首页> 外文期刊>Gene: An International Journal Focusing on Gene Cloning and Gene Structure and Function >Molecular cloning and functional analysis of GbRVd, a gene in Gossypium barbadense that plays an important role in conferring resistance to Verticillium wilt
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Molecular cloning and functional analysis of GbRVd, a gene in Gossypium barbadense that plays an important role in conferring resistance to Verticillium wilt

机译:GbRVd的分子克隆和功能分析,该基因是巴巴德棉中的一个基因,在赋予黄萎病抗性中起重要作用

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Most of the disease resistance genes already characterized in plants encode nucleotide-binding site-leucine rich repeat (NBS-LRR) proteins that have key roles in resistance to Verticillium dahliae. Using a cDNA library and RACE protocols, we cloned a coiled-coil (CC)-NBS-LRR-type gene, GbRVd, from a resistant tetraploid cotton species, Gossypium barbadense (RVd = Resistance to V. dahliae). We also applied RT-qPCR and VIGS technologies to analyze how expression of GbRVd was induced upon attack by V. dahliae. Its 2862-bp ORF encodes a predicted protein containing 953 amino add residues, with a predicted molecular weight of 110.17 kDa and an isoelectric point of 5.87. GbRVd has three domains - CC, NBS, and LRR - and is most closely related to Gossypium raimondii RVd (88% amino acid identity). Profiling demonstrated that GbRVd is constitutively expressed in all tested tissues, and transcript levels are especially high in the leaves. In plants inoculated with V. dahliae, GbRVd was significantly up-regulated when compared with the control, with expression peaking at 48 h post-inoculation. Silencing of GbRVd in cotton through VIGS dramatically down-regulated SA, NO, and H2O2 production, resulting in greater susceptibility to V. dahliae. Taken together, these results suggest that GbRVd has an important role in protecting G. barbadense against infection by V. dahliae. (C) 2015 Elsevier B.V. All rights reserved.
机译:植物中已经鉴定的大多数抗病基因都编码核苷酸结合位点-富含亮氨酸的重复序列(NBS-LRR)蛋白,这些蛋白在对黄萎病菌的抗性中具有关键作用。使用cDNA文库和RACE协议,我们从抗性四倍体棉种Gossypium barbadense(RVd =抗大麦草)克隆了卷曲螺旋(CC)-NBS-LRR型基因GbRVd。我们还应用了RT-qPCR和VIGS技术来分析大丽花叶病毒攻击后如何诱导GbRVd的表达。它的2862 bp ORF编码一个预测的蛋白质,该蛋白质包含953个氨基酸残基,预测分子量为110.17 kDa,等电点为5.87。 GbRVd具有三个域-CC,NBS和LRR,并且与雷蒙氏棉RVd(88%的氨基酸同一性)关系最密切。分析表明,GbRVd在所有测试的组织中组成性表达,并且叶片中的转录水平特别高。与对照相比,在接种了大黄弧菌的植物中,GbRVd显着上调,在接种后48小时表达达到峰值。通过VIGS使棉花中的GbRVd沉默,从而显着下调了SA,NO和H2O2的产生,从而导致对大麦弧菌的敏感性更高。综上所述,这些结果表明,GbRVd在保护巴巴氏假丝酵母免受大麦弧菌感染方面具有重要作用。 (C)2015 Elsevier B.V.保留所有权利。

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