Hormone response of rodent phenylalanine hydroxylase requires HNF1 and the glucocorticoid receptor

被引:14
作者
Bristeau, A [1 ]
Catherin, AM [1 ]
Weiss, MC [1 ]
Faust, DM [1 ]
机构
[1] Inst Pasteur, Dept Biol Mol, CNRS, FRE 2364,Unite Genet Differenciat, F-75724 Paris 15, France
关键词
DNaseI hypersensitive sites; hepatoma cell; cAMP; protein kinase A;
D O I
10.1006/bbrc.2001.5673
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Expression of the rodent phenylalanine hydroxylase (PAH) gene is dependent upon hormones. Induction by glucocorticoids and cAMP occurs slowly and maximal stimulation is obtained by a synergistic effect of the two compounds. Hormone responsiveness is conferred by the tissue-specific HSIII enhancer and involves (i) protein kinase A mediating the cAMP response, even though a consensus sequence for binding of the cAMP response element binding protein is not present; (ii) other serine/threonine kinases as deduced from inhibitor studies; (iii) glucocorticoid receptor protein bound to glucocorticoid response element half sites; and (iv) binding of the liver-enriched transcription factor hepatocyte nuclear factor 1 (HNF1) to sites in the enhancer. Glucocorticoid receptor and HNF1, bound to their cognate sites, cooperatively increase the glucocorticoid response of the PAH gene, this response being synergistically enhanced by cAMP after long-term treatment. (C) 2001 Academic Press.
引用
收藏
页码:852 / 858
页数:7
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