Dufour Catherine R, Wilson Brian J, Huss Janice M, Kelly Daniel P, Alaynick William A, Downes Michael, Evans Ronald M, Blanchette Mathieu, Giguère Vincent
Molecular Oncology Group, McGill University Health Centre, Montréal, Québec H3A 1A1, Canada.
Cell Metab. 2007 May;5(5):345-56. doi: 10.1016/j.cmet.2007.03.007.
Orphan nuclear receptor ERRalpha (NR3B1) is recognized as a key regulator of mitochondrial biogenesis, but it is not known whether ERRalpha and other ERR isoforms play a broader role in cardiac energetics and function. We used genome-wide location analysis and expression profiling to appraise the role of ERRalpha and gamma (NR3B3) in the adult heart. Our data indicate that the two receptors, acting as nonobligatory heterodimers, target a common set of promoters involved in the uptake of energy substrates, production and transport of ATP across the mitochondrial membranes, and intracellular fuel sensing, as well as Ca(2+) handling and contractile work. Motif-finding algorithms assisted by functional studies indicated that ERR target promoters are enriched for NRF-1, CREB, and STAT3 binding sites. Our study thus reveals that the ERRs orchestrate a comprehensive cardiac transcriptional program and further suggests that modulation of ERR activities could be used to manage cardiomyopathies.
孤儿核受体ERRα(NR3B1)被认为是线粒体生物发生的关键调节因子,但ERRα和其他ERR亚型是否在心脏能量代谢和功能中发挥更广泛的作用尚不清楚。我们使用全基因组定位分析和表达谱分析来评估ERRα和γ(NR3B3)在成年心脏中的作用。我们的数据表明,这两种受体作为非必需异二聚体,靶向一组共同的启动子,这些启动子参与能量底物的摄取、ATP在线粒体内膜的产生和运输、细胞内燃料传感,以及Ca(2+)处理和收缩功。功能研究辅助的基序查找算法表明,ERR靶启动子富含NRF-1、CREB和STAT3结合位点。因此,我们的研究揭示了ERRs协调了一个全面的心脏转录程序,并进一步表明调节ERR活性可用于治疗心肌病。