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首页> 外文期刊>Plant Biotechnology Journal >Integrated transcriptome, small RNA and degradome sequencing approaches provide insights into Ascochyta blight resistance in chickpea
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Integrated transcriptome, small RNA and degradome sequencing approaches provide insights into Ascochyta blight resistance in chickpea

机译:集成的转录组,小RNA和降低测量方法在鹰嘴豆中提供了对Ascochyta的抗性的见解

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Ascochyta blight (AB) is one of the major biotic stresses known to limit the chickpea production worldwide. To dissect the complex mechanisms of AB resistance in chickpea, three approaches, namely, transcriptome, small RNA and degradome sequencing were used. The transcriptome sequencing of 20 samples including two resistant genotypes, two susceptible genotypes and one introgression line under control and stress conditions at two time points (3rd and 7th day post inoculation) identified a total of 6767 differentially expressed genes (DEGs). These DEGs were mainly related to pathogenesis‐related proteins, disease resistance genes like NBS‐LRR, cell wall biosynthesis and various secondary metabolite synthesis genes. The small RNA sequencing of the samples resulted in the identification of 651 miRNAs which included 478 known and 173 novel miRNAs. A total of 297 miRNAs were differentially expressed between different genotypes, conditions and time points. Using degradome sequencing and in silico approaches, 2131 targets were predicted for 629 miRNAs. The combined analysis of both small RNA and transcriptome datasets identified 12 miRNA‐mRNA interaction pairs that exhibited contrasting expression in resistant and susceptible genotypes and also, a subset of genes that might be post‐transcriptionally silenced during AB infection. The comprehensive integrated analysis in the study provides better insights into the transcriptome dynamics and regulatory network components associated with AB stress in chickpea and, also offers candidate genes for chickpea improvement.
机译:ascochyta枯萎(ab)是已知的主要生物应力之一,以限制全球鹰嘴豆生产。解剖鹰嘴豆术中AB抗性的复杂机制,使用三种方法,即转录组,小RNA和降低组测序。 20个样品的转录组测序包括两个抗性基因型,两个易感基因型和在两个时间点(第7天接种后的胁迫条件下的一个易感性基因型和一个血频突出线)鉴定了总共6767个差异表达基因(DEGS)。这些液体主要与发病性相关的蛋白质,抗病基因,如NBS-LRR,细胞壁生物合成等各种次级代谢物合成基因。样品的小RNA测序导致鉴定为651 miRNA,其中包括478名已知和173个新的miRNA。在不同的基因型,条件和时间点之间,总共297 miRNA差异表达。使用降低体测序和硅方法,预测2131个目标629 miRNA。小RNA和转录组数据集的组合分析鉴定了12个miRNA-mRNA相互作用对,其表现出抗性和易感基因型的对比表达,以及在AB感染期间可能在AB感染后沉默的基因子集。该研究的全面综合分析提供了更好的见解,对鹰嘴豆中的AB胁迫相关的转录组动力和调节网络组分提供了更好的见解,并为鹰嘴豆改进提供候选基因。

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