Méndez-Pertuz Marinela, Sánchez-Pacheco Aurora, Aranda Ana
Instituto de Investigaciones Biomédicas, Consejo Superior de Investigaciones Científicas, Arturo Duperier 4, 28029 Madrid, Spain.
EMBO J. 2003 Jun 16;22(12):3102-12. doi: 10.1093/emboj/cdg295.
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 vivo 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.
转录的组合调控涉及转录因子与DNA的结合以及它们之间的蛋白质-蛋白质相互作用。在本文中,我们证明了甲状腺激素受体(TR)和环磷酸腺苷反应元件结合蛋白(CREB)之间存在相互转录拮抗作用,这涉及两种转录因子的直接关联。TR抑制CREB的转录活性并抑制含环磷酸腺苷反应元件(CRE)启动子的激活。TR在体外不与CRE结合,但在体内,配体化的受体通过蛋白质-蛋白质相互作用与启动子相连。反过来,CREB的表达会降低TR依赖的转录反应。TR与CREB的关联抑制了蛋白激酶A在Ser133位点磷酸化CREB的能力,并导致TR依赖的p160共激活因子的配体依赖性募集减少。这些结果表明CREB和TR信号通路之间存在转录串扰,这可能具有重要的功能后果。