Graduate School of Pharmaceutical Sciences, Osaka University, 1-6 Yamadaoka, Suita, Osaka 565-0871, Japan.
Biochem J. 2010 Jul 15;429(2):347-57. doi: 10.1042/BJ20091511.
FDPS (farnesyl diphosphate synthase) catalyses the formation of farnesyl diphosphate, a key intermediate in the synthesis of cholesterol and isoprenylated cellular metabolites. FDPS is also the molecular target of nitrogen-containing bisphosphonates, which are used as bone-antiresorptive drugs in various disorders. In the present study, we characterized the sterol-response element and NF-Y (nuclear factor Y)-binding site in the human FDPS promoter. Using a luciferase assay, electrophoretic mobility-shift assay and chromatin immunoprecipitation assay, we demonstrated that these elements are responsible for the transcription of the FDPS gene, and that its transcriptional activation is mediated by SREBP-2 (sterol-regulatory-element-binding protein 2) and NF-Y. We also investigated whether sterol-mediated FDPS expression is involved in the cell proliferation induced by zoledronic acid, an FDPS inhibitor. We show that the SREBP-2- and NF-Y-mediated regulation of FDPS gene transcription modulates cell proliferation. These results suggest that SREBP-2 and NF-Y are required to trigger cell proliferation through the induction of FDPS expression and that the pharmacological action of zoledronic acid is involved in this pathway.
FDPS(法呢基二磷酸合酶)催化法呢基二磷酸的形成,这是胆固醇和异戊烯基化细胞代谢物合成的关键中间产物。FDPS 也是含氮双膦酸盐的分子靶标,含氮双膦酸盐被用作各种疾病的抗骨质吸收药物。在本研究中,我们对人 FDPS 启动子中的固醇反应元件和 NF-Y(核因子 Y)结合位点进行了表征。通过荧光素酶测定、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 FDPS 基因的转录,其转录激活由 SREBP-2(固醇调节元件结合蛋白 2)和 NF-Y 介导。我们还研究了唑来膦酸(一种 FDPS 抑制剂)诱导的细胞增殖是否涉及固醇介导的 FDPS 表达。我们表明,SREBP-2 和 NF-Y 介导的 FDPS 基因转录调控调节细胞增殖。这些结果表明,SREBP-2 和 NF-Y 通过诱导 FDPS 表达来触发细胞增殖,而唑来膦酸的药理作用涉及该途径。