Nordic Seed A/S: Grindsnabevej 25, 8300 Odder, Denmark.
Department of Agroecology, Faculty of Technology, Aarhus University, Forsøgsvej 1, Flakkebjerg, DK-4200 Slagelse, Denmark.
Int J Mol Sci. 2020 Oct 8;21(19):7418. doi: 10.3390/ijms21197418.
Detoxification of fusariotoxin is a type V Fusarium head blight (FHB) resistance and is considered a component of type II resistance, which is related to the spread of infection within spikes. Understanding this type of resistance is vital for FHB resistance, but to date, nothing is known about candidate genes that confer this resistance in rye due to scarce genomic resources. In this study, we generated a transcriptomic resource. The molecular response was mined through a comprehensive transcriptomic analysis of two rye hybrids differing in the build-up of fusariotoxin contents in grain upon pathogen infection. Gene mining identified candidate genes and pathways contributing to the detoxification of fusariotoxins in rye. Moreover, we found regulatory elements in the promoters of identified genes and linked them to transcription factors. In the fusariotoxin analysis, we found that grain from the Nordic seed rye hybrid "Helltop" accumulated 4 times higher concentrations of deoxynivalenol (DON), 9 times higher nivalenol (NIV), and 28 times higher of zearalenone (ZEN) than that of the hybrid "DH372" after artificial inoculation under field conditions. In the transcriptome analysis, we identified 6675 and 5151 differentially expressed genes (DEGs) in DH372 and Helltop, respectively, compared to non-inoculated control plants. A Kyoto Encyclopedia of Genes and Genomes (KEGG) analysis revealed that DEGs were associated with glycolysis and the mechanistic target of rapamycin (mTOR) signaling pathway in Helltop, whereas carbon fixation in photosynthesis organisms were represented in DH372. The gene ontology (GO) enrichment and gene set enrichment analysis (GSEA) of DEGs lead to identification of the metabolic and biosynthetic processes of peptides and amides in DH372, whereas photosynthesis, negative regulation of catalytic activity, and protein-chromophore linkage were the significant pathways in Helltop. In the process of gene mining, we found four genes that were known to be involved in FHB resistance in wheat and that were differentially expressed after infection only in DH372 but not in Helltop. Based on our results, we assume that DH372 employed a specific response to pathogen infection that led to detoxification of fusariotoxin and prevented their accumulation in grain. Our results indicate that DH372 might resist the accumulation of fusariotoxin through activation of the glycolysis and drug metabolism via cytochrome P450. The identified genes in DH372 might be regulated by the WRKY family transcription factors as associated regulatory elements found in the in silico analysis. The results of this study will help rye breeders to develop strategies against type V FHB.
真菌毒素解毒是一种类型 V 镰刀菌穗腐病(FHB)抗性,被认为是类型 II 抗性的一个组成部分,与穗内感染的传播有关。了解这种抗性对于 FHB 抗性至关重要,但由于基因组资源稀缺,迄今为止,由于缺乏基因组资源,人们对赋予黑麦这种抗性的候选基因知之甚少。在这项研究中,我们生成了一个转录组资源。通过对两种黑麦杂种进行全面的转录组分析,研究了它们在病原体感染后谷物中真菌毒素含量增加方面的分子反应。基因挖掘鉴定了候选基因和途径,这些基因和途径有助于黑麦中真菌毒素的解毒。此外,我们在鉴定基因的启动子中发现了调节元件,并将它们与转录因子联系起来。在真菌毒素分析中,我们发现经过人工接种后,北欧种子黑麦杂种“Helltop”的谷物中脱氧雪腐镰刀菌烯醇(DON)的浓度比杂种“DH372”高 4 倍,雪腐镰刀菌烯醇(NIV)高 9 倍,玉米赤霉烯酮(ZEN)高 28 倍。在转录组分析中,与未接种对照植物相比,DH372 和 Helltop 分别有 6675 个和 5151 个差异表达基因(DEGs)。京都基因与基因组百科全书(KEGG)分析表明,DH372 中 DEGs 与糖酵解和雷帕霉素(mTOR)信号通路有关,而光合作用生物体中的碳固定则在 Helltop 中得到体现。DEGs 的基因本体论(GO)富集和基因集富集分析(GSEA)导致鉴定了 DH372 中肽和酰胺的代谢和生物合成过程,而 Helltop 中的光合作用、催化活性的负调控和蛋白质-发色团连接则是显著途径。在基因挖掘过程中,我们发现了四个在小麦中已知与 FHB 抗性有关的基因,这些基因在感染后仅在 DH372 中差异表达,而在 Helltop 中则没有。基于我们的结果,我们假设 DH372 采用了一种特定的病原体感染反应,导致真菌毒素解毒,并防止其在谷物中积累。我们的结果表明,DH372 可能通过激活糖酵解和细胞色素 P450 介导的药物代谢来抵抗真菌毒素的积累。DH372 中鉴定的基因可能受到 WRKY 家族转录因子的调控,因为在计算机分析中发现了相关的调节元件。这项研究的结果将有助于黑麦育种者制定针对 V 型 FHB 的策略。