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在菜鸭中与脂质代谢相关基因的克隆与表达

Cloning and expression of the genes associated with lipid metabolism in Tsaiya ducks.

作者信息

Yen C F, Jiang Y N, Shen T F, Wong I M, Chen C C, Chen K C, Chang W C, Tsao Y K, Ding S T

机构信息

Department of Animal Science, National Taiwan University, Taipei, Taiwan.

出版信息

Poult Sci. 2005 Jan;84(1):67-74. doi: 10.1093/ps/84.1.67.

Abstract

Sterol regulatory element binding protein 1 (SREBP1) drives the expression of several lipogenic genes, whereas SREBP2 dictates the expression of every gene involved in cholesterolgenesis in mammals. In the current study, we cloned the cDNA fragments for SREBP1, SREBP2, fatty acid synthase (FAS), 3-hydroxy-3-methylglutaryl-CoA reductase (HMG-CoA reductase), and very low density apolipoprotein-II (apoVLDL-II), the genes associated with lipid metabolism. Fifteen ducks immediately before the first egg was laid (18 wk old) and 15 ducks from the same population at an egg production rate of 80% were killed. Total RNA was extracted from liver and used to amplify the targeted genes by reverse transcription-PCR and screening of a cDNA library. The sequence data showed that Tsaiya duck SREBP1, SREBP2, FAS, and HMG-CoA reductase were highly homologous to that of chicken. Tsaiya duck SREBP1 mRNA was expressed in adipose tissue, cardiac muscle, skeletal muscle, liver, and ovary. The SREBP2 mRNA concentration was highest in liver and ovary. Concentrations of FAS and HMG-CoA reductase mRNA were high in liver and lower in other tissues. The apoVLDL-II mRNA was specifically expressed in the liver. The differences between mRNA concentrations of SREBP1, SREBP2, and FAS in the livers of laying and prelay ducks were not significant. However, the concentrations of hepatic HMG-CoA reductase and apoVLDL-II mRNA were higher in the laying ducks than in prelay ducks. Therefore, laying may affect particular aspects of lipid metabolism, especially biochemical pathways that involved apoVLDL-II and HMG-CoA reductase.

摘要

固醇调节元件结合蛋白1(SREBP1)驱动多种脂肪生成基因的表达,而SREBP2则决定哺乳动物中每个参与胆固醇生成的基因的表达。在本研究中,我们克隆了与脂质代谢相关的基因固醇调节元件结合蛋白1、固醇调节元件结合蛋白2、脂肪酸合酶(FAS)、3-羟基-3-甲基戊二酰辅酶A还原酶(HMG-CoA还原酶)和极低密度载脂蛋白-II(apoVLDL-II)的cDNA片段。选取15只即将产第一枚蛋的鸭(18周龄)和来自同一群体且产蛋率为80%的15只鸭进行宰杀。从肝脏中提取总RNA,并用于通过逆转录PCR和cDNA文库筛选来扩增目标基因。序列数据表明,绿头鸭的SREBP1、SREBP2、FAS和HMG-CoA还原酶与鸡的高度同源。绿头鸭SREBP1 mRNA在脂肪组织、心肌、骨骼肌、肝脏和卵巢中表达。SREBP2 mRNA浓度在肝脏和卵巢中最高。FAS和HMG-CoA还原酶mRNA浓度在肝脏中较高,在其他组织中较低。apoVLDL-II mRNA在肝脏中特异性表达。产蛋鸭和产蛋前鸭肝脏中SREBP1、SREBP2和FAS的mRNA浓度差异不显著。然而,产蛋鸭肝脏中HMG-CoA还原酶和apoVLDL-II mRNA的浓度高于产蛋前鸭。因此,产蛋可能会影响脂质代谢的特定方面,特别是涉及apoVLDL-II和HMG-CoA还原酶的生化途径。

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