Key Laboratory of Ministry of Education for Gastrointestinal Cancer, Research Center of Molecular Medicine, Fujian Medical University, Fuzhou City 350004, PR China.
Biochimie. 2012 Feb;94(2):384-92. doi: 10.1016/j.biochi.2011.08.006. Epub 2011 Aug 16.
The human liver fatty acid binding protein (hFABP1) participates in cellular long-chain fatty acid trafficking and regulation of lipid metabolism and changes in hFABP1 are associated with an increased risk for type 2 diabetes, cardiovascular disease (CVD), and metabolic syndromes. Gene regulation of hFABP1 is not fully understood. Therefore, in the present study, the full length hFABP1 promoter (nucleotides -2125 to +51) and a series of truncated promoter regions were cloned. A luciferase reporter assay revealed that nucleotides -255 to +50 in the promoter region contained full of maximum hFABP1 promoter activity compared with the full length promoter. Furthermore high activity was shown when the plasmid was transfected into liver-derived cells such as the human hepatoblastoma cell line HepG2 and the hepatoma cell line Huh7. TFSEARCH and TESS programs were used to predict potential transcription factor binding sites. Two putative binding sites for the liver-enriched transcription factors hepatocyte nuclear factor 3β (HNF3β) and CCAAT/enhancer binding protein α (C/EBPα) were identified in the -255 nt to -155 nt hFABP1 promoter region. Site-directed mutagenesis of these two sites reduced dramatically hFABP1 promoter activity. In addition, the electrophoretic mobility shift assay (EMSA) and chromatin immunoprecipitation assay (ChIP) revealed that these binding sites were recognized by HNF3β and C/EBPα respectively. Overexpression of HNF3β and C/EBPα enhanced the transcription of hFABP1 and consequently improved the protein level of hFABP1 in HepG2 cells, while knockdown of HNF3β and C/EBPα showed the inverse effects. Taken together, the hFABP1 gene is highly transcribed in liver-derived cells, and regulated predominantly by liver-enriched transcription factors HNF3β and C/EBPα.
人肝脂肪酸结合蛋白(hFABP1)参与细胞内长链脂肪酸转运和脂质代谢的调节,hFABP1 的变化与 2 型糖尿病、心血管疾病(CVD)和代谢综合征的风险增加有关。hFABP1 的基因调控尚未完全了解。因此,本研究克隆了全长 hFABP1 启动子(核苷酸-2125 至+51)和一系列截短的启动子区域。荧光素酶报告基因检测显示,与全长启动子相比,启动子区域的核苷酸-255 至+50 包含了 hFABP1 启动子活性的全部最大值。此外,当质粒转染到肝源性细胞如人肝癌细胞系 HepG2 和肝癌细胞系 Huh7 时,显示出高活性。TFSEARCH 和 TESS 程序用于预测潜在的转录因子结合位点。在 hFABP1 启动子区域的-255nt 至-155nt 中,发现了两个潜在的富含肝的转录因子肝细胞核因子 3β(HNF3β)和 CCAAT/增强子结合蛋白α(C/EBPα)的结合位点。这两个位点的定点突变大大降低了 hFABP1 启动子的活性。此外,电泳迁移率变动分析(EMSA)和染色质免疫沉淀分析(ChIP)显示,这两个结合位点分别被 HNF3β 和 C/EBPα 识别。HNF3β 和 C/EBPα 的过表达增强了 hFABP1 的转录,从而提高了 HepG2 细胞中 hFABP1 的蛋白水平,而 HNF3β 和 C/EBPα 的敲低则表现出相反的效果。总之,hFABP1 基因在肝源性细胞中高度转录,主要受富含肝的转录因子 HNF3β 和 C/EBPα 调控。