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首页> 外文期刊>Animal Science Papers and Reports >Nucleotide sequence polymorphisms in the promoter region of bovine growth hormone receptor gene (GHR) have no effect on its expression level in liver
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Nucleotide sequence polymorphisms in the promoter region of bovine growth hormone receptor gene (GHR) have no effect on its expression level in liver

机译:牛生长激素受体基因(GHR)启动子区域的核苷酸序列多态性对其在肝脏中的表达水平没有影响

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摘要

The gene coding for bovine GHR consists of nine protein-coding exons and untranslated, alternative exons 1A, 1B, and 1C in its 5'-region. Distinct promoters regulate transcription from each of the alternative exons. The P1 promoter which drives growth hormone receptor expression in the liver is associated with exon 1A. Earlier the nucleotide sequence polymorphisms have been identified in the bovine GHR gene promoter region, including several single nucleotide polymorphisms (SNPs) and one TG repeat (microsatellite) of variable length. Using computer-aided analysis in TESS programme it has also been shown that the A/G transition at position -154 (PFLP-NsiI) and the C/T transition at position -1104 (Fnu4HI), both located upstream the exon 1A, co-localized with putative transcription factor-binding sites. In light of this the authors decided to study possible effects of these polymorphisms on GHR gene expression in cattle of different GHR genotypes, using Real-time PCR. Interestingly, no difference was found in GHR mRNA accumulation in liver between young Black-and-White (BW) bulls carrying (+/+), (+/-) or (-/-) genotypes at RFLP-NsiI site, (+/-) or (+/+) genotypes at RFLP-Fnu4HI site, and TG(17/17) or TG(21/21) alleles at TG(n) microsatellite, located within the P1 promoter of the bovine GHR gene.
机译:编码牛GHR的基因在其5'区域由9个蛋白质编码外显子和未翻译的替代外显子1A,1B和1C组成。不同的启动子调节每个替代外显子的转录。在肝脏中驱动生长激素受体表达的P1启动子与外显子1A相关。早先已在牛GHR基因启动子区域鉴定出核苷酸序列多态性,包括几种单核苷酸多态性(SNP)和一个长度可变的TG重复序列(微卫星)。使用TESS程序中的计算机辅助分析,还显示了位置-154的A / G跃迁(PFLP-NsiI)和位置-1104的C / T跃迁(Fnu4HI),均位于外显子1A,co -定位于假定的转录因子结合位点。有鉴于此,作者决定使用实时PCR研究这些多态性对不同GHR基因型牛的GHR基因表达的可能影响。有趣的是,在RFLP-NsiI位点上携带(+ / +),(+/-)或(-/-)基因型的年轻黑白(BW)公牛之间,肝脏GHR mRNA的积累没有差异,(+ /-)或RFLP-Fnu4HI位点的(+ / +)基因型,以及位于牛GHR基因P1启动子内的TG(n)微卫星上的TG(17/17)或TG(21/21)等位基因。

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