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Issue 1061 coverTesticular Cell Dynamics and Endocrine Signaling Volume 1061 published December 2005
Ann. N.Y. Acad. Sci. 1061: 77–93 (2005). doi: 10.1196/annals.1336.009
Copyright © 2005 by the New York Academy of Sciences
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Articles by YU, X.
Articles by MATUSIK, R. J.
Foxa1 and Foxa2 Interact with the Androgen Receptor to Regulate Prostate and Epididymal Genes Differentially

XIUPING YUa, APARNA GUPTAa, YONGQING WANGa, KICHIYA SUZUKIa,b, JANNI MIROSEVICHe, MARIE-CLAIRE ORGEBIN-CRISTb,c,d AND ROBERT J. MATUSIKa,b,d

aDepartment of Urologic Surgery, bCenter for Reproductive Biology Research, cDepartment of Obstetrics and Gynecology, and
dDepartment of Cell and Developmental Biology, Vanderbilt University School of Medicine, Nashville, Tennessee 37232, USA
eMolecular Medicine, Beckman Research Institute at the City of Hope, Duarte, California 91010, USA

Address for correspondence: Robert J. Matusik, Vanderbilt University Medical Center, A-1302 Medical Center North, Nashville, TN 37232-2765. Voice: 615-343-1902; fax: 615-322-8990 robert.matusik{at}vanderbilt.edu

Previous studies from our group have shown that Foxa1 is expressed in the prostate and interacts with the androgen receptor (AR) to regulate prostate-specific genes such as prostate-specific antigen (PSA) and probasin (PB). We report here that Foxa2 but not Foxa1 is expressed in the epididymis. Further, Foxa2 interacts with the AR to regulate the mouse epididymal retinoic acid binding protein (mE-RABP) gene, an epididymis-specific gene. Binding of Foxa2 to the mE-RABP promoter was confirmed by gel-shift and chromatin immunoprecipitation (ChIP) assays. Overexpression of Foxa2 suppresses androgen activation of the mE-RABP promoter while overexpression of Foxa2 with prostate-specific promoters activates gene expression in an androgen-independent manner. GST pull-down assays determined that both Foxa1 and Foxa2 physically interact with the DNA binding domain of the AR. The interaction between Foxa proteins and AR was further confirmed by gel-shift assays where Foxa protein was recruited to AR binding oligomers even when Foxa binding sites were not present, and AR was recruited to Foxa binding oligomers even in the absence of an AR binding site. Given that Foxa1 and Foxa2 proteins are expressed differentially in the prostate and epididymis, these data suggest that the Foxa proteins have distinct effects on AR-regulated genes in different male reproductive accessory organs.

Key Words: epididymis • prostate • Foxa • androgen receptor




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Mol. Endocrinol.Home page
X. Yu, K. Suzuki, Y. Wang, A. Gupta, R. Jin, M.-C. Orgebin-Crist, and R. Matusik
The Role of Forkhead Box A2 to Restrict Androgen-Regulated Gene Expression of Lipocalin 5 in the Mouse Epididymis
Mol. Endocrinol., October 1, 2006; 20(10): 2418 - 2431.
[Abstract] [Full Text] [PDF]



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