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Soybean Seed Amino Acid Content QTL Detected Using the Universal Soy Linkage Panel 1.0 with 1,536 SNPs

机译:使用通用大豆连接板1.0和1,536个sNp检测大豆种子氨基酸含量QTL

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摘要

Soybean [Glycine max (L.) Merr.] is the primary source of meal used in animal feed in the U.S. However, few studies have been conducted to evaluate genomic regions controlling amino acid composition is soybean. Designing soybean seed compositions that will benefit animal production is essential. The objective of this study was to identify genomic regions controlling essential and non-essential amino acid composition in soybean seed proteins. To achieve this objective, 282 F5:9 recombinant inbred lines (RILs) developed from a cross of Essex × Williams 82 were used. Ground soybean seed samples were analyzed for amino acids and statistically significant differences (p \u3c 0.05) were found among genotypes in the population for all amino acid concentrations. The Universal Soy Linkage Panel (USLP) 1.0 of 1,536 single nucleotide polymorphism (SNP) DNA markers were used to genotype the 282 RILs and identify 480 useful genetic markers. The software R/qtl was used to identify candidate quantitative trait loci (QTL), which were validated using R/MQM. A total of ten QTL were detected on chromosomes 5, 7, 9, 10, 13 and 20 that explained 5 to 14% of the total phenotypic variation for a particular amino acid. Using SNPs from the USLP 1.0 to detect QTL for amino acids in soybean provides additional information to select genotypes with enhanced amino acid profiles that will benefit animal production.
机译:大豆[Glycine max(L.)Merr。]是美国动物饲料中使用的主要粗粉。但是,很少有研究评估控制大豆氨基酸组成的基因组区域。设计有益于动物生产的大豆种子组合物至关重要。这项研究的目的是确定控制大豆种子蛋白中必需氨基酸和非必需氨基酸组成的基因组区域。为了实现这一目标,使用了由Essex×Williams 82杂交产生的282个F5:9重组自交系(RIL)。分析了磨碎的大豆种子样品中的氨基酸,发现在所有氨基酸浓度的种群中,基因型之间存在统计学上的显着差异(p <0.05)。 1,536个单核苷酸多态性(SNP)DNA标记的通用大豆连锁专家组(USLP)1.0用于对282个RIL进行基因分型,并鉴定480个有用的遗传标记。使用软件R / qtl来识别候选定量特征位点(QTL),并使用R / MQM对其进行了验证。在5号,7号,9号,10号,13号和20号染色体上总共检测到10个QTL,这解释了特定氨基酸总表型变异的5%至14%。使用USLP 1.0中的SNP检测大豆中氨基酸的QTL提供了更多信息,以选择具有增强的氨基酸谱的基因型,这将有利于动物生产。

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