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首页> 外文期刊>Molecular and Cellular Probes: The Location, Diagnosis and Monitoring of Disease by Specific Molecules and Cell Lines >Sequence analysis and genetic variability of stearoyl CoA desaturase (SCD) gene in the Italian Mediterranean river buffalo.
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Sequence analysis and genetic variability of stearoyl CoA desaturase (SCD) gene in the Italian Mediterranean river buffalo.

机译:意大利地中海水牛中硬脂酰CoA去饱和酶(SCD)基因的序列分析和遗传变异性。

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摘要

Stearoyl-CoA desaturase (SCD) plays a key metabolic role by changing the saturated FA content of ruminant milk and meat. In this study we characterized for the first time the stearoyl-CoA desaturase (SCD) gene in river buffalo (Bubalus bubalis) and investigated its genetic variability. On a total of 78 buffaloes, 15 SNPs were detected and 6 of them were preliminarily genotyped. In particular, the g.133A>C SNP was found to create a new consensus site for the SP1 binding site, thus generating a new tandem repeat in the promoter region. A preliminary association study with the milk fatty acid content showed that the C allele significantly affects the total desaturation index (P<0.01). Linkage disequilibrium analysis allowed identification of 7 haplotypes and 4 tag SNPs. Such polymorphisms could represent useful genetic markers for association studies with fatty acid composition, but further studies are needed to evaluate their potential use to improve the nutritional quality of the dairy products.
机译:硬脂酰辅酶A去饱和酶(SCD)通过改变反刍动物牛奶和肉类的饱和FA含量发挥关键的代谢作用。在这项研究中,我们首次表征了水牛(Bubalus bubalis)中的硬脂酰辅酶A去饱和酶(SCD)基因,并研究了其遗传变异性。在总共78个水牛中,检测到15个SNP,并对其中的6个进行了初步基因分型。特别是,发现g.133A> C SNP为SP1结合位点创建了一个新的共有位点,从而在启动子区域产生了一个新的串联重复序列。与牛奶脂肪酸含量的初步关联研究表明,C等位基因显着影响总去饱和指数(P <0.01)。连锁不平衡分析允许鉴定7个单倍型和4个标签SNP。这种多态性可以代表有用的遗传标记,用于脂肪酸组成的关联研究,但是需要进一步的研究来评估其潜在用途,以改善乳制品的营养质量。

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