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Understanding Host-Pathogen Interactions with Expression Profiling of NILs Carrying Rice-Blast Resistance Pi9 Gene

机译:了解携带水稻抗稻瘟病Pi9基因的NILs的表达谱与宿主病原体相互作用。

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摘要

Magnaporthe oryzae infection causes rice blast, a destructive disease that is responsible for considerable decrease in rice yield. Development of resistant varieties via introgressing resistance genes with marker-assisted breeding can eliminate pesticide use and minimize crop losses. Here, resistant near-isogenic line (NIL) of Pusa Basmati-1(PB1) carrying broad spectrum rice blast resistance gene Pi9 was used to investigate Pi9-mediated resistance response. Infected and uninfected resistant NIL and susceptible control line were subjected to RNA-Seq. With the exception of one gene (Pi9), transcriptional signatures between the two lines were alike, reflecting basal similarities in their profiles. Resistant and susceptible lines possessed 1043 (727 up-regulated and 316 down-regulated) and 568 (341 up-regulated and 227 down-regulated) unique and significant differentially expressed loci (SDEL), respectively. Pathway analysis revealed higher transcriptional activation of kinases, WRKY, MYB, and ERF transcription factors, JA-ET hormones, chitinases, glycosyl hydrolases, lipid biosynthesis, pathogenesis and secondary metabolism related genes in resistant NIL than susceptible line. Singular enrichment analysis demonstrated that blast resistant NIL is significantly enriched with genes for primary and secondary metabolism, response to biotic stimulus and transcriptional regulation. The co-expression network showed proteins of genes in response to biotic stimulus interacted in a manner unique to resistant NIL upon M. oryzae infection. These data suggest that Pi9 modulates genome-wide transcriptional regulation in resistant NIL but not in susceptible PB1. We successfully used transcriptome profiling to understand the molecular basis of Pi9-mediated resistance mechanisms, identified potential candidate genes involved in early pathogen response and revealed the sophisticated transcriptional reprogramming during rice-M. oryzae interactions.
机译:稻瘟病菌感染会引起稻瘟病,这是一种破坏性疾病,可导致稻米产量大幅下降。通过将抗性基因渗入并通过标记辅助育种来开发抗性品种,可以消除农药的使用并最大程度地减少农作物的损失。在这里,使用带有广谱稻瘟病抗性基因Pi9的Pusa Basmati-1(PB1)的抗近等基因系(NIL)来研究Pi9介导的抗性反应。将感染和未感染的抗性NIL和易感对照系进行RNA-Seq。除了一个基因(Pi9)外,两株系之间的转录特征相似,反映了它们谱中的基础相似性。抗性和易感品系分别具有独特的和显着的差异表达基因座(SDEL),分别具有1043个(上调727个和316个下调)和568个(上调341个而227个下调)。途径分析显示,与易感品系相比,抗性NIL中激酶,WRKY,MYB和ERF转录因子,JA-ET激素,几丁质酶,糖基水解酶,脂质生物合成,发病机制和次级代谢相关基因的转录激活更高。奇异富集分析表明,抗瘟的NIL大量富集了主要和次要代谢,对生物刺激的反应和转录调控的基因。共表达网络显示响应生物刺激的基因蛋白相互作用,这种相互作用以米曲霉感染后抗性NIL特有的方式相互作用。这些数据表明Pi9调节抗性NIL中的全基因组转录调控,但不影响易感的PB1。我们成功地使用转录组分析来了解Pi9介导的抗性机制的分子基础,鉴定了参与早期病原体反应的潜在候选基因,并揭示了水稻M期间复杂的转录重编程。稻米相互作用。

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