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首页> 外文期刊>Current Genetics: Eukaryotes with Emphasis on Yeasts, Fungi, Mitochondria, Plastids >FvSNF1 , the sucrose non-fermenting protein kinase gene of Fusarium virguliforme , is required for cell-wall-degrading enzymes expression and sudden death syndrome development in soybean
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FvSNF1 , the sucrose non-fermenting protein kinase gene of Fusarium virguliforme , is required for cell-wall-degrading enzymes expression and sudden death syndrome development in soybean

机译:FUSARIUMVURIFULEE的蔗糖非发酵蛋白激酶基因的FVSNF1是大豆中细胞 - 壁降解酶表达和猝死综合征的培养

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摘要

Abstract Fusarium virguliforme is a soil-borne pathogenic fungus that causes sudden death syndrome (SDS) in soybean. Its pathogenicity is believed to require the activity of cell-wall-degrading enzymes (CWDEs). The sucrose non-fermenting protein kinase 1 gene ( SNF1 ) is a key component of the glucose de-repression pathway in yeast, and a regulator of gene expression for CWDEs in some plant pathogenic fungi. To elucidate the functional role of the SNF1 homolog in F. virguliforme, FvSNF1 was disrupted using a split-marker strategy. Disruption of FvSNF1 in F. virguliforme abolishes galactose utilization and causes poor growth on xylose, arabinose and sucrose. However, the resulting Fvsnf1 mutant grew similar to wild-type and ectopic transformants on glucose, fructose, maltose, or pectin as the main source of carbon. The Fvsnf1 mutant displayed no expression of the gene-encoding galactose oxidase (GAO), a secretory enzyme that catalyzes oxidation of D-galactose. It also exhibited a significant reduction in the expression of several CWDE-coding genes in contrast to the wild-type strain. Greenhouse pathogenicity assays revealed that the Fvsnf1 mutant was severely impaired in its ability to cause SDS on challenged soybean plants. Microscopy and microtome studies on infected roots showed that the Fvsnf1 mutant was defective in colonizing vascular tissue of infected plants. Cross and longitudinal sections of infected roots stained with fluorescein-labeled wheat germ agglutinin and Congo red showed that the Fvsnf1 mutant failed to colonize the xylem vessels and phloem tissue at later stages of infection. Quantification of the fungal biomass in inoculated roots further confirmed a reduced colonization of roots by the Fvsnf1 mutant when compared to the wild type. These findings suggest that FvSNF1 regulates the expression of CWDEs in F. virguliforme , thus affecting the virulence of the fungus on soybean.
机译:摘要镰刀菌毒蕈状是一种土壤传播的致病性真菌,导致大豆猝死综合症(SDS)。认为其致病性需要细胞 - 壁降解酶(CWDES)的活性。蔗糖非发酵蛋白激酶1基因(SNF1)是酵母葡萄糖去抑制途径的关键组分,以及一些植物病原真菌的CWDES的基因表达调节剂。为了阐明SNF1同源物在F.Verguliforme中的功能作用,使用分裂标记策略破坏FVSNF1。 FVSNF1在F.Virguliforme中断的破坏废除半乳糖利用,并导致木糖,阿拉伯糖和蔗糖的生长差。然而,得到的FVSNF1突变体具有类似于葡萄糖,果糖,麦芽糖或果胶的野生型和异位转化体作为碳的主要来源。 FVSNF1突变体显示了编码基因编码的半乳糖氧化酶(GAO)的表达,催化D-半乳糖氧化的分泌酶。与野生型菌株相比,它还表现出几种CWDE编码基因的表达显着降低。温室致病性测定揭示了FVSNF1突变体在其导致挑战大豆植物中的能力中严重受损。感染根部的显微镜和切片体研究表明,FVSNF1突变体在殖民化感染植物的血管组织方面有缺陷。用荧光素标记的小麦胚芽凝集素和刚果红色染色的感染根的交叉和纵向部分表明,FVSNF1突变体未能在稍后的感染阶段定植木质血管和韧皮肌组织。与野生型相比,接种根中的真菌生物质的定量进一步证实了FVSNF1突变体的根部的结肠化。这些发现表明FVSNF1调节F.Virguliforme中CWDES的表达,从而影响大豆对真菌的毒力。

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