College of Animal Science and Technology, Northwest A&F University, Yangling, P.R. China.
Faculty of Veterinary and Livestock Technology, S. Seifullin Kazakh Agro technical University, Nur-Sultan, Kazakhstan.
Anim Biotechnol. 2023 Nov;34(6):1950-1959. doi: 10.1080/10495398.2022.2059667. Epub 2022 Apr 21.
The () gene regulates adipogenesis and myogensis. In this study, sequencing of prompter region identified three SNPs at loci g.78G > A, g.116C > T and g.201A > T. Each SNP yields three genotypes as GG, GA and AA at loci g.78G > A, CC, CT and TT at loci g.116C > T and AA, AT and TT at loci g.201A > T. Allelic and genotypic frequencies of all three SNPs deviated from the Hardy-Weinberg equilibrium (HWE) ( < 0.05) and were found highly polymorphic as PIC (0.25 < PIC < 0.50). Moreover, we found highest LD (D'/γ2) between SNP2 and SNP3 (0.989/0.909), followed by SNP1 and SNP3 (0.944/0.796). Moreover, three variants of FGF10 gene promoter exhibited significant (P < 0.05) association with body measurement and carcass quality traits in Qinchuan beef cattle. At loci g.78G > A, the genotype GG showed significantly (P < 0.01) larger body length (BL), rump length (RL), chest depth (CD), chest circumference (CC) and ultrasound loin area (ULA). The genotype TC at loci g.116C > T showed significantly ( < 0.01 and 0.05) larger body measurement and intramuscular fat, and ultrasound loin area (ULA). In addition to that, at loci g.201A > T, genotype TT showed significantly (P < 0.01 and P < 0.05) larger body length (BL), rump length (RL), hip width (HW), chest circumference (CC) and ultrasound loin area (ULA). Additionally, screening of promoter sequence of gene explored loss of four TFs binding sites (, , and ) at g.116C > T because of SNP2. However, a single TF binding site was lost at g.202A > T due to SNP3. Interestingly, none of TF binding site was lost at g.78G > A in SNP1; however, one new TF binding site was gained at this location due to SNP1. These findings conclude that genotype GG, TC and TT could be used as genetic markers of gene for body measurement and carcass quality traits in Qinchuan beef cattle.
基因调控脂肪生成和肌生成。在这项研究中,对启动子区域进行测序,在 g.78G > A、g.116C > T 和 g.201A > T 三个基因座鉴定到三个 SNP。每个 SNP 在 g.78G > A 基因座产生三种基因型 GG、GA 和 AA,在 g.116C > T 基因座产生 CC、CT 和 TT,在 g.201A > T 基因座产生 AA、AT 和 TT。所有三个 SNP 的等位基因和基因型频率均偏离 Hardy-Weinberg 平衡(HWE)(P < 0.05),且表现出高度多态性,PIC(0.25 < PIC < 0.50)。此外,我们发现 SNP2 和 SNP3 之间的 LD 最高(D'/γ2)(0.989/0.909),其次是 SNP1 和 SNP3(0.944/0.796)。此外,三个 FGF10 基因启动子变体与秦川肉牛的体尺和胴体质量性状显著相关(P < 0.05)。在 g.78G > A 基因座上,基因型 GG 显著(P < 0.01)表现出更大的体尺(BL)、臀部长度(RL)、胸深(CD)、胸围(CC)和超声腰面积(ULA)。g.116C > T 基因座上的 TC 基因型表现出更大的体尺和肌内脂肪以及超声腰面积(ULA)(P < 0.01 和 0.05)。此外,g.201A > T 基因座上,TT 基因型显著(P < 0.01 和 P < 0.05)表现出更大的体长(BL)、臀部长度(RL)、髋宽(HW)、胸围(CC)和超声腰面积(ULA)。此外,通过对基因启动子序列进行筛选,发现 SNP2 导致 g.116C > T 时失去了四个 TF 结合位点(、、和),而 SNP3 导致 g.202A > T 时失去了一个 TF 结合位点。有趣的是,SNP1 中没有 TF 结合位点丢失在 g.78G > A,但由于 SNP1,在该位置获得了一个新的 TF 结合位点。这些发现表明,基因型 GG、TC 和 TT 可作为秦川肉牛体尺和胴体质量性状的遗传标记。