Wei Enhui, Lehner Richard, Vance Dennis E
Department of Biochemistry, CIHR Group on the Molecular and Cell Biology of Lipids, University of Alberta, Edmonton, Alberta T6G 2S2, Canada.
Biochem J. 2005 Jun 15;388(Pt 3):959-66. doi: 10.1042/BJ20041442.
TGH (triacylglycerol hydrolase) catalyses the lipolysis of intracellular stored triacylglycerol. To explore the mechanisms that regulate TGH expression in adipose tissue, we studied the expression of TGH during the differentiation of 3T3-L1 adipocytes. TGH mRNA and protein levels increased dramatically in 3T3-L1 adipocytes compared with pre-adipocytes. Electrophoretic mobility shift assays demonstrated enhanced binding of nuclear proteins of adipocytes to the distal murine TGH promoter region (-542/-371 bp), yielding one adipocyte-specific migrating complex. Competitive and supershift assays demonstrated that the distal TGH promoter fragment bound C/EBPalpha (CCAAT/enhancer-binding protein alpha). Transient transfections of different mutant TGH promoter-luciferase constructs into 3T3-L1 adipocytes and competitive electromobility shift assays showed that the C/EBP-binding elements at positions -470/-459 bp and -404/-390 bp are important for transcriptional activation. Co-transfection with C/EBPalpha cDNA and TGH promoter constructs in 3T3-L1 pre-adipocytes demonstrated that C/EBPalpha increased TGH promoter activity. Ectopic expression of C/EBPalpha in NIH 3T3 cells activated TGH mRNA expression without causing differentiation into adipocytes. These experiments directly link increased TGH expression in adipocytes to transcriptional regulation by C/EBPalpha. This is the first evidence that C/EBPalpha participates directly in the regulation of an enzyme associated with lipolysis.
三酰甘油水解酶(TGH)催化细胞内储存的三酰甘油的脂解作用。为了探究调节脂肪组织中TGH表达的机制,我们研究了3T3-L1脂肪细胞分化过程中TGH的表达情况。与前脂肪细胞相比,3T3-L1脂肪细胞中TGH的mRNA和蛋白质水平显著增加。电泳迁移率变动分析表明,脂肪细胞核蛋白与小鼠TGH启动子远端区域(-542/-371 bp)的结合增强,产生一种脂肪细胞特异性迁移复合物。竞争和超迁移分析表明,TGH启动子远端片段与CCAAT/增强子结合蛋白α(C/EBPα)结合。将不同的突变型TGH启动子-荧光素酶构建体瞬时转染到3T3-L1脂肪细胞中,并进行竞争性电泳迁移率变动分析,结果表明-470/-459 bp和-404/-390 bp位置的C/EBP结合元件对转录激活很重要。在3T3-L1前脂肪细胞中,将C/EBPα cDNA与TGH启动子构建体共转染表明,C/EBPα增加了TGH启动子活性。在NIH 3T3细胞中异位表达C/EBPα可激活TGH mRNA表达,而不会导致细胞分化为脂肪细胞。这些实验直接将脂肪细胞中TGH表达的增加与C/EBPα的转录调控联系起来。这是C/EBPα直接参与调节与脂解相关酶的首个证据。