首页> 美国卫生研究院文献>DNA Research: An International Journal for Rapid Publication of Reports on Genes and Genomes >An efficient approach for the development of genome-specific markers in allohexaploid wheat (Triticum aestivum L.) and its application in the construction of high-density linkage maps of the D genome
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An efficient approach for the development of genome-specific markers in allohexaploid wheat (Triticum aestivum L.) and its application in the construction of high-density linkage maps of the D genome

机译:一种开发异源六倍体小麦(Triticum aestivum L.)基因组特异性标记的有效方法及其在构建D基因组高密度连锁图上的应用

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摘要

In common wheat, the development of genotyping platforms has been hampered by the large size of the genome, its highly repetitive elements and its allohexaploid nature. However, recent advances in sequencing technology provide opportunities to resolve these difficulties. Using next-generation sequencing and gene-targeting sequence capture, 12,551 nucleotide polymorphisms were detected in the common wheat varieties ‘Hatsumochi’ and ‘Kitahonami’ and were assigned to chromosome arms using International Wheat Genome Sequencing Consortium survey sequences. Because the number of markers for D genome chromosomes in commercially available wheat single nucleotide polymorphism arrays is insufficient, we developed markers using a genome-specific amplicon sequencing strategy. Approximately 80% of the designed primers successfully amplified D genome-specific products, suggesting that by concentrating on a specific subgenome, we were able to design successful markers as efficiently as could be done in a diploid species. The newly developed markers were uniformly distributed across the D genome and greatly extended the total coverage. Polymorphisms were surveyed in six varieties, and 31,542 polymorphic sites and 5,986 potential marker sites were detected in the D genome. The marker development and genotyping strategies are cost effective, robust and flexible and may enhance multi-sample studies in the post-genomic era in wheat.
机译:在普通小麦中,基因型分型平台的发展因基因组的大尺寸,其高度重复的元件及其异六倍体性质而受到阻碍。但是,测序技术的最新进展为解决这些难题提供了机会。使用下一代测序和基因靶向序列捕获技术,在普通小麦品种“ Hatsumochi”和“ Kitahonami”中检测到12,551个核苷酸多态性,并使用国际小麦基因组测序联盟调查序列将其分配给染色体臂。由于市售小麦单核苷酸多态性阵列中D基因组染色体标记的数量不足,我们使用基因组特异性扩增子测序策略开发了标记。大约80%的设计引物成功扩增了D基因组特异性产物,这表明通过集中于特定的亚基因组,我们能够像在二倍体物种中一样高效地设计成功的标记。新开发的标记在D基因组中均匀分布,并大大扩展了总覆盖范围。调查了六个品种的多态性,在D基因组中检测到31,542个多态性位点和5,986个潜在标记位点。标记物的开发和基因分型策略具有成本效益,稳健且灵活,并且可以增强小麦后基因组时代的多样本研究。

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