Delegeane A M, Ferland L H, Mellon P L
Regulatory Biology Laboratory, Salk Institute, La Jolla, California 92037.
Mol Cell Biol. 1987 Nov;7(11):3994-4002. doi: 10.1128/mcb.7.11.3994-4002.1987.
We identified and characterized elements which confer tissue specificity and cyclic AMP (cAMP) responsiveness to the human glycoprotein alpha-subunit gene. An enhancer containing an 18-base-pair repeat conferred cAMP responsiveness in a non-tissue-specific fashion. DNase I protection assays revealed DNA-binding factors that bound to this element in both placental and nonplacental cells. It also enhanced the alpha-subunit promoter in a tissue-specific manner but had a negligible effect on a heterologous promoter. A unique element found upstream of this enhancer had no independent activity but, in combination with the cAMP-responsive enhancer, distinctly increased the tissue-specific activity of both the alpha-subunit promoter and a heterologous promoter. A factor that bound to this upstream element was found in placental but not nonplacental cells. We conclude that this novel element acts, perhaps through a specific trans-acting factor, in concert with a cAMP-responsive enhancer to confer tissue specificity to the alpha-subunit gene.
我们鉴定并表征了赋予人糖蛋白α亚基基因组织特异性和环磷酸腺苷(cAMP)反应性的元件。一个含有18个碱基对重复序列的增强子以非组织特异性方式赋予cAMP反应性。DNase I保护试验揭示了在胎盘细胞和非胎盘细胞中均与该元件结合的DNA结合因子。它还以组织特异性方式增强α亚基启动子,但对异源启动子的影响可忽略不计。在该增强子上游发现的一个独特元件没有独立活性,但与cAMP反应性增强子结合后,明显增加了α亚基启动子和异源启动子的组织特异性活性。在胎盘细胞而非非胎盘细胞中发现了一种与该上游元件结合的因子。我们得出结论,这种新元件可能通过一种特定的反式作用因子,与cAMP反应性增强子协同作用,赋予α亚基基因组织特异性。