Picon A, Bertagna X, de Keyzer Y
CNRS UPR 1524, Université René Descartes, Institut Cochin de Génétique Moléculaire, CHU Cochin-Port Royal, Paris, France.
Mol Cell Endocrinol. 1999 Jan 25;147(1-2):93-102. doi: 10.1016/s0303-7207(98)00215-9.
The ectopic ACTH syndrome results from the transcription of the proopiomelanocortin (POMC) gene in non pituitary tumors. To determine its mechanisms, we examined in the human bronchial carcinoma cell line DMS-79 transacting factors binding to the human POMC gene promoter. Three binding sites were identified in the proximal promoter and proteins were studied by gel-shift assays. One of them is a binding site for Nur77/Nurr1 proteins in corticotroph cells but is bound in DMS-79 cells by factor(s) distinct from these proteins. The remaining two binding sites bound yet unidentified proteins and were both functionally active in DMS-79 cells. We also showed that DMS-79 cells lacked a factor required for tissue-restricted POMC gene expression in corticotroph cells. Altogether, our results indicate that POMC gene expression in DMS-79 cells is achieved without several of the corticotroph factors and provide a preliminary characterization of some factors involved in this process. They also reveal that DMS-79 cells are deficient in proteins involved in the regulation by cAMP and glucocorticoids.
异位促肾上腺皮质激素(ACTH)综合征是由非垂体肿瘤中阿黑皮素原(POMC)基因的转录引起的。为了确定其机制,我们在人支气管癌细胞系DMS-79中检测了与人类POMC基因启动子结合的反式作用因子。在近端启动子中鉴定出三个结合位点,并通过凝胶迁移试验研究了相关蛋白质。其中一个是促肾上腺皮质激素细胞中Nur77/Nurr1蛋白的结合位点,但在DMS-79细胞中,与之结合的是不同于这些蛋白的因子。其余两个结合位点结合的是尚未鉴定的蛋白质,且在DMS-79细胞中均具有功能活性。我们还表明,DMS-79细胞缺乏促肾上腺皮质激素细胞中组织特异性POMC基因表达所需的一种因子。总之,我们的结果表明,DMS-79细胞中POMC基因的表达是在缺乏几种促肾上腺皮质激素细胞因子的情况下实现的,并对这一过程中涉及的一些因子进行了初步表征。它们还揭示了DMS-79细胞中参与环磷酸腺苷(cAMP)和糖皮质激素调节的蛋白质存在缺陷。