GATA factors and androgen receptor collaborate to transcriptionally activate the Rhox5 homeobox gene in Sertoli cells

被引:53
作者
Bhardwaj, Anjana [1 ]
Rao, Manjeet K. [1 ]
Kaur, Ramneet [2 ]
Buttigieg, Miriam R. [1 ]
Wilkinson, Miles F. [1 ]
机构
[1] Univ Texas Houston, MD Anderson Canc Ctr, Unit 1000, Dept Biochem & Mol Biol, Houston, TX 77030 USA
[2] Beth Israel Deaconess Med Ctr, Dept Med, Div Hematol Oncol, Canc Biol Program, Boston, MA 02115 USA
关键词
D O I
10.1128/MCB.01170-07
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
How Sertoli-specific expression is initiated is poorly understood. Here, we address this issue using the proximal promoter (Pp) from the Rhox5 homeobox gene. Its Sertoli cell-specific expression is achieved, in part, through a negative regulatory element that inhibits Pp transcription in non-Sertoli cell lines. Complementing this negative regulation is positive regulation conferred by four androgen-response elements (AREs) that interact with the androgen receptor (AR), a nuclear hormone receptor expressed at high levels in Sertoli cells. A third control mechanism is provided by a consensus GATA-binding site that is crucial for Pp transcription both in vitro and in vivo. Several lines of evidence suggested that GATA factors and AR act cooperatively to activate Pp transcription: (i) the GATA-binding site crucial for Pp transcription is in close proximity to two of the AREs, (ii) GATA and AR form a complex with the Pp in vitro, (iii) overexpression of GATA factors rescued expression from mutant Pp constructs harboring defective AREs, and (iv) incubation of a Sertoli cell line with testosterone triggered corecruitment of AR and GATA4 to the Pp. Collectively, our results suggest that the Rhox5 gene achieves Sertoli cell-specific transcription using a combinatorial strategy involving negative and cooperative positive regulation.
引用
收藏
页码:2138 / 2153
页数:16
相关论文
共 72 条
[1]   ANALYSIS OF THE ANDROGEN RECEPTOR IN ISOLATED TESTICULAR CELL-TYPES WITH A MICROASSAY THAT USES AN AFFINITY LIGAND [J].
ANTHONY, CT ;
KOVACS, WJ ;
SKINNER, MK .
ENDOCRINOLOGY, 1989, 125 (05) :2628-2635
[2]   MOUSE GATA-4 - A RETINOIC ACID-INDUCIBLE GATA-BINDING TRANSCRIPTION FACTOR EXPRESSED IN ENDODERMALLY DERIVED TISSUES AND HEART [J].
ARCECI, RJ ;
KING, AAJ ;
SIMON, MC ;
ORKIN, SH ;
WILSON, DB .
MOLECULAR AND CELLULAR BIOLOGY, 1993, 13 (04) :2235-2246
[3]   New androgen response elements in the murine Pem promoter mediate selective transactivation [J].
Barbulescu, K ;
Geserick, C ;
Schüttke, I ;
Schleuning, WD ;
Haendler, B .
MOLECULAR ENDOCRINOLOGY, 2001, 15 (10) :1803-1816
[4]   GATA-4 is required for sex steroidogenic cell development in the fetal mouse [J].
Bielinska, Malgorzata ;
Seehra, Amrita ;
Toppari, Jorma ;
Heikinheimo, Markku ;
Wilson, David B. .
DEVELOPMENTAL DYNAMICS, 2007, 236 (01) :203-213
[5]   A 3-kilobase region derived from the rat cathepsin L gene directs in vivo expression of a reporter gene in Sertoli cells in a manner comparable to that of the endogenous gene [J].
Charron, M ;
Folmer, JS ;
Wright, WW .
BIOLOGY OF REPRODUCTION, 2003, 68 (05) :1641-1648
[6]  
CHATURVEDI MM, 1994, LYMPHOKINE CYTOK RES, V13, P309
[7]   Role of the transcriptional coactivator CBP/p300 in linking basic helix-loop-helix and CREB responses for follicle-stimulating hormone-mediated activation of the transferrin promoter in Sertoli cells [J].
Chaudhary, J ;
Skinner, MK .
BIOLOGY OF REPRODUCTION, 2001, 65 (02) :568-574
[8]   E-box and cyclic adenosine monophosphate response elements are both required for follicle-stimulating hormone-induced transferrin promoter activation in Sertoli cells [J].
Chaudhary, J ;
Skinner, MK .
ENDOCRINOLOGY, 1999, 140 (03) :1262-1271
[9]   Rapid induction of nuclear transcripts and inhibition of intron decay in response to the polymerase II inhibitor DRB [J].
Clement, JQ ;
Wilkinson, MF .
JOURNAL OF MOLECULAR BIOLOGY, 2000, 299 (05) :1179-1191
[10]   A Sertoli cell-selective knockout of the androgen receptor causes spermatogenic arrest in meiosis [J].
De Gendt, K ;
Swinnen, JV ;
Saunders, PTK ;
Schoonjans, L ;
Dewerchin, M ;
Devos, A ;
Tan, K ;
Atanassova, N ;
Claessens, F ;
Lécureuil, C ;
Heyns, W ;
Carmeliet, P ;
Guillou, F ;
Sharpe, RM ;
Verhoeven, G .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (05) :1327-1332