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Induction of a small heat shock protein and its functional roles in Nicotiana plants in the defense response against Ralstonia solanacearum(1[W])

机译:烟草中一种小分子热激蛋白的诱导及其在烟草青枯菌防御反应中的作用(1 [W])

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In tobacco (Nicotiana tabacum), Ralstonia solanacearum OE1-1 (RsOE1-1) is pathogenic, whereas R. solanacearum 8107 (Rs8107) is nonpathogenic and induces the hypersensitive response (HR). To elucidate the molecular mechanisms of plant-R. solanacearum interactions, we used differential display to isolate a cDNA fragment, A6, regulated in tobacco by inoculation with RsOE1-1. The deduced amino acid sequence predicted from full-length A6-cDNA showed similarity to small heat shock proteins from Arabidopsis (Arabidopsis thaliana; hypothetical protein), Medicago truncatula, and Cucumis melo; we therefore designated A6 to correspond to Ntshsp17 (for tobacco small heat shock protein 17). Recombinant Ntshsp17 overproduced in Escherichia coli exhibited molecular chaperone function. Expression of Ntshsp17 was increased in tobacco leaves inoculated with both RsOE1-1 and Rs8107. Expression was induced by heat treatment and by treatment with aminocyclopropane carboxylic acid, hydrogen peroxide, methyl jasmonate, and salicylic acid. Ntshsp17 expression was induced by inoculation with a HR and pathogenicity gene mutant of Rs8107 that does not induce the HR, but not by Agrobacterium-mediated transient expression of INF1, an HR elicitor. In Nbshsp17-silenced plants (an Ntshsp17 ortholog in Nicotiana benthamiana), expression of ETHYLENE-RESPONSE ELEMENT-BINDING PROTEIN, PATHOGENESIS-RELATED1a (PR1a), and PR4 genes was compromised, but expression of ELONGATION FACTOR1 alpha was scarcely affected. Appearance of the HR was not affected in the silenced plants. In the silenced plants, growth of Rs8107 was accelerated. Bacterial growth and wilt symptoms elicited by RsOE1-1 were also accelerated in the silenced plants. These results indicate that this small heat shock protein might have a role in HR-independent defenses in Nicotiana plants.
机译:在烟草(Nicotiana tabacum)中,青枯雷尔氏菌OE1-1(RsOE1-1)具有致病性,而青枯雷尔氏菌8107(Rs8107)是非致病性的,可诱发超敏反应(HR)。阐明植物R的分子机制。茄属植物相互作用,我们使用差异展示来分离通过接种RsOE1-1在烟草中调控的cDNA片段A6。从全长A6-cDNA预测的推导的氨基酸序列显示出与拟南芥(拟南芥;假定蛋白),small藜苜蓿和黄瓜甜瓜的小热激蛋白相似。因此,我们指定A6对应于Ntshsp17(用于烟草小热激蛋白17)。在大肠杆菌中过量产生的重组Ntshsp17具有分子伴侣功能。在同时接种RsOE1-1和Rs8107的烟叶中Ntshsp17的表达增加。通过热处理和用氨基环丙烷羧酸,过氧化氢,茉莉酸甲酯和水杨酸处理诱导表达。 Ntshsp17表达是通过接种不诱导HR的HR和致病性基因突变体Rs8107诱导的,而不是通过农杆菌介导的HR1瞬时表达INF1诱导的。在Nbshsp17沉默的植物中(烟草中的Ntshsp17直系同源基因),乙烯反应元素结合蛋白,与病原相关的1a(PR1a)和PR4基因的表达受到损害,但对ELONGATION FACTOR1α的表达几乎没有影响。在沉默的植物中,HR的外观没有受到影响。在沉默的植物中,Rs8107的生长加速了。在沉默的植物中,RsOE1-1引起的细菌生长和枯萎症状也被加速。这些结果表明,这种小的热激蛋白可能在烟草植物中与HR无关的防御中起作用。

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