Cortright D N, Goosens K A, Lesh J S, Seasholtz A F
Department of Biological Chemistry, The University of Michigan, Ann Arbor 48109-0720, USA.
Endocrinology. 1997 May;138(5):2098-108. doi: 10.1210/endo.138.5.5128.
The CRH-binding protein (CRH-BP) antagonizes the ACTH-releasing activity of the neuropeptide CRH in vitro. However, the function of CRH-BP in vivo and the molecular mechanisms that regulate CRH-BP expression are not well understood. In this study, the rat CRH-BP gene was characterized, and CRH-BP promoter sequences were identified. The rat CRH-BP gene spans almost 12 kilobases and contains 7 exons. Ribonuclease protection experiments indicate that transcription of the CRH-BP gene initiates at multiple sites in rat cerebral cortex. Transfection experiments with CRH-BP-reporter constructs, containing 88-3500 bp 5' flanking and 66 bp 5' untranslated DNA from the rat CRH-BP gene, demonstrate basal promoter activity in multiple cell lines. CRH-BP-reporter constructs also demonstrate positive regulation of promoter activity by cAMP in a variety of cell lines and by CRH in cells expressing the CRH receptor. The DNA sequences between -341 and -88 bp, including the cAMP response element-like sequence at -127 bp, are required for maximal cAMP and CRH regulation of CRH-BP promoter activity. These studies suggest that CRH-BP transcription in vivo may be positively regulated by cAMP and CRH.
促肾上腺皮质激素释放激素结合蛋白(CRH-BP)在体外可拮抗神经肽CRH的促肾上腺皮质激素(ACTH)释放活性。然而,CRH-BP在体内的功能以及调节CRH-BP表达的分子机制尚不清楚。在本研究中,对大鼠CRH-BP基因进行了表征,并鉴定了CRH-BP启动子序列。大鼠CRH-BP基因跨度近12千碱基,包含7个外显子。核糖核酸酶保护实验表明,CRH-BP基因在大鼠大脑皮层的多个位点起始转录。用含有大鼠CRH-BP基因88 - 3500 bp 5'侧翼和66 bp 5'非翻译DNA的CRH-BP报告基因构建体进行转染实验,证明在多种细胞系中具有基础启动子活性。CRH-BP报告基因构建体还表明,在多种细胞系中,cAMP可对启动子活性产生正向调节作用,而在表达CRH受体的细胞中,CRH也可对启动子活性产生正向调节作用。对于CRH-BP启动子活性的最大cAMP和CRH调节作用,需要-341至-88 bp之间的DNA序列,包括-127 bp处的cAMP反应元件样序列。这些研究表明,体内CRH-BP转录可能受到cAMP和CRH的正向调节。