Han Y J, Chen Y, Liu Y, Liu X L
College of Animal Science and Technology, Northwest A&F University, No. 22, Xinong Road, Yangling, Shaanxi 712100, People's Republic of China.
J Genet. 2017 Mar;96(1):9-17. doi: 10.1007/s12041-016-0732-0.
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 (CRSPCR), 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.
随着肉牛生长和育种研究的发展,分子标记辅助选择是满足不断增长的客户需求的更好方法。目前,已经在牛的6号染色体上检测到与牛生长和胴体性状相关的数量性状位点(QTL),如体高、体长和胴体重。在本研究中,配体依赖性核受体共抑制因子样(LCORL)被选为位于6号染色体上的潜在位置候选基因,它与牛的生长和胴体性状密切相关。总共450头秦川肉牛被用于检测外显子及其相邻区域以及牛LCORL基因启动子区域的突变。单核苷酸多态性(SNP)检测方法为聚合酶链反应-限制性片段长度多态性(PCR-RFLP)和创造酶切位点PCR(CRSPCR),本研究结果表明内含子区域有两个变异,另外四个变异位于启动子区域。连锁不平衡分析和单倍型分析表明,L78-Q4有很强的连锁不平衡,ATGCGC(16.2%)和GCGCAT(16.7%)有较高的单倍型频率,GCACAC(0.8%)和GTACAT(0.7%)有较低的单倍型频率。相关性分析表明,SNP g.INT+52098A>G与屠宰体重和胴体重显著相关。基于该研究,我们选择LCORL作为候选基因,它有助于改进秦川肉牛产肉性能的标记辅助选择。