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Comparative understanding of UTS2 and UTS2R genes for their involvement in type 2 diabetes mellitus

机译:对UTS2和UTS2R基因参与2型糖尿病的比较理解

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Several reports have shown that urotensin 2 (UTS2) and its receptor (UTS2R) are involved in glucose metabolism and insulin resistance, which lead to development of type 2 diabetes mellitus (T2DM) in humans. In the present study, we annotated both bovine UTS2 and UTS2R genes and identified 5 single nucleotide polymorphisms (SNPs) for the former gene and 14 mutations for the latter gene. Four mutations were genotyped on a Wagyu x Limousin reference population, including 6 F1 bulls, 113 F1 dams and ~250 F2 progeny. Among 12 phenotypes related to fat deposition and fatty acid composition, we observed that the UTS2 gene was significantly associated with the amount of skeletal saturated fatty acids, while its receptor (UTS2R) gene had significant effects on amounts of saturated and monounsaturated fatty acids, Δ9 desaturase activity for converting 16:0 into 16:1, muscle fat (marbling) score and Longissimus Dorsi muscle area. However, in this population, these markers were not associated with subcutaneous fat depth or percent kidney, pelvic and heart fat. We also found that mutations in the promoter regions altered the promoter activities in both genes and coding SNPs might affect the mRNA stability in the UTS2R gene. Overall, our present study provides the first evidence that both UTS2 and UTS2R genes regulate skeletal muscle fat accumulation and fatty acid metabolism, thus indicating their potential pathological functions related to obesity and T2DM in humans.
机译:几篇报道表明,尿素2(UTS2)及其受体(UTS2R)参与葡萄糖代谢和胰岛素抵抗,从而导致人类2型糖尿病(T2DM)的发展。在本研究中,我们对牛UTS2和UTS2R基因进行了注释,并确定了前者基因的5个单核苷酸多态性(SNP)和后者基因的14个突变。在Wagyu x Limousin参考种群上对四个突变进行了基因分型,包括6个F1公牛,113个F1大坝和〜250 F2后代。在与脂肪沉积和脂肪酸组成有关的12个表型中,我们观察到UTS2基因与骨骼饱和脂肪酸的量显着相关,而其受体(UTS2R)基因对饱和和单不饱和脂肪酸的量Δ9有显着影响。将16:0转换为16:1的去饱和酶活性,肌肉脂肪(大理石花纹)得分和背最长肌肌肉区域。但是,在这些人群中,这些标志物与皮下脂肪深度或肾脏,骨盆和心脏脂肪百分比无关。我们还发现,启动子区域中的突变改变了两个基因中的启动子活性,编码SNP可能会影响UTS2R基因中的mRNA稳定性。总体而言,我们的研究提供了第一个证据,即UTS2和UTS2R基因均调节骨骼肌脂肪积累和脂肪酸代谢,从而表明它们与人类肥胖和T2DM相关的潜在病理功能。

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