Synergistic activation of the human type II 3 beta-hydroxysteroid dehydrogenase/Delta(5)-Delta(4) isomerase promoter by the transcription factor steroidogenic factor-1/adrenal 4-binding protein and phorbol ester

被引:152
作者
LeersSucheta, S
Morohashi, K
Mason, JI
Melner, MH
机构
[1] VANDERBILT UNIV,DEPT OBSTET & GYNECOL,SCH MED,NASHVILLE,TN 37232
[2] VANDERBILT UNIV,DEPT CELL BIOL,SCH MED,NASHVILLE,TN 37232
[3] KYUSHU UNIV,GRAD SCH MED SCI,DEPT MOL BIOL,HIGASHI KU,FUKUOKA 812,JAPAN
[4] UNIV EDINBURGH,DEPT CLIN BIOCHEM,EDINBURGH EH3 9YW,MIDLOTHIAN,SCOTLAND
关键词
ORPHAN NUCLEAR RECEPTOR; TYROSINE PHOSPHORYLATION; ADRENAL-HYPERPLASIA; P-450(11-BETA) GENE; GONADAL DEVELOPMENT; RESPONSIVE ELEMENT; KEY REGULATOR; FTZ-F1; GENE; NGFI-B; EXPRESSION;
D O I
10.1074/jbc.272.12.7960
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Steroidogenic factor-1/adrenal 4-binding protein (SF-1/Ad4BP) is an orphan nuclear receptor/transcription factor known to regulate the P450 steroid hydroxylases; however, mechanisms that regulate the activity of SF-1/Ad4BP are not well defined, In addition, little is known about the mechanisms that regulate the human steroidogenic enzyme, type II 3 beta-hydroxysteroid dehydrogenase (3 beta-HSD II), the major gonadal and adrenal isoform, Regulation of the 3 beta-HSD II promoter was examined using human adrenal cortical (H295R; steroidogenic) and cervical (HeLa; non-steroidogenic) carcinoma cells, H295R cells were transfected with a series of 5' deletions of 1251 base pairs (bp) of the 3 beta-HSD II 5'-flanking region fused to a chloramphenicol acetyltransferase (CAT) reporter gene followed by treatment with or without phorbol ester (phorbol 12-myristate 13-acetate; PMA). CAT assay data indicated that the region from -101 to -52 bp of the promoter was required for PMA-induced expression, A putative SF-1/Ad4BP regulatory element, TCAAGGTAA, was identified by sequence homology at -64 to -56 bp of the promoter, Cotransfection of HeLa cells with the -101 3 beta-HSD-CAT construct and an expression vector for SF-1/Ad4BP increased CAT activity 49-fold, Subsequent treatment with PMA induced an unexpected synergistic increase in transcriptional activity 540-fold over basal, Mutation of the putative response element (TCAAGGTAA to TCAATTTAA) abolished SF-1-induced CAT activity and the synergistic response to PMA. Gel mobility shift assays confirmed that SF-II Ad4BP interacts with the putative element and transcripts for SF-1/Ad4BP were detected in H295R cells by Northern analysis, These data are the first to demonstrate 1) regulation of a non-cytochrome P450 steroidogenic enzyme promoter by SF-1/Ad4BP, 2) a powerful synergistic effect of PMA on SF-1/Ad4BP-induced transcription, and 3) the importance of the SF-1/Ad4BP regulatory element in the regulation of the 3 beta-HSD II promoter.
引用
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页码:7960 / 7967
页数:8
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