Castelein H, Gulick T, Declercq P E, Mannaerts G P, Moore D D, Baes M I
Laboratory of Clinical Chemistry, Faculty of Pharmaceutical Sciences, Catholic University of Leuven, Belgium.
J Biol Chem. 1994 Oct 28;269(43):26754-8.
A new regulatory element for peroxisome proliferator activated receptor (PPAR)/retinoid X receptor (RXR) heterodimers was found in the promoter of the malic enzyme gene. Similar to previously characterized peroxisome proliferator response elements (PPREs), it consists of a direct repeat of sequences related to the half-site consensus AGGTCA with an interspacing of 1 base pair. Specific binding of PPAR/RXR heterodimers to this element was demonstrated. Furthermore, this sequence conferred ciprofibrate responsiveness of a reporter through the homologous malic enzyme or heterologous thymidine kinase promoters. This PPRE presumably mediates the transcriptional effects of peroxisome proliferators on malic enzyme expression. The presence of a PPRE in the promoter of this lipogenic enzyme suggests a broader function for the PPAR in the regulation of lipid metabolism.
在苹果酸酶基因的启动子中发现了一种新的过氧化物酶体增殖物激活受体(PPAR)/视黄酸X受体(RXR)异二聚体调控元件。与先前鉴定的过氧化物酶体增殖物反应元件(PPRE)相似,它由与半位点共有序列AGGTCA相关的序列直接重复组成,间隔1个碱基对。证实了PPAR/RXR异二聚体与该元件的特异性结合。此外,该序列通过同源苹果酸酶或异源胸苷激酶启动子赋予报告基因环丙贝特反应性。这个PPRE可能介导过氧化物酶体增殖物对苹果酸酶表达的转录作用。这种生脂酶启动子中PPRE的存在表明PPAR在脂质代谢调控中具有更广泛的功能。