首页> 美国卫生研究院文献>Frontiers in Microbiology >In planta Identification of Putative Pathogenicity Factors from the Chickpea Pathogen Ascochyta rabiei by De novo Transcriptome Sequencing Using RNA-Seq and Massive Analysis of cDNA Ends
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In planta Identification of Putative Pathogenicity Factors from the Chickpea Pathogen Ascochyta rabiei by De novo Transcriptome Sequencing Using RNA-Seq and Massive Analysis of cDNA Ends

机译:在植物中使用RNA-Seq从头转录组测序和cDNA末端大量分析鉴定鹰嘴豆病原体Ascochyta rabiei的假定致病因子

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摘要

The most important foliar diseases in legumes worldwide are ascochyta blights. Up to now, in the Ascochyta-legume pathosystem most studies focused on the identification of resistance genes in the host, while very little is known about the pathogenicity factors of the fungal pathogen. Moreover, available data were often obtained from fungi growing under artificial conditions. Therefore, in this study we aimed at the identification of the pathogenicity factors of Ascochyta rabiei, causing ascochyta blight in chickpea. To identify potential fungal pathogenicity factors, we employed RNA-seq and Massive Analysis of cDNA Ends (MACE) to produce comprehensive expression profiles of A. rabiei genes isolated either from the fungus growing in absence of its host or from fungi infecting chickpea leaves. We further provide a comprehensive de novo assembly of the A. rabiei transcriptome comprising 22,725 contigs with an average length of 1178 bp. Since pathogenicity factors are usually secreted, we predicted the A. rabiei secretome, yielding 550 putatively secreted proteins. MACE identified 596 transcripts that were up-regulated during infection. An analysis of these genes identified a collection of candidate pathogenicity factors and unraveled the pathogen's strategy for infecting its host.
机译:世界范围内豆科植物中最重要的叶面疾病是草枯病。迄今为止,在Ascochyta-豆科植物病原体系统中,大多数研究集中于鉴定宿主中的抗性基因,而对真菌病原体的致病性因素知之甚少。此外,通常可从人工条件下生长的真菌获得可用数据。因此,在这项研究中,我们旨在鉴定引起鹰嘴豆枯萎病的狂犬病Ascochyta rabiei的致病因素。为了鉴定潜在的真菌致病性因子,我们使用RNA序列和cDNA末端大规模分析(MACE)来产生从不存在宿主的真菌中或感染鹰嘴豆叶片的真菌中分离出的狂犬曲霉基因的全面表达谱。我们进一步提供了由A. rabiei转录组组成的全面的从头组装,包括22,725个重叠群,平均长度为1178 bp。由于通常会分泌致病性因子,因此我们预测了A. rabiei分泌组,产生了550个假定分泌的蛋白质。 MACE确定了596个在感染过程中上调的转录本。对这些基因的分析确定了候选致病因素的集合,并阐明了病原体感染宿主的策略。

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