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Transcriptomic profiling and analysis of differentially expressed genes in asparagus bean (Vigna unguiculata ssp. sesquipedalis) under salt stress

机译:盐胁迫下芦笋豆的转录组分析和差异表达基因分析

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摘要

Asparagus bean (Vigna unguiculata ssp. sesquipedalis) is a warm season legume which is widely distributed over subtropical regions and semiarid areas. It is mainly grown as a significant protein source in developing countries. Salinity, as one of the main abiotic stress factors, constrains the normal growth and yield of asparagus bean. This study used two cultivars (a salt-sensitive genotype and a salt-tolerant genotype) under salt stress vs. control to identify salt-stress-induced genes in asparagus bean using RNA sequencing. A total of 692,086,838 high-quality clean reads, assigned to 121,138 unigenes, were obtained from control and salt-treated libraries. Then, 216 root-derived DEGs (differentially expressed genes) and 127 leaf-derived DEGs were identified under salt stress between the two cultivars. Of these DEGs, thirteen were assigned to six transcription factors (TFs), including AP2/EREBP, CCHC(Zn), C2H2, WRKY, WD40-like and LIM. GO analysis indicated four DEGs might take effects on the “oxidation reduction”, “transport” and “signal transduction” process. Moreover, expression of nine randomly-chosen DEGs was verified by quantitative real-time-PCR (qRT-PCR) analysis. Predicted function of the nine tested DEGs was mainly involved in the KEGG pathway of cation transport, response to osmotic stress, and phosphorelay signal transduction system. A salt-stress-related pathway of “SNARE interactions in vesicular transport” was concerned. As byproducts, 15, 321 microsatellite markers were found in all the unigenes, and 17 SNP linked to six salt-stress induced DEGs were revealed. These candidate genes provide novel insights for understanding the salt tolerance mechanism of asparagus bean in the future.
机译:芦笋豆(Vigna unguiculata ssp。sesquipedalis)是一种暖季豆类,广泛分布于亚热带地区和半干旱地区。在发展中国家,它主要作为重要的蛋白质来源而生长。盐度是主要的非生物胁迫因素之一,限制了芦笋豆的正常生长和产量。这项研究使用两个栽培品种(盐敏感基因型和耐盐基因型)在盐胁迫与对照条件下使用RNA测序鉴定芦笋豆中盐胁迫诱导的基因。从对照和盐处理的文库中获得了总计692,086,838个高质量的干净读段,分配给121,138个单基因。然后,在两个品种之间的盐胁迫下鉴定了216个根衍生的DEG(差异表达基因)和127个叶衍生的DEG。在这些DEG中,有13个被分配给六个转录因子(TF),包括AP2 / EREBP,CCHC(Zn),C2H2,WRKY,WD40-like和LIM。 GO分析表明,四种DEG可能会对“氧化还原”,“运输”和“信号转导”过程产生影响。此外,通过定量实时PCR(qRT-PCR)分析验证了九种随机选择的DEG的表达。九种测试DEGs的预测功能主要涉及阳离子转运的KEGG途径,对渗透压的响应以及磷信号传导系统。与盐胁迫有关的途径“囊泡运输中的SNARE相互作用”有关。作为副产物,在所有单基因中发现15个,321个微卫星标记,并揭示了与六个盐胁迫诱导的DEG相关的17个SNP。这些候选基因为将来了解芦笋豆的耐盐机理提供了新颖的见解。

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