Dumonteil E, Philippe J
Diabétologie Clinique, Centre Médical Universitaire, Geneva, Switzerland.
Diabetes Metab. 1996 Jun;22(3):164-73.
Insulin, a major hormone of the endocrine pancreas, plays a key role in the control of glucose homeostasis. This review discusses the mechanisms of cell-specific expression and regulation of the insulin gene. Whereas expression is restricted to islet beta-cells in adults, the insulin gene is more widely expressed at several embryonic stages, although the role of extrapancreatic expression is still unclear. beta-cell-specific expression relies on the interactions of 5'-flanking sequence motifs of the promoter with a number of ubiquitous and islet-specific transcription factors. IEF1 and IPF-1, by their binding to the E and A boxes, respectively, of the insulin gene promoter, appear to be the major determinants of beta-cell-specific expression. IEF1 is a heterodimer of the basic helix-loop-helix family of transcription factors, whereas IPF-1 belongs to the homeodomain-containing family. beta-cell specific determinants are conserved throughout evolution, although the human insulin gene 5'-flanking sequence also contains a polymorphic minisatellite which is unique to primates and may play a role in insulin gene regulation. Glucose modulates insulin gene transcription, with multiple elements of the promoter involved in glucose responsiveness. Remarkably, IPF-1 and IEF1 are involved in both beta-cell-specific expression and glucose regulation of the insulin gene. cAMP also regulates insulin gene transcription through a CRE, in response to various hormonal stimuli. On the whole, recent studies have provided a better understanding of beta-cell differentiation and function.
胰岛素是胰腺内分泌的一种主要激素,在葡萄糖稳态的控制中起关键作用。本综述讨论了胰岛素基因细胞特异性表达和调控的机制。尽管在成体中胰岛素的表达局限于胰岛β细胞,但在几个胚胎阶段胰岛素基因的表达更为广泛,尽管胰腺外表达的作用仍不清楚。β细胞特异性表达依赖于启动子的5′侧翼序列基序与许多普遍存在的和胰岛特异性转录因子的相互作用。IEF1和IPF-1分别通过与胰岛素基因启动子的E盒和A盒结合,似乎是β细胞特异性表达的主要决定因素。IEF1是转录因子基本螺旋-环-螺旋家族的异二聚体,而IPF-1属于含同源结构域的家族。β细胞特异性决定因素在整个进化过程中是保守的,尽管人类胰岛素基因5′侧翼序列还包含一个多态性小卫星,这是灵长类动物特有的,可能在胰岛素基因调控中起作用。葡萄糖调节胰岛素基因转录,启动子的多个元件参与葡萄糖反应性。值得注意的是,IPF-1和IEF1都参与胰岛素基因的β细胞特异性表达和葡萄糖调节。cAMP也通过CRE响应各种激素刺激来调节胰岛素基因转录。总体而言,最近的研究对β细胞分化和功能有了更好的理解。