GSK4112, a Small Molecule Chemical Probe for the Cell Biology of the Nuclear Heme Receptor Rev-erbα

被引:114
作者
Grant, Daniel [4 ]
Yin, Lei [1 ,2 ,3 ]
Collins, Jon L. [4 ]
Parks, Derek J. [4 ]
Orband-Miller, Lisa A. [4 ]
Wisely, G. Bruce [4 ]
Joshi, Shree [1 ,2 ,3 ]
Lazar, Mitchell A. [1 ,2 ,3 ]
Willson, Timothy M. [4 ]
Zuercher, William J. [4 ]
机构
[1] Univ Penn, Sch Med, Div Endocrinol Diabet & Metab, Dept Med, Philadelphia, PA 19104 USA
[2] Univ Penn, Sch Med, Dept Genet, Philadelphia, PA 19104 USA
[3] Univ Penn, Sch Med, Inst Diabet Obes & Metab, Philadelphia, PA 19104 USA
[4] GlaxoSmithKline Inc, Res Triangle Pk, NC 27707 USA
关键词
CIRCADIAN TRANSCRIPTION; COACTIVATOR PGC-1; IDENTIFICATION; LIGAND; CLOCK; BETA; E75; MECHANISMS; GENE;
D O I
10.1021/cb100141y
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
The identification of nonporphyrin ligands for the orphan nuclear receptor Rev-erb alpha will enable studies of its role as a heme sensor and regulator of metabolic and circadian signaling. We describe the development of a biochemical assay measuring the interaction between Rev-erba and a peptide from the nuclear receptor corepressor-1 (NCoR). The assay was utilized to identify a small molecule ligand for Rev-erba, GSK4112 (1), that was competitive with heme. In cells, 1 profiled as a Rev-erb alpha agonist in cells to inhibit expression of the circadian tar, get gene bmal1. In addition, 1 repressed the expression of gluconeogenic genes in liver cells and reduced glucose output in primary hepatocytes. Therefore, 1 is useful as a chemical tool to probe the function of Rev-erb alpha in transcriptional repression, regulation of circadian biology, and metabolic pathways. Additionally, 1 may serve as a starting point for design of Rev-erba chemical probes with In vivo pharmacological activity.
引用
收藏
页码:925 / 932
页数:8
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