首页> 外文期刊>Canadian Journal of Animal Science >Whole genome fine mapping of quantitative trait loci for ultrasound and carcass merit traits in beef cattle.
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Whole genome fine mapping of quantitative trait loci for ultrasound and carcass merit traits in beef cattle.

机译:肉牛超声和car体功性状的数量性状基因座的全基因组精细定位。

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Quantitative trait loci (QTL) mapped to large chromosomal regions have limited utility as DNA markers for marker-assisted selection (MAS) and are less informative as a reference for the identification of underlying causative quantitative trait nucleotides (QTN). In this study, whole genome fine mapping of QTL for ultrasound and carcass merit traits in beef cattle was conducted using a greater density of single nucleotide polymorphism (SNP) markers, and SNP markers within the QTL regions associated with the traits were identified. 418 male cattle from 28 sires were used in this study with 9 ultrasound and 7 carcass merit traits that were collected as part of a feedlot trial conducted from 2003 to 2005 at the University of Alberta Kinsella ranch, Canada. Sires and their progeny were genotyped for a total of 4592 SNP markers distributed across all 29 cattle autosomes. Across-family analyses detected 12 QTL for 5 ultrasound traits on 9 chromosomes and 18 QTL for 6 carcass merit traits on 10 chromosomes (P < 0.05). Within-family analyses identified 78 significant QTL for 9 ultrasound and 7 carcass merit traits (P < 0.01). The use of a denser panel of SNP markers allowed fine mapping of QTL to smaller chromosomal regions ranging from 0.6 to 11 cM compared with relatively larger QTL regions of 4-24 cM reported in previous studies. Furthermore, single SNP marker association analyses identified 22 SNP that were significantly associated with 3 ultrasound and 4 carcass merit traits under 12 QTL regions (P < 0.05). These identified SNP markers significantly associated with the traits under the fine mapped QTL regions provide genomic tools for potential application of MAS and a reference to assist with the identification of QTN causing variations in ultrasound and carcass merit traits in beef cattle.
机译:映射到大染色体区域的定量性状基因座(QTL)作为标记辅助选择(MAS)的DNA标记物用途有限,并且不能作为鉴定潜在致病性定量性状核苷酸(QTN)的参考。在这项研究中,使用更高密度的单核苷酸多态性(SNP)标记对肉牛的超声和car体品质性状进行QTL的全基因组精细定位,并鉴定了与性状相关的QTL区域内的SNP标记。 2003年至2005年在加拿大阿尔伯塔省金塞拉大学牧场进行的饲养场试验中,收集了来自28个父亲的418头公牛的9个超声波和7个car体特征。对Sires及其后代进行了基因分型,确定了分布在所有29个牛常染色体上的4592个SNP标记。跨家庭分析检测到9个染色体上的5个超声特征的12个QTL和10个染色体上的6个car体特征的18个QTL( P <0.05)。家庭内部分析确定了针对9个超声和7个car体功绩特征的78个重要QTL( P <0.01)。与先前研究中报道的相对较大的4-24 cM的较大QTL区相比,使用更密集的SNP标记组可以将QTL精细定位在0.6至11 cM的较小染色体区。此外,单个SNP标记关联分析确定了22个SNP,它们与12个QTL区域下的3个超声和4个car体优点显着相关( P <0.05)。这些与精细定位的QTL区域下的性状显着相关的SNP标记物为MAS的潜在应用提供了基因组工具,并为协助鉴定QTN引起了肉牛的超声波和cas体品质性状的变异提供了参考。

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