Ohba T, Holt J A, Billheimer J T, Strauss J F
Department of Obstetrics and Gynecology, University of Pennsylvania School of Medicine, Philadelphia 19104, USA.
Biochemistry. 1995 Aug 22;34(33):10660-8. doi: 10.1021/bi00033a042.
The human sterol carrier protein x (SCPx)/sterol carrier protein 2 (SCP2) gene gives rise to two mRNAs: a 2.8 kb mRNA encoding SCPx, a peroxisome-associated thiolase, and a 1.5 kb mRNA encoding SCP2, which is thought to be an intracellular lipid transfer protein. The SCPx/SCP2 gene is highly expressed in organs involved in lipid metabolism, but the relative abundance of SCPx and SCP2 mRNAs varies. Here we report that the two transcripts are produced under the direction of two independent promoters. We determined the DNA sequence of 3.4 kb of the proximal promoter governing the transcription of SCPx sequences. The promoter governing the transcription of SCP2 sequences was identified 45 kb downstream from the SCPx promoter in intron XI. This promoter initiates transcription within exon XII. Both the SCPx and SCP2 promoters lack TATA boxes and initiate transcription at multiple sites. They share features that are found in the promoters of genes encoding other peroxisomal proteins. The basal activities of the two promoters were tested as fusion gene constructs in selected host cells, including BeWo choriocarcinoma cells, HepG2 hepatoblastoma cells, murine Y1 adrenocortical tumor cells, and Balb 3T3 fibroblasts. Cell host-specific patterns of promoter activity were observed. In addition, 8-Br-cAMP and phorbol myristate acetate were found to increase SCPx promoter activity in a host cell-specific manner. The SCP2 promoter was not significantly influenced by these agents.(ABSTRACT TRUNCATED AT 250 WORDS)
人类固醇载体蛋白X(SCPx)/固醇载体蛋白2(SCP2)基因产生两种mRNA:一种2.8 kb的mRNA编码SCPx,一种与过氧化物酶体相关的硫解酶;另一种1.5 kb的mRNA编码SCP2,它被认为是一种细胞内脂质转运蛋白。SCPx/SCP2基因在参与脂质代谢的器官中高度表达,但SCPx和SCP2 mRNA的相对丰度有所不同。在此我们报告,这两种转录本是在两个独立启动子的指导下产生的。我们测定了调控SCPx序列转录的近端启动子3.4 kb的DNA序列。调控SCP2序列转录的启动子在第XI内含子中位于SCPx启动子下游45 kb处被鉴定出来。该启动子在外显子XII内启动转录。SCPx和SCP2启动子均缺乏TATA盒,并在多个位点启动转录。它们具有在编码其他过氧化物酶体蛋白的基因启动子中发现的特征。在选定的宿主细胞中,包括BeWo绒毛膜癌细胞、HepG2肝母细胞瘤细胞、小鼠Y1肾上腺皮质肿瘤细胞和Balb 3T3成纤维细胞,将这两个启动子作为融合基因构建体测试其基础活性。观察到了细胞宿主特异性的启动子活性模式。此外,发现8-溴环磷酸腺苷(8-Br-cAMP)和佛波醇肉豆蔻酸酯乙酸盐以宿主细胞特异性方式增加SCPx启动子活性。这些试剂对SCP2启动子没有显著影响。(摘要截短于250字)