Dupriez V J, Darville M I, Antoine I V, Gegonne A, Ghysdael J, Rousseau G G
Hormone and Metabolic Research Unit, University of Louvain Medical School, Brussels, Belgium.
Proc Natl Acad Sci U S A. 1993 Sep 1;90(17):8224-8. doi: 10.1073/pnas.90.17.8224.
6-Phosphofructo-2-kinase (EC 2.7.1.105)/fructose-2,6-bis-phosphatase (EC 3.1.3.46) catalyzes the synthesis and degradation of fructose 2,6-bisphosphate, a ubiquitous stimulator of glycolysis. The liver (L-type) and muscle (M-type) mRNAs for this bifunctional enzyme arise from distinct promoters of the same gene. We have now characterized in rat hepatoma FTO2B cells another mRNA, which is transcribed from a third promoter of that gene. This F-type mRNA is present in fetal rat liver and muscle, in rat placenta, and in several established rat cell lines. The F promoter contains no TATA box but contains several binding sites for Sp1 and for members of the ets oncogene family. Transfection of FTO2B cells with constructs containing the intact or mutagenized F promoter showed that its activity depends mainly on one of these sites. This site bound a heteromeric FTO2B cell protein indistinguishable from the ets-related GA binding protein alpha/ankyrin-repeats GA binding protein beta transcription factor.
6-磷酸果糖-2-激酶(EC 2.7.1.105)/果糖-2,6-二磷酸酶(EC 3.1.3.46)催化果糖2,6-二磷酸的合成与降解,果糖2,6-二磷酸是糖酵解的一种普遍存在的刺激物。这种双功能酶的肝脏(L型)和肌肉(M型)mRNA源自同一基因的不同启动子。我们现在在大鼠肝癌FTO2B细胞中鉴定出另一种mRNA,它是从该基因的第三个启动子转录而来的。这种F型mRNA存在于胎鼠肝脏和肌肉、大鼠胎盘以及几种已建立的大鼠细胞系中。F启动子不含TATA框,但含有几个Sp1以及ets癌基因家族成员的结合位点。用含有完整或诱变F启动子的构建体转染FTO2B细胞表明,其活性主要取决于这些位点中的一个。该位点结合了一种异源FTO2B细胞蛋白,该蛋白与ets相关的GA结合蛋白α/锚蛋白重复GA结合蛋白β转录因子无法区分。