血红素
昼夜节律
生物钟
转录因子
核受体
细胞生物学
化学
生物
葡萄糖稳态
隐色素
心理压抑
生物化学
基因表达
内分泌学
酶
基因
胰岛素抵抗
胰岛素
作者
Lei Yin,Nan Wu,Joshua C. Curtin,Mohammed Qatanani,Nava Szwergold,Robert A. Reid,Gregory M. Waitt,Derek J. Parks,Kenneth H. Pearce,G. Bruce Wisely,Mitchell A. Lazar
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:2007-11-16
卷期号:318 (5857): 1786-1789
被引量:646
标识
DOI:10.1126/science.1150179
摘要
The circadian clock temporally coordinates metabolic homeostasis in mammals. Central to this is heme, an iron-containing porphyrin that serves as prosthetic group for enzymes involved in oxidative metabolism as well as transcription factors that regulate circadian rhythmicity. The circadian factor that integrates this dual function of heme is not known. We show that heme binds reversibly to the orphan nuclear receptor Rev-erbα, a critical negative component of the circadian core clock, and regulates its interaction with a nuclear receptor corepressor complex. Furthermore, heme suppresses hepatic gluconeogenic gene expression and glucose output through Rev-erbα–mediated gene repression. Thus, Rev-erbα serves as a heme sensor that coordinates the cellular clock, glucose homeostasis, and energy metabolism.
科研通智能强力驱动
Strongly Powered by AbleSci AI