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首页> 外文期刊>Molecular and Cellular Biology >Identification of regulatory sequences and protein-binding sites in the liver-type promoter of a gene encoding 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase.
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Identification of regulatory sequences and protein-binding sites in the liver-type promoter of a gene encoding 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase.

机译:鉴定编码6-磷酸果糖-2-激酶/果糖-2,6-双磷酸酶的基因的肝脏型启动子中的调控序列和蛋白质结合位点。

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摘要

The liver-type and muscle-type isozymes of 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase are encoded by one gene that uses two alternative promoters. We have identified cis-acting sequences and protein-binding sites on the liver-type promoter. Transfection assays with deleted promoters showed that maximal promoter activity is contained within 360 bp upstream of the cap site. DNase I footprinting experiments with liver and spleen nuclear extracts and with purified proteins revealed several protein-binding sites in this region. These included four binding sites for nuclear factor I, one site that contains an octamer consensus but showed a liver-specific footprint pattern, two liver-specific protein-binding sites, and one poly(dG)-containing binding site. Transfection of cells of hepatic origin suggested that all these sites except one are involved in transcriptional regulation. The region between -360 and -2663 contained an element that functioned as a silencer in a nonhepatic cell line. We conclude that in liver transcription from the liver-type promoter of the 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase gene is controlled by ubiquitous and tissue-specific factors and involves activating and derepressing mechanisms.
机译:6-磷酸果糖-2-激酶/果糖-2,6-双磷酸酶的肝型和肌肉型同工酶由使用两个替代启动子的一个基因编码。我们已经确定了肝型启动子上的顺式作用序列和蛋白质结合位点。具有缺失的启动子的转染测定表明最大的启动子活性包含在帽位点上游360 bp之内。用肝脏和脾脏核提取物以及纯化的蛋白质进行的DNase I足迹实验表明,该区域有几个蛋白质结合位点。这些包括核因子I的四个结合位点,一个含有八聚体共有但显示肝脏特异性足迹模式的位点,两个肝脏特异性蛋白结合位点和一个含有聚(dG)的结合位点。肝起源细胞的转染表明,除一个位点外,所有这些位点均参与转录调控。 -360和-2663之间的区域包含一个在非肝细胞系中充当沉默子的元素。我们得出结论,在肝脏中,从6-磷酸果糖-2-激酶/果糖-2,6-双磷酸酶基因的肝型启动子转录受普遍存在的组织特异性因子控制,并涉及激活和抑制机制。

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