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首页> 外文期刊>Frontiers in Plant Science >RNA-Seq Analysis of Differential Gene Expression Responding to Different Rhizobium Strains in Soybean ( Glycine max) Roots
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RNA-Seq Analysis of Differential Gene Expression Responding to Different Rhizobium Strains in Soybean ( Glycine max) Roots

机译:大豆根茎中不同根瘤菌菌株差异基因表达的RNA-Seq分析

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摘要

The root nodule symbiosis (RNS) between legume plants and rhizobia is the most efficient and productive source of nitrogen fixation, and has critical importance in agriculture and mesology. Soybean ( Glycine max ), one of the most important legume crops in the world, establishes a nitrogen-fixing symbiosis with different types of rhizobia, and the efficiency of symbiotic nitrogen fixation in soybean greatly depends on the symbiotic host-specificity. Although, it has been reported that rhizobia use surface polysaccharides, secretion proteins of the type-three secretion systems and nod factors to modulate host range, the host control of nodulation specificity remains poorly understood. In this report, the soybean roots of two symbiotic systems ( Bradyrhizobium japonicum strain 113-2-soybean and Sinorhizobium fredii USDA205-soybean)with notable different nodulation phenotypes and the control were studied at five different post-inoculation time points (0.5, 7–24 h, 5, 16, and 21 day) by RNA-seq (Quantification). The results of qPCR analysis of 11 randomly-selected genes agreed with transcriptional profile data for 136 out of 165 (82.42%) data points and quality assessment showed that the sequencing library is of quality and reliable. Three comparisons (control vs. 113-2, control vs. USDA205 and USDA205 vs. 113-2) were made and the differentially expressed genes (DEGs) between them were analyzed. The number of DEGs at 16 days post-inoculation (dpi) was the highest in the three comparisons, and most of the DEGs in USDA205 vs. 113-2 were found at 16 dpi and 21 dpi. 44 go function terms in USDA205 vs. 113-2 were analyzed to evaluate the potential functions of the DEGs, and 10 important KEGG pathway enrichment terms were analyzed in the three comparisons. Some important genes induced in response to different strains (113-2 and USDA205) were identified and analyzed, and these genes primarily encoded soybean resistance proteins, NF-related proteins, nodulins and immunity defense proteins, as well as proteins involving flavonoids/flavone/flavonol biosynthesis and plant-pathogen interaction. Besides, 189 candidate genes are largely expressed in roots andor nodules. The DEGs uncovered in this study provides molecular candidates for better understanding the mechanisms of symbiotic host-specificity and explaining the different symbiotic effects between soybean roots inoculated with different strains (113-2 and USDA205).
机译:豆科植物和根瘤菌之间的根瘤共生(RNS)是固氮最有效和最有效的来源,在农业和气象学中具有至关重要的意义。大豆(Glycine max)是世界上最重要的豆类作物之一,建立了具有不同类型根瘤菌的固氮共生关系,大豆中共生固氮的效率在很大程度上取决于共生宿主的特异性。尽管据报道,根瘤菌利用表面多糖,三型分泌系统的分泌蛋白和结节因子来调节宿主范围,但对结节特异性的宿主控制仍知之甚少。在本报告中,研究了两个共生系统(大豆慢生根瘤菌113-2-大豆和弗氏中华根瘤菌USDA205-大豆)的大豆根,它们具有明显不同的结瘤表型,并在五个不同的接种后时间点(0.5、7– 24小时,5、16和21天)通过RNA-seq(定量)。对165个(82.42%)数据点中的136个进行随机选择的11个基因的qPCR分析结果与转录谱数据相符,并且质量评估表明该测序文库质量可靠。进行了三个比较(对照与113-2,对照与USDA205和USDA205与113-2),并分析了它们之间的差异表达基因(DEG)。在三个比较中,接种后第16天的DEG数量最高(dpi),USDA205与113-2中的大多数DEG分别为16 dpi和21 dpi。分析了USDA205与113-2中的44个go函数项,以评估DEG的潜在功能,并在三个比较中分析了10个重要的KEGG途径富集项。鉴定并分析了响应不同菌株(113-2和USDA205)而诱导的一些重要基因,这些基因主要编码大豆抗性蛋白,NF相关蛋白,结节蛋白和免疫防御蛋白,以及涉及类黄酮/黄酮/黄酮醇的生物合成与植物-病原体的相互作用。此外,有189个候选基因在根和/或根瘤中大量表达。在这项研究中发现的DEGs为更好地了解共生宿主特异性机制和解释接种了不同菌株(113-2和USDA205)的大豆根之间的不同共生效应提供了分子候选物。

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