Laganière Josée, Tremblay Gilles B, Dufour Catherine R, Giroux Sylvie, Rousseau François, Giguère Vincent
Molecular Oncology Group, McGill University Health Center, Montréal, Québec H3A 1A1, Canada.
J Biol Chem. 2004 Apr 30;279(18):18504-10. doi: 10.1074/jbc.M313543200. Epub 2004 Feb 20.
The orphan nuclear estrogen-related receptor alpha (ERRalpha) and transcriptional cofactor peroxisome proliferator-activated receptor gamma coactivator-1alpha (PGC-1alpha) are involved in the regulation of energy metabolism. Recently, extensive cross-talk between PGC-1alpha and ERRalpha has been demonstrated. The presence of PGC-1alpha is associated with an elevated expression of ERRalpha, and the two proteins can influence the transcriptional activities of one another. Using a candidate gene approach to detect regulatory variants within genes encoding nuclear receptors, we have identified a 23-bp sequence (ESRRA23) containing two nuclear receptor recognition half-site motifs that is present in 1-4 copies within the promoter of the human ESRRA gene encoding ERRalpha. The ESRRA23 sequence contains a functional ERR response element that is specifically bound by ERRalpha, and chromatin immunoprecipitation shows that endogenous ERRalpha occupies its own promoter in vivo. Strikingly, introduction of PGC-1alpha in HeLa cells by transient transfection induces the activity of the ESRRA promoter in a manner that is dependent on the presence of the ESRRA23 element and on its dosage. Coexpression of ERRalpha and PGC-1alpha results in a synergistic activation of the ESRRA promoter. In experiments using ERRalpha null fibroblasts, the ability of PGC-1alpha to stimulate the ESRRA promoter is considerably reduced but can be restored by addition of ERRalpha. Taken together, these results demonstrate that an interdependent ERRalpha/PGC-1alpha-based transcriptional pathway targets the ESRRA23 element to dictate the level of ERRalpha expression. This study further suggests that this regulatory polymorphism may provide differential responses to ERRalpha/PGC-1alpha-mediated metabolic cues in the human population.
孤儿核雌激素相关受体α(ERRα)和转录辅因子过氧化物酶体增殖物激活受体γ辅激活因子-1α(PGC-1α)参与能量代谢的调节。最近,已证明PGC-1α与ERRα之间存在广泛的相互作用。PGC-1α的存在与ERRα表达升高相关,并且这两种蛋白质可以相互影响转录活性。使用候选基因方法检测编码核受体的基因内的调控变异,我们在编码ERRα的人类ESRRA基因启动子中鉴定出一个23bp序列(ESRRA23),其包含两个核受体识别半位点基序,以1至4个拷贝存在。ESRRA23序列包含一个功能性ERR反应元件,可被ERRα特异性结合,染色质免疫沉淀显示内源性ERRα在体内占据其自身的启动子。引人注目的是,通过瞬时转染在HeLa细胞中引入PGC-1α以依赖于ESRRA23元件的存在及其剂量的方式诱导ESRRA启动子的活性。ERRα和PGC-1α的共表达导致ESRRA启动子的协同激活。在使用ERRα缺失成纤维细胞的实验中,PGC-1α刺激ESRRA启动子的能力大大降低,但可通过添加ERRα恢复。综上所述,这些结果表明基于ERRα/PGC-1α的相互依赖转录途径靶向ESRRA23元件以决定ERRα表达水平。这项研究进一步表明,这种调控多态性可能为人类群体中ERRα/PGC-1α介导的代谢信号提供不同的反应。