Tao Meini, Li Zhiqiang, Liu Meng, Ma Haiyu, Liu Wujun
College of Animal Science, Xinjiang Agricultural University, Urumqi, China.
Adsen Biotechnology Co., Ltd., Urumchi, China.
Front Genet. 2024 Apr 12;15:1371872. doi: 10.3389/fgene.2024.1371872. eCollection 2024.
The aim was to investigate the relationship between polymorphisms of gene mutation loci and reproductive traits in local sheep breeds (Duolang Sheep) and introduced sheep breeds (Suffolk, Hu Sheep) in Xinjiang to provide new molecular markers for the selection and breeding of high fecundity sheep. The expression pattern of typing successful genes in sheep tissues was investigated by RT-qPCR technology, providing primary data for subsequent verification of gene function. The 26 mutation loci of , , , , and genes were typed using KASP. Association analyses were performed using SPSS 25.0, and the typing results showed that five genes with six loci, (g.14962207 C>T), (g.48271079 C>A), (g.27107842 T>C, g.27108855 G>A), (g.86134602 G>A), and (g.80789180 T>G) were successfully typed. The results of the association analyses showed that (g.14962207 C>T), (g.27108855 G>A), (g.48271079 C>A), and (g.80789180 T>G) caused significant or extremely significant effects on the litter size in Duolang, Suffolk and Hu Sheep populations. The expression distribution pattern of the five genes in 12 sheep reproduction-related tissues was examined by RT-qPCR. The results showed that the expression of the gene in the uterus, the gene in the ovary, and the gene in hypothalamic-pituitary-gonadal axis-related tissues were significantly higher than in the tissues of other parts of the sheep. and genes were highly expressed both in reproductive organs and visceral tissues. In summary, the (g.14962207 C>T), (g.27108855 G>A), (g.48271079 C>A), and (g.80789180 T>G) loci can be used as potential molecular markers for detecting differences in reproductive performance in sheep. Due to variations in typing results, the (g.27107842 T>C) and (g.86134602 G>A) loci need further validation.
目的是研究新疆本地绵羊品种(多浪羊)以及引进绵羊品种(萨福克羊、湖羊)基因突变位点多态性与繁殖性状之间的关系,为高繁殖力绵羊的选育提供新的分子标记。采用RT-qPCR技术研究绵羊组织中分型成功基因的表达模式,为后续基因功能验证提供基础数据。利用KASP对、、、、和基因的26个突变位点进行分型。使用SPSS 25.0进行关联分析,分型结果显示成功分型了6个位点的5个基因,即(g.14962207 C>T)、(g.48271079 C>A)、(g.27107842 T>C、g.27108855 G>A)、(g.86134602 G>A)和(g.80789180 T>G)。关联分析结果表明,(g.14962207 C>T)、(g.27108855 G>A)、(g.48271079 C>A)和(g.80789180 T>G)对多浪羊、萨福克羊和湖羊群体的产羔数有显著或极显著影响。采用RT-qPCR检测这5个基因在12种绵羊繁殖相关组织中的表达分布模式。结果表明,基因在子宫中的表达、基因在卵巢中的表达以及基因在下丘脑-垂体-性腺轴相关组织中的表达均显著高于绵羊其他部位的组织。和基因在生殖器官和内脏组织中均高表达。综上所述,(g.14962207 C>T)、(g.27108855 G>A)、(g.48271079 C>A)和(g.80789180 T>G)位点可作为检测绵羊繁殖性能差异的潜在分子标记。由于分型结果存在差异,(g.27107842 T>C)和(g.86134602 G>A)位点需要进一步验证。