Joseph D R, Sullivan P M, Wang Y M, Millhorn D E, Bayliss D M
Department of Pediatrics, University of North Carolina, Chapel Hill 27599.
J Steroid Biochem Mol Biol. 1991;40(4-6):771-5. doi: 10.1016/0960-0760(91)90302-l.
Extracellular androgen-binding proteins (ABPs) are thought to modulate the regulatory functions of androgens and the trans-acting nuclear androgen receptor. Testicular ABP and plasma sex hormone-binding globulin (SHBG), which is produced in the liver, are encoded by the same gene. We report here that the ABP/SHBG gene is also expressed in fetal rat liver and adult brain. Immunoreactive ABP was localized in the brain and fetal liver and mRNAs were identified in both tissues by northern blot hybridization. Analysis of brain and fetal liver cDNA clones revealed alternatively processed RNAs with sequence characteristics suggesting the encoded proteins could act as competitors of ABP/SHBG binding to cell surface receptors. One cDNA represented a fused transcript of the ABP/SHBG gene and the histidine decarboxylase gene that was apparently formed by a trans-splicing process. Gene sequencing experiments indicate that tissue-specific ABP/SHBG gene promoter-enhancer elements are utilized in testis, brain and fetal liver. These data demonstrate that the structure, RNA transcript processing and likely regulation of the ABP/SHBG gene are very complex.
细胞外雄激素结合蛋白(ABP)被认为可调节雄激素的调节功能以及反式作用核雄激素受体。睾丸ABP和肝脏产生的血浆性激素结合球蛋白(SHBG)由同一基因编码。我们在此报告,ABP/SHBG基因也在胎鼠肝脏和成年大脑中表达。免疫反应性ABP定位于大脑和胎肝,通过Northern印迹杂交在两种组织中均鉴定出mRNA。对大脑和胎肝cDNA克隆的分析揭示了经选择性加工的RNA,其序列特征表明所编码的蛋白质可作为ABP/SHBG与细胞表面受体结合的竞争者。一个cDNA代表ABP/SHBG基因与组氨酸脱羧酶基因的融合转录本,该转录本显然是通过反式剪接过程形成的。基因测序实验表明,组织特异性ABP/SHBG基因启动子-增强子元件在睾丸、大脑和胎肝中被利用。这些数据表明,ABP/SHBG基因的结构、RNA转录本加工以及可能的调控非常复杂。