Tip60 is a co-activator specific for class I nuclear hormone receptors

被引:78
作者
Gaughan, L [1 ]
Brady, ME [1 ]
Cook, S [1 ]
Neal, DE [1 ]
Robson, CN [1 ]
机构
[1] Univ Newcastle Upon Tyne, Sch Med, Prostate Res Grp, Sch Surg Sci, Newcastle Upon Tyne NE2 4HH, Tyne & Wear, England
关键词
D O I
10.1074/jbc.M103710200
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
The nuclear hormone receptor superfamily is composed of a group of hormone-dependent transcription factors that play prominent roles in homeostatic events in vertebrates. A prerequisite for steroid hormone receptor activity is the binding of co-activator molecules to the activation function-2 domain of the receptor. The LXXLL motif/nuclear receptor box, contained within a number of co-activator molecules, mediates the interaction with nuclear hormone receptors. Tip60 (Tat-interactive protein 60 kDa), previously shown to bind to and enhance androgen receptor (AR)-mediated transactivation, contains a single nuclear receptor box at its extreme C terminus. We demonstrate that unlike members of the p160 co-activator family that interact predominantly with the N terminus of the AR in an LXXLL motif-independent manner, the LXXLL motif of Tip60 is required and is sufficient for AR interaction. Furthermore, by using the mammalian two-hybrid system and transient transfection experiments, we show that Tip60 preferentially interacts with and up-regulates class I nuclear receptors, suggesting that Tip60 is a steroid hormone receptor-specific co-activator. We conclude that Tip60 may specifically regulate a subset of nuclear hormone receptors, giving an indication to how regulated nuclear receptor activation can be achieved.
引用
收藏
页码:46841 / 46848
页数:8
相关论文
共 44 条
[21]  
Jenster G, 1999, SEMIN ONCOL, V26, P407
[22]   Identification of a cellular protein that specifically interacts with the essential cysteine region of the HIV-1 tat transactivator [J].
Kamine, J ;
Elangovan, B ;
Subramanian, T ;
Coleman, D ;
Chinnadurai, G .
VIROLOGY, 1996, 216 (02) :357-366
[23]   A possible involvement of TIF1 alpha and TIF1 beta in the epigenetic control of transcription by nuclear receptors [J].
LeDouarin, B ;
Nielsen, AL ;
Garnier, JM ;
Ichinose, H ;
Jeanmougin, F ;
Losson, R ;
Chambon, P .
EMBO JOURNAL, 1996, 15 (23) :6701-6715
[24]  
Li DS, 1999, MOL CELL BIOL, V19, P7191
[25]  
Ma H, 1999, MOL CELL BIOL, V19, P6164
[26]   A new family of nuclear receptor coregulators that integrate nuclear receptor signaling through CREB-binding protein [J].
Mahajan, MA ;
Samuels, HH .
MOLECULAR AND CELLULAR BIOLOGY, 2000, 20 (14) :5048-5063
[27]   THE NUCLEAR RECEPTOR SUPERFAMILY - THE 2ND DECADE [J].
MANGELSDORF, DJ ;
THUMMEL, C ;
BEATO, M ;
HERRLICH, P ;
SCHUTZ, G ;
UMESONO, K ;
BLUMBERG, B ;
KASTNER, P ;
MARK, M ;
CHAMBON, P ;
EVANS, RM .
CELL, 1995, 83 (06) :835-839
[28]   Determinants of coactivator LXXLL motif specificity in nuclear receptor transcriptional activation [J].
McInerney, EM ;
Rose, DW ;
Flynn, SE ;
Westin, S ;
Mullen, TM ;
Krones, A ;
Inostroza, J ;
Torchia, J ;
Nolte, RT ;
Assa-Munt, N ;
Milburn, MV ;
Glass, CK ;
Rosenfeld, MG .
GENES & DEVELOPMENT, 1998, 12 (21) :3357-3368
[29]   FHL2, a novel tissue-specific coactivator of the androgen receptor [J].
Müller, JM ;
Isele, U ;
Metzger, E ;
Rempel, A ;
Moser, M ;
Pscherer, A ;
Breyer, T ;
Holubarsch, C ;
Buettner, R ;
Schüle, R .
EMBO JOURNAL, 2000, 19 (03) :359-369
[30]   Ligand binding and co-activator assembly of the peroxisome proliferator-activated receptor-γ [J].
Nolte, RT ;
Wisely, GB ;
Westin, S ;
Cobb, JE ;
Lambert, MH ;
Kurokawa, R ;
Rosenfeld, MG ;
Willson, TM ;
Glass, CK ;
Milburn, MV .
NATURE, 1998, 395 (6698) :137-143