Department of Animal Genetics and Breeding, College of Veterinary and Animal Sciences, Kerala Veterinary and Animal Sciences University, Thrissur, Kerala, India.
Base Farm, Kolahalamedu, Kerala Veterinary and Animal Sciences University, Idukki, Kerala, India.
Anim Biotechnol. 2023 Dec;34(8):3837-3846. doi: 10.1080/10495398.2023.2232662. Epub 2023 Jul 10.
We analyzed the effect of a single nucleotide polymorphism, g. C3141T in the 3' UTR of Signal transducer and activator of transcription-1 gene () on milk production traits in the Holstein Friesian crossbred cattle of Kerala (n = 144) by association analysis and expression study. The population was genotyped by restriction fragment length polymorphism using 1. Association study using the General Linear Model-Analysis of Variance revealed that none of the yield or composition traits analyzed were significantly differed. The expression profile of gene in leucocytes of animals bearing homozygous genotypes was compared by quantitative real time PCR using SYBR green chemistry with and relative expression was not found to be significantly differed. The second stage of the study, the mRNA spanning 3213 bp was amplified from leucocytes and sequenced (GenBank: MT459802.1). Two novel SNPs were identified; one synonymous mutation in the coding region (g.A1212G) and the other in the 3'UTR (g.T3042C). The novel SNPs might contribute to gene regulation mediated by alternate spicing or binding sites for regulatory molecules. The results reiterate the importance of extensive studies of gene variants to substantiate the presence of a quantitative trait loci for dairy traits in the vicinity of gene.
我们通过关联分析和表达研究分析了信号转导和转录激活因子 1 基因()3'UTR 中的单核苷酸多态性 g.C3141T 对喀拉拉邦荷斯坦弗里森杂交牛(n=144)产奶性状的影响。通过限制性片段长度多态性,使用 1 对群体进行基因分型。一般线性模型方差分析的关联研究显示,分析的产奶量或成分性状均无显著差异。通过 SYBR 绿色化学定量实时 PCR 比较了具有纯合基因型的动物白细胞中基因的表达谱,相对表达量未发现有显著差异。研究的第二阶段,从白细胞中扩增了跨越 3213bp 的 mRNA 并进行测序(GenBank:MT459802.1)。鉴定出两个新的 SNPs;一个是编码区的同义突变(g.A1212G),另一个是 3'UTR 中的突变(g.T3042C)。这些新的 SNP 可能有助于通过可变剪接或调节分子结合位点来调节基因表达。研究结果再次强调了对基因变异进行广泛研究的重要性,以证实 基因附近存在与奶牛性状相关的数量性状基因座。