首页> 外文期刊>Frontiers in Plant Science >A Simple and Efficient Approach to Elucidate Genomic Contribution of Transcripts to a Target Gene in Polyploids: The Case of Hexaploid Wheat ( Triticum aestivum L.)
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A Simple and Efficient Approach to Elucidate Genomic Contribution of Transcripts to a Target Gene in Polyploids: The Case of Hexaploid Wheat ( Triticum aestivum L.)

机译:阐明转录本对多倍体中靶基因的基因组贡献的简单有效方法:以六倍体小麦为例(普通小麦 L。)

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Common wheat ( Triticum aestivum L.) is one of the most economically important crops in the world, however, gene functional studies in this crop have been lagging mainly due to the complexity of its polyploid genome, which is derived through two rounds of intergeneric hybridization events that led to the presence of six copies for each gene. Elucidating the transcript contribution of each genome to the total expression of a target gene in polyploids such as hexaploid wheat has a paramount significance for direct discovery of genes and the associated molecular mechanisms controlling traits of agronomic importance. A polymerase chain reaction approach that involved primers amplifying DNA fragments unique to each homeolog of a target gene and quantitation of the intensity of the resulting fragment bands were able to successfully determine the genomic transcript contributions as a percentage of target gene's total expression in hexaploid wheat. Our results showed that the genomic contributions of transcripts to a target gene vary with genotype and tissue type, suggesting the distinct role of each homeolog in regulating the trait associated with the target gene. The approach described in this study is an effective and economical method to elucidate the genomic transcript contribution to the total expression of individual target genes in hexaploid wheat. It can also be applied to determine the transcript contribution of each genome towards the collective expression of a target gene in other economically important polypoid crop species.
机译:普通小麦(Triticum aestivum L.)是世界上最重要的经济作物之一,然而,该作物的基因功能研究滞后,主要是由于其多倍体基因组的复杂性,这是通过两轮基因间杂交获得的导致每个基因有六个拷贝的事件。阐明每个基因组对多倍体(如六倍体小麦)中靶基因总表达的转录本贡献,对于直接发现基因和控制农艺重要性状的相关分子机制至关重要。一种聚合酶链反应方法,其中涉及的引物可扩增靶基因每个同源基因特有的DNA片段,并对所得片段条带的强度进行定量,从而能够成功确定基因组转录本的贡献,占靶基因在六倍体小麦中总表达量的百分比。我们的结果表明,转录本对目标基因的基因组贡献随基因型和组织类型的不同而变化,表明每种同源物在调节与目标基因相关的性状中的独特作用。本研究中描述的方法是阐明六倍体小麦中基因组转录本对单个目标基因总表达的贡献的一种有效且经济的方法。它也可用于确定每个基因组对目标基因在其他经济上重要的息肉类作物物种中的集体表达的转录本贡献。

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