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
[11]   MOLECULAR-CLONING AND FUNCTIONAL ANAL OF THE ADENOVIRUS E1A-ASSOCIATED 300-KD PROTEIN (P300) REVEALS A PROTEIN WITH PROPERTIES OF A TRANSCRIPTIONAL ADAPTER [J].
ECKNER, R ;
EWEN, ME ;
NEWSOME, D ;
GERDES, M ;
DECAPRIO, JA ;
LAWRENCE, JB ;
LIVINGSTON, DM .
GENES & DEVELOPMENT, 1994, 8 (08) :869-884
[12]   Hormone-dependent coactivator binding to a hydrophobic cleft on nuclear receptors [J].
Feng, WJ ;
Ribeiro, RCJ ;
Wagner, RL ;
Nguyen, H ;
Apriletti, JW ;
Fletterick, RJ ;
Baxter, JD ;
Kushner, PJ ;
West, BL .
SCIENCE, 1998, 280 (5370) :1747-1749
[13]   Ligand induction of a transcriptionally active thyroid hormone receptor coactivator complex [J].
Fondell, JD ;
Ge, H ;
Roeder, RG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (16) :8329-8333
[14]   Androgen receptor signalling in the prostate [J].
Gnanapragasam, VJ ;
Robson, CN ;
Leung, HY ;
Neal, DE .
BJU INTERNATIONAL, 2000, 86 (09) :1001-1013
[15]  
HARD T, 1993, ACCOUNTS CHEM RES, V26, P644
[16]   SOLUTION STRUCTURE OF THE GLUCOCORTICOID RECEPTOR DNA-BINDING DOMAIN [J].
HARD, T ;
KELLENBACH, E ;
BOELENS, R ;
MALER, BA ;
DAHLMAN, K ;
FREEDMAN, LP ;
CARLSTEDTDUKE, J ;
YAMAMOTO, KR ;
GUSTAFSSON, JA ;
KAPTEIN, R .
SCIENCE, 1990, 249 (4965) :157-160
[17]   FXXLF and WXXLF sequences mediate the NH2-terminal interaction with the ligand binding domain of the androgen receptor [J].
He, B ;
Kemppainen, JA ;
Wilson, EM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (30) :22986-22994
[18]   A signature motif in transcriptional co-activators mediates binding to nuclear receptor [J].
Heery, DM ;
Kalkhoven, E ;
Hoare, S ;
Parker, MG .
NATURE, 1997, 387 (6634) :733-736
[19]   GRIP1, a transcriptional coactivator for the AF-2 transactivation domain of steroid, thyroid, retinoid, and vitamin D receptors [J].
Hong, H ;
Kohli, K ;
Garabedian, MJ ;
Stallcup, MR .
MOLECULAR AND CELLULAR BIOLOGY, 1997, 17 (05) :2735-2744
[20]   Involvement of the TIP60 histone acetylase complex in DNA repair and apoptosis [J].
Ikura, T ;
Ogryzko, VV ;
Grigoriev, M ;
Groisman, R ;
Wang, J ;
Horikoshi, M ;
Scully, R ;
Qin, J ;
Nakatani, Y .
CELL, 2000, 102 (04) :463-473