PCR分析显示,NaCl和大丽花弧菌毒素可快​​速诱导Gh-MLP表达,并持续诱导72 h。然而,Gh-MLP转基因拟南芥没有显示出对大叶弧菌的抗性,耐盐性显着增强。与野生型相反,Gh-MLP转基因使植物在用75 mM NaCl处理后能够正常发芽。转基因拟南芥中的总黄酮比对照高两倍,表明Gh-MLP可能参与了黄酮含量的改变。我们假设Gh-MLP与其他Bet v 1家族蛋白一样,通过其特定的三维结构参与配体的结合或转运,并参与对生物和非生物胁迫的防御反应。黄酮类化合物-诱导表达-主要乳胶蛋白-盐胁迫-黄萎病抗性

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