Kumadaki Shin, Matsuzaka Takashi, Kato Toyonori, Yahagi Naoya, Yamamoto Takashi, Okada Sumiyo, Kobayashi Kazuto, Takahashi Akimitsu, Yatoh Shigeru, Suzuki Hiroaki, Yamada Nobuhiro, Shimano Hitoshi
Department of Internal Medicine (Endocrinology and Metabolism), Graduate School of Comprehensive Human Sciences, University of Tsukuda, 1-1-1 Tennodai, Tsukuba, Ibaraki 305-8575, Japan.
Biochem Biophys Res Commun. 2008 Apr 4;368(2):261-6. doi: 10.1016/j.bbrc.2008.01.075. Epub 2008 Jan 28.
Elovl-6, a long fatty acid elongase, contributes to de novo synthesis of fatty acids and regulates hepatic insulin sensitivity. Hepatic regulation of Elovl-6 gene expression in various nutritional conditions suggested that, like other lipogenic enzyme genes, Elovl-6 is a target of SREBP-1, a transcription factor governing fatty acid synthesis. Supportively, adenoviral RNAi knockdown of SREBP-1 in mouse liver suppressed Elovl-6 mRNA and fatty acid synthase levels. Therefore, we analyzed mouse Elovl-6 gene promoter to determine its role as an SREBP-1 target. Luciferase reporter assays of 1.4-kb 5' flanking region of mouse Elovl-6 gene in HepG2 cells demonstrated that nuclear SREBPs activated the Elovl-6 promoter, highlighting two SREBP binding sites: proximal SRE-1 and distal SRE-2. EMSA indicated that SRE-1 had higher affinity than SRE-2 for SREBP. ChIP assays confirmed in vivo binding of hepatic nuclear SREBP-1c protein. These data demonstrated that Elovl-6 is regulated directly and primarily by SREBP-1c.
ELOVL-6是一种长链脂肪酸延长酶,参与脂肪酸的从头合成并调节肝脏胰岛素敏感性。在不同营养条件下肝脏对ELOVL-6基因表达的调控表明,与其他生脂酶基因一样,ELOVL-6是SREBP-1的靶标,SREBP-1是一种控制脂肪酸合成的转录因子。支持这一观点的是,腺病毒RNA干扰敲低小鼠肝脏中的SREBP-1可抑制ELOVL-6 mRNA和脂肪酸合酶水平。因此,我们分析了小鼠ELOVL-6基因启动子,以确定其作为SREBP-1靶标的作用。在HepG2细胞中对小鼠ELOVL-6基因1.4 kb 5'侧翼区域进行荧光素酶报告基因检测表明,核SREBPs激活了ELOVL-6启动子,突出显示了两个SREBP结合位点:近端SRE-1和远端SRE-2。电泳迁移率变动分析表明,SRE-1对SREBP的亲和力高于SRE-2。染色质免疫沉淀分析证实了肝脏核SREBP-1c蛋白在体内的结合。这些数据表明,ELOVL-6直接且主要受SREBP-1c调控。