Han X, Tuch B E
Pancreas Transplant Unit, Department of Endocrinology, The Prince of Wales Hospital and University of New South Wales, Sydney, Australia.
Comp Biochem Physiol B Biochem Mol Biol. 2001 May;129(1):87-95. doi: 10.1016/s1096-4959(01)00304-9.
The complete porcine preproinsulin cDNA and 1022 bp of its 5'-flanking region have been cloned by PCR-based technology and characterized. The porcine insulin gene has the same structure of three exons and two introns as that found in all insulin genes sequenced to date. Northern blot analysis of isolated adult porcine islets demonstrated an increase in steady-state insulin mRNA levels in response to high concentrations of glucose. Highly conserved cis-acting elements were found in the 5'-flanking region of the porcine insulin gene including multiple E and A elements as well as a cAMP responsive element (CRE). Tissue-specific activity of the proximal promoter was confirmed by transient transfection of the promoter/reporter gene constructs. This information now makes it possible for regulation and expression of the porcine insulin gene to be analyzed.
利用基于聚合酶链反应(PCR)的技术克隆并鉴定了完整的猪胰岛素原前体cDNA及其5'侧翼区的1022bp片段。猪胰岛素基因具有与迄今为止所有已测序胰岛素基因相同的结构,即由三个外显子和两个内含子组成。对分离的成年猪胰岛进行的Northern印迹分析表明,在高浓度葡萄糖刺激下,胰岛素mRNA的稳态水平升高。在猪胰岛素基因的5'侧翼区发现了高度保守的顺式作用元件,包括多个E元件和A元件以及一个环磷酸腺苷(cAMP)反应元件(CRE)。通过启动子/报告基因构建体的瞬时转染证实了近端启动子的组织特异性活性。这些信息使得对猪胰岛素基因的调控和表达进行分析成为可能。