Suppr超能文献

孤儿核受体ERRα和γ对心脏功能的全基因组调控

Genome-wide orchestration of cardiac functions by the orphan nuclear receptors ERRalpha and gamma.

作者信息

Dufour Catherine R, Wilson Brian J, Huss Janice M, Kelly Daniel P, Alaynick William A, Downes Michael, Evans Ronald M, Blanchette Mathieu, Giguère Vincent

机构信息

Molecular Oncology Group, McGill University Health Centre, Montréal, Québec H3A 1A1, Canada.

出版信息

Cell Metab. 2007 May;5(5):345-56. doi: 10.1016/j.cmet.2007.03.007.

Abstract

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.

摘要

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。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验