Jiang Zhihua, Michal Jennifer J, Tobey David J, Wang Zeping, Macneil Michael D, Magnuson Nancy S
Department of Animal Sciences, Washington State University, Pullman, WA 99164-6351, USA.
Int J Biol Sci. 2008 Apr 23;4(2):96-102. doi: 10.7150/ijbs.4.96.
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 F(1 )bulls, 113 F(1 )dams and ~250 F(2 )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, Delta(9) 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.
多项报告显示,尾加压素2(UTS2)及其受体(UTS2R)参与葡萄糖代谢和胰岛素抵抗,而这会导致人类2型糖尿病(T2DM)的发生。在本研究中,我们注释了牛的UTS2和UTS2R基因,并在前一个基因中鉴定出5个单核苷酸多态性(SNP),在后一个基因中鉴定出14个突变。在一个和牛×利木赞参考群体中对4个突变进行了基因分型,该群体包括6头F1公牛、113头F1母牛和大约250头F2后代。在与脂肪沉积和脂肪酸组成相关的12种表型中,我们观察到UTS2基因与骨骼饱和脂肪酸的含量显著相关,而其受体(UTS2R)基因对饱和脂肪酸和单不饱和脂肪酸的含量、将16:0转化为16:1的Δ9去饱和酶活性、肌肉脂肪(大理石花纹)评分和背最长肌面积有显著影响。然而,在这个群体中,这些标记与皮下脂肪深度或肾、盆腔和心脏脂肪百分比无关。我们还发现,启动子区域的突变改变了两个基因的启动子活性,编码SNP可能影响UTS2R基因中的mRNA稳定性。总体而言,我们目前的研究首次提供了证据,表明UTS2和UTS2R基因都调节骨骼肌脂肪积累和脂肪酸代谢,从而表明它们在人类中与肥胖和T2DM相关的潜在病理功能。