The LIM-only coactivator FHL2 modulates WT1 transcriptional activity during gonadal differentiation

被引:61
作者
Du, XJ
Hublitz, P
Günther, T
Wilhelm, D
Englert, C
Schüle, R
机构
[1] Univ Freiburg, Klinikum, Frauenklin, D-79106 Freiburg, Germany
[2] Univ Freiburg, Klinikum, Zentrum Klin Forsch, D-79106 Freiburg, Germany
[3] Forschungszentrum Karlsruhe, Inst Genet & Toxikol, D-76021 Karlsruhe, Germany
来源
BIOCHIMICA ET BIOPHYSICA ACTA-GENE STRUCTURE AND EXPRESSION | 2002年 / 1577卷 / 01期
关键词
WT1; transcriptional regulation; FHL2; coactivator; nuclear hormone receptor;
D O I
10.1016/S0167-4781(02)00414-1
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
An essential step during sex determination is the maintenance of the Mullerian duct in females and its regression in males caused by the expression of Mullerian inhibiting substance (MIS). In testes, the Wilms' tumor suppressor and the orphan nuclear receptor SF1 cooperatively bind to the promoter and activate transcription of MIS. In the ovaries, on the other hand, the orphan nuclear receptor DAX1 binds to SF1, inhibits transactivation by WT1/SF1 and thereby suppresses die induction of MIS expression. In addition, WT1 itself is responsible for the upregulation of DAX1 transcription. So far, little is known on which protein-protein interactions or cofactors elicit the spatiotemporal control of WT1-mediated transcription. Here we demonstrate coexpression of the LIM-only coactivator FHL2 and WT1. FHL2 and WT1 functionally interact both in vitro and in vivo. The importance of this interaction is revealed by the ability of FHL2 to potentiate the synergistic induction of MIS gene expression by WT1/SF1. Moreover, FHL2 coactivates transactivation of the DAX1 promoter by WT1. Hence, we present FHL2 as a novel transcriptional coactivator of WT1. The ability to modulate both DAX1 and MIS expression might allow FHL2 to act in the molecular fine tuning of WT1-dependent control mechanisms in the reproductive organs. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:93 / 101
页数:9
相关论文
共 44 条
[1]   Set of optimized luciferase reporter gene plasmids compatible with widely used CAT vectors [J].
Altschmied, J ;
Duschl, J .
BIOTECHNIQUES, 1997, 23 (03) :436-438
[2]   Targeted mutagenesis of the endogenous mouse Mis gene promoter:: In vivo definition of genetic pathways of vertebrate sexual development [J].
Arango, NA ;
Lovell-Badge, R ;
Behringer, RR .
CELL, 1999, 99 (04) :409-419
[3]   THE EXPRESSION OF THE WILMS-TUMOR GENE, WT1, IN THE DEVELOPING MAMMALIAN EMBRYO [J].
ARMSTRONG, JF ;
PRITCHARDJONES, K ;
BICKMORE, WA ;
HASTIE, ND ;
BARD, JBL .
MECHANISMS OF DEVELOPMENT, 1993, 40 (1-2) :85-97
[4]   MULLERIAN-INHIBITING SUBSTANCE FUNCTION DURING MAMMALIAN SEXUAL DEVELOPMENT [J].
BEHRINGER, RR ;
FINEGOLD, MJ ;
CATE, RL .
CELL, 1994, 79 (03) :415-425
[5]   GERMLINE INTRONIC AND EXONIC MUTATIONS IN THE WILMS-TUMOR GENE (WT1) AFFECTING UROGENITAL DEVELOPMENT [J].
BRUENING, W ;
BARDEESY, N ;
SILVERMAN, BL ;
COHN, RA ;
MACHIN, GA ;
ARONSON, AJ ;
HOUSMAN, D ;
PELLETIER, J .
NATURE GENETICS, 1992, 1 (02) :144-148
[6]   FHL2 (SLIM3) is not essential for cardiac development and function [J].
Chu, PH ;
Bardwell, WM ;
Gu, Y ;
Ross, J ;
Chen, J .
MOLECULAR AND CELLULAR BIOLOGY, 2000, 20 (20) :7460-7462
[7]   Nuclear receptor DAX-1 recruits nuclear receptor corepressor N-CoR to steroidogenic factor 1 [J].
Crawford, PA ;
Dorn, C ;
Sadovsky, Y ;
Milbrandt, J .
MOLECULAR AND CELLULAR BIOLOGY, 1998, 18 (05) :2949-2956
[8]   WT1 interacts with the splicing factor U2AF65 in an isoform-dependent manner and can be incorporated into spliceosomes [J].
Davies, RC ;
Calvio, C ;
Bratt, E ;
Larsson, SH ;
Lamond, AI ;
Hastie, ND .
GENES & DEVELOPMENT, 1998, 12 (20) :3217-3225
[9]   A family of LIM-only transcriptional coactivators: Tissue-specific expression and selective activation of CREB and CREM [J].
Fimia, GM ;
De Cesare, D ;
Sassone-Corsi, P .
MOLECULAR AND CELLULAR BIOLOGY, 2000, 20 (22) :8613-8622
[10]   IMPROVED METHOD FOR HIGH-EFFICIENCY TRANSFORMATION OF INTACT YEAST-CELLS [J].
GIETZ, D ;
STJEAN, A ;
WOODS, RA ;
SCHIESTL, RH .
NUCLEIC ACIDS RESEARCH, 1992, 20 (06) :1425-1425