Zhang Yue, Zhang Min, Su Hong, Liu Jun, Zhao Feifei, Zhao Yifan, Li Xiunan, Yang Yanyan, Cao Guifang, Zhang Yong
College of Veterinary Medicine, Northwest A&F University, Yangling 712100, China.
College of Veterinary Medicine, Inner Mongolia Agricultural University, Hohhot 010018, China.
Animals (Basel). 2025 Aug 5;15(15):2284. doi: 10.3390/ani15152284.
Ujimqin sheep, known for its distinctive multi-vertebrae phenotypes (T13L7, T14L6, and T14L7) and economic value, has garnered significant attention. However, conventional phenotypic detection methods suffer from low efficiency and high costs. In this study, based on a key SNP locus ( gene, Chr7:89393414, C > T) identified through a genome-wide association study (GWAS), a TaqMan-MGB (minor groove binder) genotyping system was developed. the objective was to establish a high-throughput and efficient molecular marker-assisted selection (MAS) tool. Specific primers and dual fluorescent probes were designed to optimize the reaction system. Standard plasmids were adopted to validate genotyping accuracy. A total of 152 Ujimqin sheep were subjected to TaqMan-MGB genotyping, digital radiography (DR) imaging, and Sanger sequencing. the results showed complete concordance between TaqMan-MGB and Sanger sequencing, with an overall agreement rate of 83.6% with DR imaging. For individuals with T/T genotypes (127/139), the detection accuracy reached 91.4%. This method demonstrated high specificity, simplicity, and cost-efficiency, significantly reducing the time and financial burden associated with traditional imaging-based approaches. the findings indicate that the TaqMan-MGB technique can accurately identify the T/T genotype at the SNP site and its strong association with the multi-vertebrae phenotypes, offering an effective and reliable tool for molecular breeding of Ujimqin sheep.
乌珠穆沁羊以其独特的多脊椎表型(T13L7、T14L6和T14L7)和经济价值而闻名,备受关注。然而,传统的表型检测方法效率低、成本高。在本研究中,基于通过全基因组关联研究(GWAS)确定的一个关键SNP位点(基因,Chr7:89393414,C>T),开发了一种TaqMan-MGB(小沟结合剂)基因分型系统。目的是建立一种高通量、高效的分子标记辅助选择(MAS)工具。设计了特异性引物和双荧光探针以优化反应体系。采用标准质粒验证基因分型准确性。对152只乌珠穆沁羊进行了TaqMan-MGB基因分型、数字X线摄影(DR)成像和桑格测序。结果显示,TaqMan-MGB与桑格测序结果完全一致,与DR成像的总体一致率为83.6%。对于T/T基因型个体(127/139),检测准确率达到91.4%。该方法具有高特异性、简便性和成本效益,显著减少了与传统基于成像的方法相关的时间和经济负担。研究结果表明,TaqMan-MGB技术能够准确鉴定SNP位点的T/T基因型及其与多脊椎表型的强相关性,为乌珠穆沁羊的分子育种提供了一种有效且可靠的工具。