Estrogen stimulates estrogen-related receptor α gene expression through conserved hormone response elements

被引:82
作者
Liu, DX [1 ]
Zhang, ZP [1 ]
Gladwell, W [1 ]
Teng, CT [1 ]
机构
[1] NIEHS, Gene Regulat Sect, Reprod & Dev Toxicol Lab, NIH, Res Triangle Pk, NC 27709 USA
关键词
D O I
10.1210/en.2003-0432
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The estrogen-related receptor alpha gene encodes a nuclear receptor protein, ERRalpha, whose structure is closely related to the estrogen receptors. ERRalpha modulates estrogen receptor ( ER)mediated signaling pathways both positively and negatively. It is selectively expressed in a variety of cell types during development and in adult tissues. We have previously shown that estrogen stimulates the expression of the ERRalpha gene in mouse uterus. In this study, we found that the ERRalpha gene is stimulated by estrogen in mouse uterus and heart but not in liver. Estrogen also stimulates the expression of ERRalpha in the human breast and endometrial cell lines. The human ERRalpha gene promoter contains multiple Sp1 binding sites, and the Sp1 protein is required for the promoter activity. The major estrogen response is mediated by a 34-bp DNA element that contains multiple steroid hormone response element half-sites (MHREs) that are conserved between the human and mouse ERRalpha gene promoters. Mutations made at a single or multiple sites of the MHREs abolished the ER-mediated transcription of the element in transient transfection experiments. By chromatin immunoprecipitation assay, we demonstrated the interaction between ERalpha and MHREs of the endogenous ERRalpha gene promoter in MCF-7 cells. Estrogen treatment further enhanced the association of ERalpha and MHREs in vivo. The present study demonstrated that the ERRalpha gene is a downstream target of ERalpha.
引用
收藏
页码:4894 / 4904
页数:11
相关论文
共 66 条
[1]   Mediator and p300/CBP-steroid receptor coactivator complexes have distinct roles, but function synergistically, during estrogen receptor α-dependent transcription with chromatin templates [J].
Acevedo, ML ;
Kraus, WL .
MOLECULAR AND CELLULAR BIOLOGY, 2003, 23 (01) :335-348
[2]   Estrogenic hormone action in the heart: regulatory network and function [J].
Babiker, FA ;
De Windt, LJ ;
van Eickels, M ;
Grohe, C ;
Meyer, R ;
Doevendans, PA .
CARDIOVASCULAR RESEARCH, 2002, 53 (03) :709-719
[3]   Transcriptional synergism on the pS2 gene promoter between a p160 coactivator and estrogen receptor-α depends on the coactivatior subtype, the type of estrogen response element, and the promoter context [J].
Barkhem, T ;
Haldosén, LA ;
Gustafsson, JÅ ;
Nilsson, S .
MOLECULAR ENDOCRINOLOGY, 2002, 16 (11) :2571-2581
[4]   Estrogen receptor-related receptor impinges on the estrogen axis in bone: Potential function in osteoporosis [J].
Bonnelye, E ;
Kung, V ;
Laplace, C ;
Galson, DL ;
Aubin, JE .
ENDOCRINOLOGY, 2002, 143 (09) :3658-3670
[5]   The ERR-1 orphan receptor is a transcriptional activator expressed during bone development [J].
Bonnelye, E ;
Vanacker, JM ;
Dittmar, T ;
Begue, A ;
Desbiens, X ;
Denhardt, DT ;
Aubin, JE ;
Laudet, V ;
Fournier, B .
MOLECULAR ENDOCRINOLOGY, 1997, 11 (07) :905-916
[6]   Expression of the estrogen-related receptor 1 (ERR-1) orphan receptor during mouse development [J].
Bonnelye, E ;
Vanacker, JM ;
Spruyt, N ;
Alric, S ;
Fournier, B ;
Desbiens, X ;
Laudet, V .
MECHANISMS OF DEVELOPMENT, 1997, 65 (1-2) :71-85
[7]   The orphan nuclear estrogen receptor-related receptor α (ERRα) is expressed throughout osteoblast differentiation and regulates bone formation in vitro [J].
Bonnelye, E ;
Merdad, L ;
Kung, V ;
Aubin, JE .
JOURNAL OF CELL BIOLOGY, 2001, 153 (05) :971-983
[8]   NUCLEAR FACTOR RIP140 MODULATES TRANSCRIPTIONAL ACTIVATION BY THE ESTROGEN-RECEPTOR [J].
CAVAILLES, V ;
DAUVOIS, S ;
LHORSET, F ;
LOPEZ, G ;
HOARE, S ;
KUSHNER, PJ ;
PARKER, MG .
EMBO JOURNAL, 1995, 14 (15) :3741-3751
[9]   ANALYSIS OF SP1 INVIVO REVEALS MULTIPLE TRANSCRIPTIONAL DOMAINS, INCLUDING A NOVEL GLUTAMINE-RICH ACTIVATION MOTIF [J].
COUREY, AJ ;
TJIAN, R .
CELL, 1988, 55 (05) :887-898
[10]   Estrogen receptor null mice: What have we learned and where will they lead us? [J].
Couse, JF ;
Korach, KS .
ENDOCRINE REVIEWS, 1999, 20 (03) :358-417