DJ-1 positively regulates the androgen receptor by impairing the binding of PIASxα to the receptor

被引:280
作者
Takahashi, K
Taira, T
Niki, T
Seino, C
Iguchi-Ariga, SMM
Ariga, H
机构
[1] Hokkaido Univ, Grad Sch Pharmaceut Sci, Kita Ku, Sapporo, Hokkaido 0600812, Japan
[2] Japan Sci & Technol Corp, Core Res Evolut Sci & Technol, Kawaguchi, Saitama 3320012, Japan
[3] Hokkaido Univ, Coll Med Technol, Kita Ku, Sapporo, Hokkaido 0600812, Japan
关键词
D O I
10.1074/jbc.M101730200
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
DJ-1 was first identified as a novel candidate of the oncogene product that transformed mouse NIH3T3 cells in cooperation with an activated ras. Later DJ-1 was also found to be an infertility-related protein that was reduced in rat sperm treated with sperm toxicants that cause infertility in rats. To determine the functions of DJ-1, cDNAs encoding DJ-1-binding proteins were screened by the yeast two-hybrid method. Of several proteins identified, PIASx alpha /ARIP3, a modulator of androgen receptor (AR), was first characterized as the DJ-1-binding protein in this study. DJ-1 directly bound to the AR-binding region of PIASx alpha by an in vitro coimmunoprecipitation assay and also bound to PIASxa in human 293T cells. Both proteins were co-localized. in the nuclei. PIASx alpha inhibited the AR transcription activity in a dose-dependent manner in cotransfected monkey CV1 cells with an androgen responsive element-luciferase reporter. Introduction of DJ-I into CV1 cells in a state of inhibition of AR activity by PIASx alpha restored AR transcription activity by absorbing PIASx alpha from the AR-PIASx alpha complex, while a DJ-1 mutant harboring an amino acid substitution at number 130 from lysine to arginine did not restore it. These results indicate that DJ-1 is a positive regulator of the androgen receptor.
引用
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页码:37556 / 37563
页数:8
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共 61 条
[1]  
BROWN TR, 1995, J ANDROL, V16, P299
[2]   Functional in vivo interaction between the amino-terminal, transactivation domain and the ligand binding domain of the androgen receptor [J].
Doesburg, P ;
Kuil, CW ;
Berrevoets, CA ;
Steketee, K ;
Faber, PW ;
Mulder, E ;
Brinkmann, AO ;
Trapman, J .
BIOCHEMISTRY, 1997, 36 (05) :1052-1064
[3]   THE STEROID AND THYROID-HORMONE RECEPTOR SUPERFAMILY [J].
EVANS, RM .
SCIENCE, 1988, 240 (4854) :889-895
[4]   Glucocorticoid receptor-glucocorticoid response element binding stimulates nucleosome disruption by the SWI/SNF complex [J].
Farrants, AKO ;
Blomquist, P ;
Kwon, H ;
Wrange, O .
MOLECULAR AND CELLULAR BIOLOGY, 1997, 17 (02) :895-905
[5]   ANATOMY OF THE STEROID-RECEPTOR ZINC FINGER REGION [J].
FREEDMAN, LP .
ENDOCRINE REVIEWS, 1992, 13 (02) :129-145
[6]   Increasing the complexity of coactivation in nuclear receptor signaling [J].
Freedman, LP .
CELL, 1999, 97 (01) :5-8
[7]   Chromatin remodelling by the glucocorticoid receptor requires the BRG1 complex [J].
Fryer, CJ ;
Archer, TK .
NATURE, 1998, 393 (6680) :88-91
[8]   Cloning and characterization of androgen receptor coactivator, ARA55, in human prostate [J].
Fujimoto, N ;
Yeh, SY ;
Kang, HY ;
Inui, S ;
Chang, HC ;
Mizokami, A ;
Chang, CS .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (12) :8316-8321
[9]  
Glass CK, 2000, GENE DEV, V14, P121
[10]   NEW TECHNIQUE FOR ASSAY OF INFECTIVITY OF HUMAN ADENOVIRUS 5 DNA [J].
GRAHAM, FL ;
VANDEREB, AJ .
VIROLOGY, 1973, 52 (02) :456-467