Lefevre P, Tripon E, Plumelet C, Douaire M, Diot C
Unité Mixte de Recherche INRA-ENSA de Génétique Animale, 65 rue de Saint-Brieuc, 35042 Rennes cedex, France.
Biochem Biophys Res Commun. 2001 Jan 12;280(1):25-31. doi: 10.1006/bbrc.2000.4070.
In chicken, adiposity is influenced by hepatic stearoyl-CoA desaturase (SCD) 1. This gene is up-regulated by low-fat high-carbohydrate diet and down-regulated by addition of polyunsaturated fatty acids (PUFA). In this study, we present evidence for an inhibition of chicken SCD1 expression by PUFA using reporter gene constructs in transient transfection assays. This inhibition does not involve the peroxisome proliferator-activated receptor pathway, in contrast with what has been observed in rodents. We were able to localise a PUFA as well as an insulin response element within the -372/+125 bp region of the promoter. Sequence analyses of this region allowed identification of several cis-regulatory elements: A sterol regulatory element (SRE) and a juxtaposed NF-Y element which have been shown to be involved in the regulation of mouse SCD genes by PUFA. In addition, we identified an overlapping Sp1/USF motif, which was described to play a role in insulin/glucose and PUFA regulation of fatty synthase, ATP-citrate-lyase, and leptin genes. These data provide the first characterisation of the chicken SCD1 promoter and putative cis-sequences involved in the regulation of this gene by PUFA and insulin.
在鸡中,肥胖受肝脏硬脂酰辅酶A去饱和酶(SCD)1的影响。该基因在低脂高碳水化合物饮食条件下上调,而在添加多不饱和脂肪酸(PUFA)时下调。在本研究中,我们通过瞬时转染实验中的报告基因构建体,提供了PUFA抑制鸡SCD1表达的证据。与在啮齿动物中观察到的情况相反,这种抑制不涉及过氧化物酶体增殖物激活受体途径。我们能够在启动子的-372 / +125 bp区域内定位一个PUFA以及一个胰岛素反应元件。对该区域的序列分析允许鉴定几个顺式调节元件:一个固醇调节元件(SRE)和一个并列的NF-Y元件,它们已被证明参与PUFA对小鼠SCD基因的调节。此外,我们鉴定出一个重叠的Sp1 / USF基序,该基序被描述在脂肪酸合酶、ATP-柠檬酸裂解酶和瘦素基因的胰岛素/葡萄糖和PUFA调节中起作用。这些数据首次表征了鸡SCD1启动子以及参与PUFA和胰岛素对该基因调节的假定顺式序列。