Hentschke Moritz, Süsens Ute, Borgmeyer Uwe
Zentrum für Molekulare Neurobiologie, Institut für Entwicklungsneurobiologie, Universität Hamburg, Martinistrasse 52, D-20246 Hamburg, Germany.
Biochem Biophys Res Commun. 2002 Dec 20;299(5):872-9. doi: 10.1016/s0006-291x(02)02753-5.
The mouse nuclear receptor ERRgamma (estrogen receptor-related receptor gamma) is highly expressed in heart, skeletal muscle, kidney, and brain, as well as in the developing nervous system. We found that the expression of the coactivators PGC-1 (PGC-1alpha) and PERC (PGC-1beta) in mammalian cells augmented potently the transcriptional activation by ERRgamma. The constitutive activation function 2 (AF-2) of the orphan receptor was important for the synergistic enhancement. Functional receptor truncation analysis revealed an additional amino-terminal activation function, specific for the ERRgamma2 isoform and PGC-1. In vitro experiments showed a direct interaction of ERRgamma with both coactivators. Our findings suggest distinct regulatory functions for PGC-1 and PERC as tissue-specific coactivators for ERRgamma.
小鼠核受体ERRγ(雌激素受体相关受体γ)在心脏、骨骼肌、肾脏、大脑以及发育中的神经系统中高度表达。我们发现,共激活因子PGC-1(PGC-1α)和PERC(PGC-1β)在哺乳动物细胞中的表达显著增强了ERRγ的转录激活作用。孤儿受体的组成型激活功能2(AF-2)对协同增强作用很重要。功能性受体截短分析揭示了一种额外的氨基末端激活功能,该功能对ERRγ2亚型和PGC-1具有特异性。体外实验表明ERRγ与两种共激活因子直接相互作用。我们的研究结果表明,PGC-1和PERC作为ERRγ的组织特异性共激活因子具有不同的调节功能。