首页> 外文期刊>Biochemical and Biophysical Research Communications >Regulation of the promoter region of the human adiponutrin/PNPLA3 gene by glucose and insulin.
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Regulation of the promoter region of the human adiponutrin/PNPLA3 gene by glucose and insulin.

机译:葡萄糖和胰岛素对人脂联蛋白/ PNPLA3基因启动子区域的调节。

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摘要

The adiponutrin/PNPLA3 gene is highly expressed in adipose tissue and liver. Its expression is down-regulated by fasting and rapidly induced by refeeding a high carbohydrate diet. We aimed to determine whether the promoter region of adiponutrin is regulated by glucose and insulin. Endogenous adiponutrin mRNA was increased in mouse 3T3-L1 and human SGBS adipocytes and in human HepG2 cells cultured in 25 mM glucose compared to absence of glucose. A 3100 bp 5'-upstream region of the human adiponutrin gene was cloned into a luciferase reporter plasmid and used in transient transfection studies. Promoter activity was up-regulated by 25 mM glucose, 4.7-fold in HepG2 cells and 2-fold in CHO cells. The effect was shown in CHO cells to be concentration dependent and to depend on glucose metabolism as a non-metabolisable analogue was without effect. In CHO cells constitutively expressing human insulin receptor (CHO-IR), there was a concentration dependent increase of promoter activity by insulin in the presence of glucose. Cotransfection with an expression plasmid for upstream stimulatory factor 2 (USF2), increased promoter activity 1.6-fold in CHO-IR cells. The combined effect of insulin and USF2 (2.3-fold) was greater than the individual effects. Cotransfection of carbohydrate-response element binding protein did not elicit any induction of promoter activity. These results point to potential mechanisms for the observed in vivo nutritional regulation of adiponutrin expression and its up-regulation in fatty liver and by obesity.
机译:脂联蛋白/ PNPLA3基因在脂肪组织和肝脏中高表达。它的表达由于禁食而下调,而通过补充高糖饮食迅速诱导。我们旨在确定脂联素的启动子区域是否受葡萄糖和胰岛素的调节。与不存在葡萄糖的情况相比,在25 mM葡萄糖中培养的小鼠3T3-L1和人SGBS脂肪细胞以及人HepG2细胞中,内源性脂联素mRNA增加。将人脂联蛋白基因的3100 bp 5'-上游区域克隆到荧光素酶报告质粒中,并用于瞬时转染研究。启动子活性由25 mM葡萄糖上调,在HepG2细胞中是4.7倍,在CHO细胞中是2倍。由于不可代谢的类似物没有作用,因此在CHO细胞中显示该作用是浓度依赖性的并且依赖于葡萄糖代谢。在组成型表达人胰岛素受体(CHO-IR)的CHO细胞中,胰岛素在葡萄糖存在下具有浓度依赖性的启动子活性增加。共表达与上游刺激因子2(USF2)的表达质粒,在CHO-IR细胞中启动子活性提高了1.6倍。胰岛素和USF2的联合作用(2.3倍)大于单个作用。碳水化合物反应元件结合蛋白的共转染未引起启动子活性的任何诱导。这些结果指出了观察到的脂联蛋白的体内营养调节及其在脂肪肝和肥胖中的上调的潜在机制。

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