Savon S P, Hakimi P, Crawford D R, Klemm D J, Gurney A L, Hanson R W
Department of Biochemistry, Case Western Reserve University School of Medicine, Cleveland, OH 44106-4935, USA.
J Nutr. 1997 Feb;127(2):276-85. doi: 10.1093/jn/127.2.276.
Hepatic expression of the gene for phosphoenolpyruvate carboxykinase (GTP) (PEPCK-C) (EC 4.1.1.32) in birds occurs prior to birth and decreases to negligible levels before hatching, whereas in mammals the gene for PEPCK-C in the liver is expressed at birth and is active throughout the life of the animal. The administration of cyclic AMP to adult chickens results in the induction of transcription of the gene for PEPCK-C and the transient accumulation of PEPCK-C mRNA in the liver. DNase I footprint analysis of 330 bp of the avian PEPCK-C promoter immediately 5' of the start-site of transcription indicated the presence of several protein binding domains, purified CAAT/enhancer binding protein alpha, cAMP regulatory element binding protein and nuclear factor-1 bound to these regions of the promoter. Sequences corresponding to an hepatic nuclear factor-1 binding domain and to the insulin response sequence, previously identified in the rat PEPCK-C promoter, were also found in the chicken PEPCK-C promoter. Co-transfection of an expression vector for CAAT/enhancer binding protein alpha or CAAT/enhancer binding protein beta markedly stimulated transcription from both the chicken and rat PEPCK-C promoters in human hepatoma cells. Sequences involved in the regulation of gene transcription by cyclic AMP and insulin were found to reside between -210 and +1 of the avian PEPCK-C promoter. In general, transcription from the avian promoter was more sensitive to inhibition by insulin than was noted for the rat PEPCK-C promoter, which may explain in part the lack of expression of the gene for PEPCK-C in the livers of adult birds.
鸟类中磷酸烯醇丙酮酸羧激酶(GTP)(PEPCK - C)(EC 4.1.1.32)基因的肝脏表达在出生前就已出现,并在孵化前降至可忽略不计的水平,而在哺乳动物中,肝脏中PEPCK - C基因在出生时表达,并在动物的整个生命过程中保持活跃。给成年鸡注射环磷酸腺苷会导致PEPCK - C基因转录的诱导以及肝脏中PEPCK - C mRNA的短暂积累。对转录起始位点5'端紧邻的330 bp鸟类PEPCK - C启动子进行脱氧核糖核酸酶I足迹分析表明存在几个蛋白质结合结构域,纯化的CAAT/增强子结合蛋白α、环磷酸腺苷反应元件结合蛋白和核因子 - 1结合到启动子的这些区域。在鸡PEPCK - C启动子中也发现了与先前在大鼠PEPCK - C启动子中鉴定的肝核因子 - 1结合结构域和胰岛素反应序列相对应的序列。CAAT/增强子结合蛋白α或CAAT/增强子结合蛋白β的表达载体的共转染显著刺激了人肝癌细胞中鸡和大鼠PEPCK - C启动子的转录。发现环磷酸腺苷和胰岛素调节基因转录所涉及的序列位于鸟类PEPCK - C启动子的 - 210至 +1之间。一般来说,鸟类启动子的转录比大鼠PEPCK - C启动子对胰岛素抑制更敏感,这可能部分解释了成年鸟类肝脏中PEPCK - C基因缺乏表达的原因。