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Genome-wide mining seed-specific candidate genes from peanut for promoter cloning

机译:全基因组挖掘花生种子特异性候选基因用于启动子克隆

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摘要

Peanut seeds are ideal bioreactors for the production of foreign recombinant proteins and/or nutrient metabolites. Seed-Specific Promoters (SSPs) are important molecular tools for bioreactor research. However, few SSPs have been characterized in peanut seeds. The mining of Seed-Specific Candidate Genes (SSCGs) is a prerequisite for promoter cloning. Here, we described an approach for the genome-wide mining of SSCGs via comparative gene expression between seed and nonseed tissues. Three hundred thirty-seven SSCGs were ultimately identified, and the top 108 SSCGs were characterized. Gene Ontology (GO) analysis revealed that some SSCGs were involved in seed development, allergens, seed storage and fatty acid metabolism. RY REPEAT and GCN4 motifs, which are commonly found in SSPs, were dispersed throughout most of the promoters of SSCGs. Expression pattern analysis revealed that all 108 SSCGs were expressed specifically or preferentially in the seed. These results indicated that the promoters of the 108 SSCGs may perform functions in a seed-specific and/or seed-preferential manner. Moreover, a novel SSP was cloned and characterized from a paralogous gene of SSCG29 from cultivated peanut. Together with the previously characterized SSP of the SSCG5 paralogous gene in cultivated peanut, these results implied that the method for SSCG identification in this study was feasible and accurate. The SSCGs identified in this work could be widely applied to SSP cloning by other researchers. Additionally, this study identified a low-cost, high-throughput approach for exploring tissue-specific genes in other crop species.
机译:花生种子是生产外源重组蛋白和/或营养代谢产物的理想生物反应器。种子特异性启动子(SSP)是生物反应器研究的重要分子工具。但是,花生种子中很少有SSP的特征。种子特异性候选基因(SSCG)的挖掘是启动子克隆的前提。在这里,我们描述了一种通过种子和非种子组织之间的比较基因表达对SSCG进行全基因组挖掘的方法。最终确定了337个SSCG,并确定了前108个SSCG。基因本体论(GO)分析显示,某些SSCG与种子发育,过敏原,种子贮藏和脂肪酸代谢有关。在SSP中常见的RY REPEAT和GCN4基序分散在大多数SSCG启动子中。表达模式分析表明,所有108种SSCG均在种子中特异性或优先表达。这些结果表明108个SSCG的启动子可以以种子特异性和/或种子优先的方式执行功能。此外,从栽培花生的SSCG29的旁系基因克隆并表征了新的SSP。结合先前鉴定的栽培花生中SSCG5旁系基因的SSP,这些结果表明本研究中的SSCG鉴定方法是可行和准确的。在这项工作中确定的SSCG可以被其他研究人员广泛应用于SSP克隆。此外,这项研究确定了一种低成本,高通量的方法来探索其他作物物种中的组织特异性基因。

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  • 期刊名称 other
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  • 年(卷),期 -1(14),3
  • 年度 -1
  • 页码 e0214025
  • 总页数 21
  • 原文格式 PDF
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