Identification of SR8278, a Synthetic Antagonist of the Nuclear Heme Receptor REV-ERB

被引:145
作者
Kojetin, Douglas [1 ]
Wang, Yongjun [1 ]
Kamenecka, Theodore M. [1 ]
Burris, Thomas P. [1 ]
机构
[1] Scripps Res Inst, Jupiter, FL 33458 USA
基金
美国国家卫生研究院;
关键词
CIRCADIAN TRANSCRIPTION; ALPHA; LIGAND; GENE;
D O I
10.1021/cb1002575
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
REV-ERB alpha is a member of the nuclear receptor superfamily that functions as a receptor for the porphoryin heme. REV-ERB alpha suppresses transcription of its target genes in a heme-dependent manner. Recently, the first nonporphyrin synthetic ligand for REV-ERB alpha, GSK4112, was designed, and it mimics the action of heme acting as agonist. Here, we report the identification of the first REV-ERB antagonist, SR8278. SR8278 is structurally similar to the agonist but blocks the ability of the GSK4112 to enhance REV-ERB alpha-dependent repression in a cotransfection assay. Additionally, whereas GSK4112 suppresses the expression of REV-ERB alpha target genes involved in gluconeogenesis, SR8278 stimulates the expression of these genes. Thus, SR8278 represents a unique chemical tool for probing REV-ERB function and may serve as a point for initiation of further optimization to develop REV-ERB antagonists with the ability to explore circadian and metabolic functions.
引用
收藏
页码:131 / 134
页数:4
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