The thyroid hormone receptor antagonizes CREB-mediated transcription

被引:58
作者
Mendez-Pertuz, M
Sanchez-Pacheco, A
Aranda, A
机构
[1] CSIC, Inst Invest Biomed, E-28029 Madrid, Spain
[2] Univ Autonoma Madrid, Madrid 28029, Spain
关键词
CREB/CREB phosphorylation; thyroid hormone receptor; transcriptional repression;
D O I
10.1093/emboj/cdg295
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
Combinatorial regulation of transcription involves binding of transcription factors to DNA as well as protein-protein interactions between them. In this paper, we demonstrate the existence of a mutual transcriptional antagonism between the thyroid hormone receptor (TR) and the cyclic AMP response element binding protein (CREB), which involves a direct association of both transcription factors. TR inhibits transcriptional activity of CREB and represses activation of cAMP response element (CRE)-containing promoters. TR does not bind to the CRE in vitro, but in viva the liganded receptor is tethered to the promoter through protein-protein interactions. In turn, expression of CREB reduces TR-dependent transcriptional responses. The association of TR with CREB inhibits the ability of protein kinase A to phosphorylate CREB at Ser133, and leads to a reduction in the ligand-dependent recruitment of the p160 coactivators by TR. These results indicate the existence of a transcriptional cross-talk between CREB and TR signalling pathways, which can have important functional consequences.
引用
收藏
页码:3102 / 3112
页数:11
相关论文
共 55 条
[1]   Nuclear hormone receptors and gene expression [J].
Aranda, A ;
Pascual, A .
PHYSIOLOGICAL REVIEWS, 2001, 81 (03) :1269-1304
[2]   ACTIVATION OF CAMP AND MITOGEN RESPONSIVE GENES RELIES ON A COMMON NUCLEAR FACTOR [J].
ARIAS, J ;
ALBERTS, AS ;
BRINDLE, P ;
CLARET, FX ;
SMEAL, T ;
KARIN, M ;
FERAMISCO, J ;
MONTMINY, M .
NATURE, 1994, 370 (6486) :226-229
[3]   MULTIPLE PROTEIN-KINASE A-REGULATED EVENTS ARE REQUIRED FOR TRANSCRIPTIONAL INDUCTION BY CAMP [J].
BRINDLE, P ;
NAKAJIMA, T ;
MONTMINY, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (23) :10521-10525
[4]   Attenuation of a phosphorylation-dependent activator by an HDAC-PP1 complex [J].
Canettieri, G ;
Morantte, I ;
Guzmán, E ;
Asahara, H ;
Herzig, S ;
Anderson, SD ;
Yates, JR ;
Montminy, M .
NATURE STRUCTURAL BIOLOGY, 2003, 10 (03) :175-181
[5]   Role of CBP/P300 in nuclear receptor signalling [J].
Chakravarti, D ;
LaMorte, VJ ;
Nelson, MC ;
Nakajima, T ;
Schulman, IG ;
Juguilon, H ;
Montminy, M ;
Evans, RM .
NATURE, 1996, 383 (6595) :99-103
[6]   Nuclear receptor coactivator ACTR is a novel histone acetyltransferase and forms a multimeric activation complex with P/CAF and CBP/p300 [J].
Chen, HW ;
Lin, RJ ;
Schiltz, RL ;
Chakravarti, D ;
Nash, A ;
Nagy, L ;
Privalsky, ML ;
Nakatani, Y ;
Evans, RM .
CELL, 1997, 90 (03) :569-580
[7]   A TRANSCRIPTIONAL CO-REPRESSOR THAT INTERACTS WITH NUCLEAR HORMONE RECEPTORS [J].
CHEN, JD ;
EVANS, RM .
NATURE, 1995, 377 (6548) :454-457
[8]   The transcriptional integrator CREB-binding protein mediates positive cross talk between nuclear hormone receptors and the hematopoietic bZip protein p45/NF-E2 [J].
Cheng, XB ;
Reginato, MJ ;
Andrews, NC ;
Lazar, MA .
MOLECULAR AND CELLULAR BIOLOGY, 1997, 17 (03) :1407-1416
[9]   PHOSPHORYLATED CREB BINDS SPECIFICALLY TO THE NUCLEAR-PROTEIN CBP [J].
CHRIVIA, JC ;
KWOK, RPS ;
LAMB, N ;
HAGIWARA, M ;
MONTMINY, MR ;
GOODMAN, RH .
NATURE, 1993, 365 (6449) :855-859
[10]   Glucocorticoids repress NF-κB-driven genes by disturbing the interaction of p65 with the basal transcription machinery, irrespective of coactivator levels in the cell [J].
De Bosscher, K ;
Vanden Berghe, W ;
Vermeulen, L ;
Plaisance, S ;
Boone, E ;
Haegeman, G .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (08) :3919-3924