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Identification of a thyroid hormone response element in the promoter region of the rat lipocalin-type prostaglandin D synthase (β-trace) gene

机译:鉴定大鼠脂质运载蛋白型前列腺素D合酶(β-迹线)基因启动子区域的甲状腺激素反应元件

摘要

We have previously reported that mRNA levels for the rat lipocalin-type prostaglandin (PG) D synthase/β-trace (PGDS) gene, the enzyme responsible for the production of PGD2 in the central nervous system, are regulated by thyroid hormone in vivo. In this study, we describe the identification of a thyroid hormone (T3) response element (T3RE) in the 5'-flanking region of the rat PGDS gene. By radioimmunoprecipitation of genomic fragments using thyroid hormone receptor (TR) protein and specific anti-TR antibodies, gel-shift, foot-printing, mutational analysis, and transactivation assays we have identified a spaced four imperfect direct repeat (DR4) element, GGTTCACTTCAGGGTA (positions -586/-571), which functions as a T3RE when fused to a heterologous promoter. Our results suggest that thyroid hormone regulates the expression of the rat lipocalin-type PGDS gene through this element. Remarkably, the element identified also confers regulation by retinoic acid. Giving the important roles proposed for the PGDS enzyme and its product, PGD2, the major PG in the mammalian brain, the altered expression of the PGDS gene may contribute to the deleterious effects of hypothyroidism in the central nervous system.
机译:我们以前曾报道过,大鼠脂质运载蛋白型前列腺素(PG)D合酶/β-迹线(PGDS)基因(负责中枢神经系统中PGD2产生的酶)的mRNA水平在体内受到甲状腺激素的调节。在这项研究中,我们描述了大鼠PGDS基因5'侧翼区域中甲状腺激素(T3)反应元件(T3RE)的鉴定。通过使用甲状腺激素受体(TR)蛋白和特异性抗TR抗体对基因组片段进行放射免疫沉淀,凝胶移位,印迹,突变分析和反式激活分析,我们确定了四个不完美的直接重复(DR4)元件,即GGTTCACTTCAGGGTA(位置-586 / -571),当与异源启动子融合时起T3RE的作用。我们的研究结果表明,甲状腺激素通过该元素调节大鼠脂钙素型PGDS基因的表达。值得注意的是,鉴定出的元素也赋予视黄酸调节作用。鉴于拟议中的PGDS酶及其产物PGD2(哺乳动物脑中的主要PG)具有重要作用,PGDS基因表达的改变可能有助于中枢神经系统甲状腺功能减退的有害作用。

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