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首页> 外文期刊>Journal of genetics >Sequence variants of the LCORL gene and its association with growth and carcass traits in Qinchuan cattle in China
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Sequence variants of the LCORL gene and its association with growth and carcass traits in Qinchuan cattle in China

机译:LCORL基因的序列变体及其与中国秦川牛生长和胴体性状的关系

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Molecular marker-assisted selection is a better way to satisfy the growing customer requirement with the development of beef cattle growth and breeding research. For now, quantitative trait locus (QTL) for cattle growth and carcass traits, just like body height, body length and carcass weight have been detected on bovine chromosome 6. In this study, ligand-dependent nuclear receptor corepressor-like (LCORL) was selected as the potential positional candidate gene located in chromosome 6 which is closely connected with the bovine growth and carcass traits. A total of 450 Qinchuan beef cattle were used to detect mutations in exon and its neighbouring region, and the promoter region of the bovine LCORL gene. The methods for SNPs detection were polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) and created restriction site PCR (CRS-PCR), and the results of this study show that there were two variations in intron regions, the other four variations were located in the promoter region. Linkage disequilibrium analysis and haplotype analysis indicated that L78-Q4 had strong linkage disequilibrium, A T G C G C (16.2%) and G C G C A T (16.7%) had higher haplotype frequencies, G C A C A C (0.8%) and G T A C A T (0.7%) had lower haplotype frequencies. Correlation analysis indicated that SNP g. INT + 52098A > G was significantly associated with slaughter weight and carcass weight. Based on the research, we selected LCORL as the candidate gene that can contribute to improved marker-assisted selection for the meat performance of Qinchuan beef cattle.
机译:分子标记辅助选择是一种更好的方式,以满足牛肉生长和育种研究的发展日益增长的客户需求。目前,在牛染色体6中检测到牛生长和胴体性状的定量特质基因座(QTL),就像身体高度一样,体长和胴体重量。在本研究中,依赖于依赖于依赖于配体的核受体铁芯压(LCORL)是选择作为位于染色体6中的潜在位置候选基因,其与牛生长和胎体性状密切相关。共使用450个Qinchuan牛肉牛来检测外显子及其相邻区域的突变,以及牛LCORL基因的启动子区。 SNPS检测方法是聚合酶链反应限制片段长度多态性(PCR-RFLP)和产生的限制性位点PCR(CRS-PCR),并且本研究结果表明,内含子区域有两种变化,其他四种变化位于启动子地区。联动不平衡分析和单倍型分析表明,L78-Q4具有强烈的连锁不平衡,A T G C G C(16.2%)和G C G C A T(16.7%)具有更高的单倍型频率,G C A C(0.8%)和G T A C A T(0.7%)具有较低的单倍型频率。相关分析表明SNP G.嵌段+ 52098A> G与屠宰重量和胴体重量显着相关。基于研究,我们选择了LCORL作为候选基因,可以有助于改善秦川牛肉牛肉性能的改进的标志辅助选择。

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