Glucocorticoid repression of the mouse gonadotropin-releasing hormone gene is mediated by promoter elements that are recognized by heteromeric complexes containing glucocorticoid receptor

被引:63
作者
Chandran, UR
Attardi, B
Friedman, R
Zheng, ZW
Roberts, JL
DeFranco, DB
机构
[1] UNIV PITTSBURGH, DEPT BIOL SCI, PITTSBURGH, PA 15260 USA
[2] UNIV PITTSBURGH, SCH MED, DEPT MED, PITTSBURGH, PA 15261 USA
[3] MT SINAI SCH MED, ARTHUR M FISHBERG RES CTR NEUROBIOL, NEW YORK, NY 10029 USA
关键词
D O I
10.1074/jbc.271.34.20412
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
We have identified two regions of the mouse gonadotropin-releasing hormone (GnRH) promoter, one between -237 and -201 (distal element) and the other between -184 and -150 (proximal element), which are required for glucocorticoid repression in transiently transfected GT1-7 cells. These sequences show no similarity to known positive or negative glucocorticoid response elements (nGREs) and do not function when placed upstream of heterologous viral promoters. The glucocorticoid receptor (GR) does not bind directly to the distal or proximal promoter elements but may participate in glucocorticoid repression of GdRH gene transcription by virtue of its association within multiprotein complexes at these nGREs. Electrophoretic mobility shift assays with GT1-7 nuclear extract demonstrate the presence of GR-containing protein complexes on GnRH nGREs. One protein that co-occupies the distal nGRE fn vitro along with GR is the POU domain transcription factor Oct-1. Thus, the tethering of Oh to the GnRH distal nGRE, by virtue of a direct or indirect association with DNA-bound Oct-1, could play a role in hormone-dependent transcriptional repression of the GnRH gene. In contrast, Oct-1 does not appear to be a component of the GR-containing protein complex that is bound to the proximal nGRE.
引用
收藏
页码:20412 / 20420
页数:9
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