首页> 外文期刊>Frontiers in Plant Science >De novo assembly of the Japanese lawngrass ( Zoysia japonica Steud.) root transcriptome and identification of candidate unigenes related to early responses under salt stress
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De novo assembly of the Japanese lawngrass ( Zoysia japonica Steud.) root transcriptome and identification of candidate unigenes related to early responses under salt stress

机译:盐草根系的 De novo 组装和盐胁迫下与早期响应相关的候选单基因的鉴定

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Japanese lawngrass ( Zoysia japonica Steud.) is an important warm-season turfgrass that is able to survive in a range of soils, from infertile sands to clays, and to grow well under saline conditions. However, little is known about the molecular mechanisms involved in its resistance to salt stress. Here, we used high-throughput RNA sequencing (RNA-seq) to investigate the changes in gene expression of Zoysia grass at high NaCl concentrations. We first constructed two sequencing libraries, including control and NaCl-treated samples, and sequenced them using the Illumina HiSeq? 2000 platform. Approximately 157.20 million paired-end reads with a total length of 68.68 Mb were obtained. Subsequently, 32,849 unigenes with an N50 length of 1781 bp were assembled using Trinity. Furthermore, three public databases, the Kyoto Encyclopedia of Genes and Genomes (KEGG), Swiss-prot, and Clusters of Orthologous Groups (COGs), were used for gene function analysis and enrichment. The annotated genes included 57 Gene Ontology (GO) terms, 120 KEGG pathways, and 24 COGs. Compared with the control, 1455 genes were significantly different (false discovery rate ≤0.01, |log_(2)Ratio |≥1) in the NaCl-treated samples. These genes were enriched in 10 KEGG pathways and 73 GO terms, and subjected to 25 COG categories. Using high-throughput next-generation sequencing, we built a database as a global transcript resource for Z. japonica Steud. roots. The results of this study will advance our understanding of the early salt response in Japanese lawngrass roots.
机译:日本草皮草(Zoysia japonica Steud。)是一种重要的暖季型草皮草,能够在从不育沙子到黏土的各种土壤中生存,并在盐分条件下生长良好。然而,关于其抗盐胁迫的分子机制知之甚少。在这里,我们使用高通量RNA测序(RNA-seq)来研究高NaCl浓度下结缕草的基因表达变化。我们首先构建了两个测序文库,包括对照和NaCl处理的样品,然后使用Illumina HiSeq?对其进行了测序。 2000平台。获得了大约1.5720亿对配对读段,总长度为68.68 Mb。随后,使用Trinity组装了32849个N50长度为1781 bp的单基因。此外,三个公共数据库,《京都基因与基因组百科全书》(KEGG),《瑞士保护组织》和直系同源簇(COG),被用于基因功能分析和富集。带注释的基因包括57个基因本体论(GO)术语,120个KEGG通路和24个COG。与对照组相比,在NaCl处理的样品中有1455个基因存在显着差异(错误发现率≤0.01,| log_(2)比率|≥1)。这些基因富含10条KEGG途径和73个GO项,并属于25个COG类别。使用高通量的下一代测序,我们建立了一个数据库,作为Z. japonica Steud的全球转录本资源。根。这项研究的结果将增进我们对日本草坪草根部早期盐响应的理解。

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