Agellon L B, Zhang P, Jiang X C, Mendelsohn L, Tall A R
Department of Medicine, Columbia University College of Physicians and Surgeons, New York, New York 10032.
J Biol Chem. 1992 Nov 5;267(31):22336-9.
The plasma cholesteryl ester transfer protein (CETP), primarily synthesized in the liver of several species, is expressed at very low levels in a number of transformed human liver cell lines. The human CETP gene promoter contains a sequence that closely resembles the binding site for the transcription factor CCAAT/enhancer-binding protein (C/EBP). This site is capable of binding C/EBP, as shown by electrophoretic mobility shift and DNase I footprint analyses. Transient expression of the bacterial chloramphenicol acetyltransferase gene under the control of the human CETP gene promotor gave low activities in the human hepatoma cell line, HepG2. However, in the presence of C/EBP, CAT activity was markedly elevated indicating that CETP gene promoter activity was enhanced. In primary cultures of isolated hepatocytes, CETP mRNA was lost rapidly and in parallel with the C/EBP mRNA. C/EBP may play an important role in the proper maintenance of CETP gene promoter activity, and its low levels in proliferating or cultured cells may account for the low level of the CETP gene expression in immortalized human liver cell lines or cultured hepatocytes.
血浆胆固醇酯转运蛋白(CETP)主要在多种物种的肝脏中合成,在一些转化的人肝细胞系中表达水平极低。人CETP基因启动子包含一个与转录因子CCAAT/增强子结合蛋白(C/EBP)的结合位点非常相似的序列。如电泳迁移率变动分析和DNase I足迹分析所示,该位点能够结合C/EBP。在人CETP基因启动子控制下的细菌氯霉素乙酰转移酶基因的瞬时表达在人肝癌细胞系HepG2中活性较低。然而,在存在C/EBP的情况下,氯霉素乙酰转移酶(CAT)活性显著升高,表明CETP基因启动子活性增强。在原代分离肝细胞培养中,CETP mRNA迅速丢失,且与C/EBP mRNA平行。C/EBP可能在CETP基因启动子活性的正常维持中起重要作用,其在增殖或培养细胞中的低水平可能解释了永生化人肝细胞系或培养肝细胞中CETP基因表达水平较低的原因。