DAX-1 blocks steroid production at multiple levels

被引:153
作者
Lalli, E
Melner, MH
Stocco, DM
Sassone-Corsi, P
机构
[1] Univ Strasbourg 1, INSERM, CNRS, Inst Genet & Biol Mol & Cellulaire, F-67404 Strasbourg, France
[2] Vanderbilt Univ, Sch Med, Dept Obstet & Gynecol, Nashville, TN 37232 USA
[3] Texas Tech Univ, Hlth Sci Ctr, Dept Biochem & Cell Biol, Lubbock, TX 79430 USA
关键词
D O I
10.1210/en.139.10.4237
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
DAX-1 is an unusual member of the nuclear hormone receptor superfamily whose expression is mainly, but not uniquely, restricted to steroidogenic tissues. We have recently shown that DAX-1 can block the first and rate-limiting step in steroid biosynthesis by repressing StAR (steroidogenic acute regulatory protein) expression. Here we show that DAX-1 blocks steroid production at multiple levels in the Y-1 mouse adrenocortical tumor cell line. Expression of DAX-1 in Y-l cells significantly impairs both basal and cAMP-stimulated steroid production, without affecting the functionality of the cAMP-responsive PKA pathway. Experiments using an hydroxylated cholesterol derivative show that biochemical steps in steroidogenesis subsequent to cholesterol delivery to mitochondria are also impaired in Y-1 cells expressing DAX-1. This is explained by the repression of P450scc and 3 beta-HSD expression, in addition to StAR. DAX-1 expression in Y-1 cells results in the inhibition of the activity of the StAR, P450scc and 3 beta-HSD promoters. An inappropriate steroidogenic block. in the male fetus might have an important role in the pathogenesis of sex reversal syndromes caused by a duplication of the genomic region of the X chromosome containing the DAX-1 gene.
引用
收藏
页码:4237 / 4243
页数:7
相关论文
共 42 条
[1]   A DOSAGE SENSITIVE LOCUS AT CHROMOSOME XP21 IS INVOLVED IN MALE TO FEMALE SEX REVERSAL [J].
BARDONI, B ;
ZANARIA, E ;
GUIOLI, S ;
FLORIDIA, G ;
WORLEY, KC ;
TONINI, G ;
FERRANTE, E ;
CHIUMELLO, G ;
MCCABE, ERB ;
FRACCARO, M ;
ZUFFARDI, O ;
CAMERINO, G .
NATURE GENETICS, 1994, 7 (04) :497-501
[2]   TUMOR-NECROSIS-FACTOR-ALPHA ALTERS BOVINE LUTEAL CELL SYNTHETIC CAPACITY AND VIABILITY [J].
BENYO, DF ;
PATE, JL .
ENDOCRINOLOGY, 1992, 130 (02) :854-860
[3]   Acute in vivo inhibition of testosterone by endotoxin parallels loss of steroidogenic acute regulatory (StAR) protein in Leydig cells. [J].
Bosmann, HB ;
Hales, KH ;
Li, XQ ;
Liu, ZM ;
Stocco, DM ;
Hales, DB .
ENDOCRINOLOGY, 1996, 137 (10) :4522-4525
[4]   Characterization of the promoter region of the mouse gene encoding the steroidogenic acute regulatory protein [J].
Caron, KM ;
Ikeda, Y ;
Soo, SC ;
Stocco, DM ;
Parker, KL ;
Clark, BJ .
MOLECULAR ENDOCRINOLOGY, 1997, 11 (02) :138-147
[5]   Submitochondrial distribution of three key steroidogenic proteins (steroidogenic acute regulatory protein and cytochrome p450(scc) and 3 beta-hydroxysteroid dehydrogenase isomerase enzymes) upon stimulation by intracellular calcium in adrenal glomerulosa cells [J].
Cherradi, N ;
Rossier, MF ;
Vallotton, MB ;
Timberg, R ;
Friedberg, I ;
Orly, J ;
Wang, XJ ;
Stocco, DM ;
Capponi, AM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (12) :7899-7907
[6]  
CLARK BJ, 1994, J BIOL CHEM, V269, P28314
[7]  
CLEGG CH, 1987, J BIOL CHEM, V262, P13111
[8]   CYCLIC AMP-DEPENDENT PROTEIN-KINASE CONTROLS BASAL GENE ACTIVITY AND STEROIDOGENESIS IN Y1 ADRENAL-TUMOR CELLS [J].
CLEGG, CH ;
ABRAHAMSEN, MS ;
DEGEN, JL ;
MORRIS, DR ;
MCKNIGHT, GS .
BIOCHEMISTRY, 1992, 31 (14) :3720-3726
[9]   STEROIDOGENIC FACTOR-I BINDING AND TRANSCRIPTIONAL ACTIVITY OF THE CHOLESTEROL SIDE-CHAIN CLEAVAGE PROMOTER IN RAT GRANULOSA-CELLS [J].
CLEMENS, JW ;
LALA, DS ;
PARKER, KL ;
RICHARDS, JS .
ENDOCRINOLOGY, 1994, 134 (03) :1499-1508
[10]   ENDOCRINE AND NEUROGENIC REGULATION OF THE ORPHAN NUCLEAR RECEPTORS NUR77 AND NURR-1 IN THE ADRENAL-GLANDS [J].
DAVIS, IJ ;
LAU, LF .
MOLECULAR AND CELLULAR BIOLOGY, 1994, 14 (05) :3469-3483