Ishimoto Kenji, Nakamura Hiroki, Tachibana Keisuke, Yamasaki Daisuke, Ota Akemi, Hirano Ken-Ichi, Tanaka Toshiya, Hamakubo Takao, Sakai Juro, Kodama Tatsuhiko, Doi Takefumi
Graduate School of Pharmaceutical Sciences, Osaka University, 1-6 Yamadaoka, Suita, Osaka 565-0871; Department of Molecular Pharmaceutical Science, Graduate School of Medicine, Osaka University, Suita, Osaka 565-0871.
Graduate School of Pharmaceutical Sciences, Osaka University, 1-6 Yamadaoka, Suita, Osaka 565-0871.
J Biol Chem. 2009 Aug 14;284(33):22195-22205. doi: 10.1074/jbc.M109.028753. Epub 2009 Jun 24.
Lipin 1 plays a crucial role in lipid metabolism in adipose tissue, skeletal muscle, and liver. Its physiological role involves two cellular functions: regulation of phosphatidate phosphatase activity and regulation of fatty acid oxidation. In this study, we have demonstrated that lipin 1 gene (LPIN1) expression is regulated by cellular sterols, which are key regulators of lipid metabolism. We have also characterized the sterol-response element and nuclear factor Y-binding sites in the human LPIN1 promoter. Using a luciferase assay, electrophoretic mobility shift assay, and chromatin immunoprecipitation assay, we demonstrated that these elements are responsible for the transcription of LPIN1 gene, mediated by SREBP-1 (sterol regulatory element-binding protein 1) and nuclear factor Y. Furthermore, we investigated whether lipin 1 is involved in lipogenesis by transfection of LPIN1 small interfering RNA. We infer that sterol-mediated regulation of lipin 1 gene transcription modulates triglyceride accumulation. This modulation involves changes in the activity of phosphatidate phosphatase.
脂联素1在脂肪组织、骨骼肌和肝脏的脂质代谢中起关键作用。其生理作用涉及两种细胞功能:调节磷脂酸磷酸酶活性和调节脂肪酸氧化。在本研究中,我们证明了脂联素1基因(LPIN1)的表达受细胞固醇调节,而细胞固醇是脂质代谢的关键调节因子。我们还对人LPIN1启动子中的固醇反应元件和核因子Y结合位点进行了表征。使用荧光素酶测定、电泳迁移率变动分析和染色质免疫沉淀分析,我们证明这些元件负责由固醇调节元件结合蛋白1(SREBP-1)和核因子Y介导的LPIN1基因转录。此外,我们通过转染LPIN1小干扰RNA研究了脂联素1是否参与脂肪生成。我们推断固醇介导的脂联素1基因转录调节可调节甘油三酯积累。这种调节涉及磷脂酸磷酸酶活性的变化。