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Genetic association of marbling score with intragenic nucleotide variants at selection signals of the bovine genome

机译:牛基因组选择信号上大理石花纹得分与基因内核苷酸变异的遗传关联

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摘要

Selection signals of Korean cattle might be attributed largely to artificial selection for meat quality. Rapidly increased intragenic markers of newly annotated genes in the bovine genome would help overcome limited findings of genetic markers associated with meat quality at the selection signals in a previous study. The present study examined genetic associations of marbling score (MS) with intragenic nucleotide variants at selection signals of Korean cattle. A total of 39 092 nucleotide variants of 407 Korean cattle were utilized in the association analysis. A total of 129 variants were selected within newly annotated genes in the bovine genome. Their genetic associations were analyzed using the mixed model with random polygenic effects based on identical-by-state genetic relationships among animals in order to control for spurious associations produced by population structure. Genetic associations of MS were found (P 3.88 x 10(-4)) with six intragenic nucleotide variants on bovine autosomes 3 (cache domain containing 1, CACHD1), 5 (like-glycosyltransferase, LARGE), 16 (cell division cycle 42 binding protein kinase alpha, CDC42BPA) and 21 (snurportin 1, SNUPN; protein tyrosine phosphatase, non-receptor type 9, PTPN9; chondroitin sulfate proteoglycan 4, CSPG4). In particular, the genetic associations with CDC42BPA and LARGE were confirmed using an independent data set of Korean cattle. The results implied that allele frequencies of functional variants and their proximity variants have been augmented by directional selection for greater MS and remain selection signals in the bovine genome. Further studies of fine mapping would be useful to incorporate favorable alleles in marker-assisted selection for MS of Korean cattle.
机译:韩国牛的选择信号可能主要归因于肉质的人工选择。牛基因组中新注释的基因的基因内标记的迅速增加将有助于克服先前研究中选择信号处与肉质相关的遗传标记的有限发现。本研究在韩国牛的选择信号中检验了大理石花纹评分(MS)与基因内核苷酸变异的遗传关联。关联分析使用了407头韩国牛的39 092个核苷酸变异。在牛基因组中新注释的基因中总共选择了129个变体。基于动物之间相同状态的遗传关系,使用具有随机多基因效应的混合模型分析了它们的遗传关联,以控制种群结构产生的虚假关联。发现MS的遗传关联(P <3.88 x 10(-4))与牛常染色体3(缓存域包含1,CACHD1),5(类似糖基转移酶,大),16(细胞分裂周期42)上的六个基因内核苷酸变异结合蛋白激酶α,CDC42BPA)和21(snurportin 1,SNUPN;酪氨酸磷酸酶,非受体9型,PTPN9;硫酸软骨素蛋白聚糖4,CSPG4)。特别是,使用独立的韩国牛数据集证实了与CDC42BPA和LARGE的遗传关联。结果暗示功能性变体及其邻近变体的等位基因频率已经通过定向选择增加了,以获得更大的质谱,并保留了牛基因组中的选择信号。精细定位的进一步研究将有助于将有利的等位基因纳入韩国牛MS的标记辅助选择中。

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