Zhang D E, Ge X, Rabek J P, Papaconstantinou J
Department of Human Biological Chemistry and Genetics, University of Texas Medical Branch, Galveston 77550.
J Biol Chem. 1991 Nov 5;266(31):21179-85.
The trans-acting factors of the mouse alpha-fetoprotein proximal promoter (-202 base pairs) are aligned as follows: regions Ia (HNF-1), Ib (C/EBP), II (NF-1 or C/EBP), II' (NF-1 or HNF-1), III (NP-III), IV (NP-IV), Va (NP-Va), and Vb (C/EBP). Site-specific mutation abolished protein binding to the corresponding mutated site with the exception of the NF-1 site, in which mutation causes partial protection. Transient expression analyses indicate that chloramphenicol acetyl-transferase (CAT) activity is reduced by mutations in regions Ia, II', Ib, II, and IV. Mutation of region III causes an increased activity and mutation of regions Va and Vb shows a slight inhibitory effect. Linking alpha-fetoprotein enhancer I to the wild type promoter resulted in a 12-fold stimulation of CAT activity. The activity of promoters with mutated C/EBP-binding sites (Ib, II, and Vb), was slightly above controls, indicating that enhancer I can reverse the effect of these mutations. Inhibition or stimulation of promoter activity resulting from mutations of the HNF-1 or NP-III binding sites, respectively, persisted when enhancer I was linked to the promoters, indicating that enhancer I cannot rescue these mutations. Mutation of both HNF-1-binding sites resulted in greater than 90% inhibition of CAT expression with and without enhancer I, indicating these sites are essential for promoter activity. The stimulation of promoter activity by mutation of the NP-III site suggests that this site may be essential for repression or attenuation of the alpha-fetoprotein gene. Our studies indicate that regulation of the alpha-fetoprotein gene requires the combinatorial effect of multiple cis- and trans-acting elements in the proximal promoter and that enhancer I may provide a factor(s) that specifically rescue the promoter from the inhibitory effect of mutation in the C/EBP-binding sites.
小鼠甲胎蛋白近端启动子(-202个碱基对)的反式作用因子排列如下:区域Ia(肝细胞核因子-1,HNF-1)、Ib(C/EBP)、II(核因子-1,NF-1或C/EBP)、II'(NF-1或HNF-1)、III(NP-III)、IV(NP-IV)、Va(NP-Va)和Vb(C/EBP)。位点特异性突变消除了蛋白质与相应突变位点的结合,但NF-1位点除外,该位点的突变导致部分保护作用。瞬时表达分析表明,氯霉素乙酰转移酶(CAT)活性在区域Ia、II'、Ib、II和IV发生突变时降低。区域III的突变导致活性增加,而区域Va和Vb的突变显示出轻微的抑制作用。将甲胎蛋白增强子I与野生型启动子连接导致CAT活性提高了12倍。具有突变的C/EBP结合位点(Ib、II和Vb)的启动子活性略高于对照,表明增强子I可以逆转这些突变的影响。当增强子I与启动子连接时,分别由HNF-1或NP-III结合位点突变导致的启动子活性抑制或刺激作用仍然存在,表明增强子I无法挽救这些突变。两个HNF-1结合位点的突变导致无论有无增强子I,CAT表达均受到大于90%的抑制,表明这些位点对启动子活性至关重要。NP-III位点突变对启动子活性的刺激作用表明,该位点可能对甲胎蛋白基因的抑制或衰减至关重要。我们的研究表明,甲胎蛋白基因的调控需要近端启动子中多个顺式和反式作用元件的组合效应,并且增强子I可能提供一种因子,特异性地将启动子从C/EBP结合位点突变的抑制作用中拯救出来。