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首页> 外文期刊>TAG Theoretical and Applied Genetics >Differential expression of genes in soybean in response to the causal agent of Asian soybean rust (Phakopsora pachyrhizi Sydow) is soybean growth stage-specific
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Differential expression of genes in soybean in response to the causal agent of Asian soybean rust (Phakopsora pachyrhizi Sydow) is soybean growth stage-specific

机译:响应亚洲大豆锈病(Phakopsora pachyrhizi Sydow)的病原体,大豆中基因的差异表达是特定于大豆生长阶段的

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Understanding plant host response to a pathogen such as Phakopsora pachyrhizi, the causal agent of Asian soybean rust (ASR), under different environmental conditions and growth stages is crucial for developing a resistant plant variety. The main objective of this study was to perform global transcriptome profiling of P. pachyrhizi-exposed soybean (Glycine max) with susceptible reaction to the pathogen from two distinct developmental growth stages using whole genome Affymetrix microarrays of soybean followed by confirmation using a resistant genotype. Soybean cv. 5601T (susceptible to ASR) at the V4 and R1 growth stages and Glycine tomentella (resistant to ASR) plants were inoculated with P. pachyrhizi and leaf samples were collected after 72 h of inoculation for microarray analysis. Upon analyzing the data using Array Assist software at 5% false discovery rate (FDR), a total of 5,056 genes were found significantly differentially expressed at V4 growth stage, of which 2,401 were up-regulated, whereas 579 were found differentially expressed at R1 growth stage, of which 264 were up-regulated. There were 333 differentially expressed common genes between the V4 and R1 growth stages, of which 125 were up-regulated. A large difference in number of differentially expressed genes between the two growth stages indicates that the gene expression is growth-stage-specific. We performed real-time RT-PCR analysis on nine of these genes from both growth stages and both plant species and found results to be congruent with those from the microarray analysis.
机译:在不同的环境条件和生长阶段,了解植物寄主对病原体(如亚洲大豆锈病(ASR)的病原体)的致病菌的反应对于开发抗性植物品种至关重要。这项研究的主要目的是使用大豆全基因组Affymetrix微阵列对暴露于P.Pyryrhizi的大豆(Glycine max)进行全局转录组分析,并对来自两个不同发育阶段的病原体进行易感反应,然后使用抗性基因型进行确认。大豆简历在V 4 和R 1 生长阶段对5601T(易受ASR感染)和甘氨酸小肠绒毛球菌(对ASR具有抗性)接种P. pyryrhizi,然后收集叶片样品。接种72小时以进行微阵列分析。使用Array Assist软件以5%的错误发现率(FDR)分析数据后,发现共有5,056个基因在V 4 生长阶段显着差异表达,其中2,401个被上调,而发现579个在R 1 生长阶段差异表达,其中264个被上调。 V 4 和R 1 生长期之间共有333个差异表达的共有基因,其中125个上调。两个生长阶段之间差异表达基因的数量差异很大,表明该基因表达是生长阶段特异性的。我们对来自两个生长阶段和两个植物物种的九个基因进行了实时RT-PCR分析,发现结果与微阵列分析的结果一致。

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