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人及大鼠胰岛淀粉样多肽/胰淀素基因构建体在小鼠β细胞(βTC 3)中的强启动子活性。

Strong promoter activity of human and rat islet amyloid polypeptide/amylin gene constructs in mouse beta cells (beta TC 3).

作者信息

De Wit L, van Mansfeld A D, van Teeffelen H A, Lips C J, Höppener J W

机构信息

Department of Internal Medicine, Utrecht University, The Netherlands.

出版信息

Biochem Biophys Res Commun. 1993 Apr 30;192(2):840-8. doi: 10.1006/bbrc.1993.1491.

Abstract

Islet amyloid polypeptide (IAPP)('amylin') is co-produced with insulin in pancreatic beta cells and is the formative polypeptide of pancreatic amyloid in patients with type 2 (non-insulin-dependent) diabetes mellitus. Islet amyloid and type 2 diabetes occur in man, but not in rat. To study transcription regulation of IAPP gene expression in man and rat, luciferase reporter constructs containing different portions of the upstream region of both IAPP genes were expressed in transfected cells. Both the human and the rat IAPP gene constructs revealed higher promoter activity in beta cells (particularly in beta TC3 cells) than in non-beta cells. In both IAPP genes potential transcription elements, with homology to insulin gene transcription elements, were identified. beta TC3 cells provide a good model system in which to study regulation of human and rat IAPP gene expression.

摘要

胰岛淀粉样多肽(IAPP)(“胰淀素”)与胰岛素在胰腺β细胞中共同产生,是2型(非胰岛素依赖型)糖尿病患者胰腺淀粉样蛋白的构成多肽。胰岛淀粉样变和2型糖尿病发生在人类,但大鼠不会发生。为了研究人及大鼠IAPP基因表达的转录调控,含有两种IAPP基因上游区域不同部分的荧光素酶报告基因构建体在转染细胞中表达。人和大鼠的IAPP基因构建体在β细胞(特别是βTC3细胞)中均显示出比非β细胞更高的启动子活性。在两种IAPP基因中均鉴定出与胰岛素基因转录元件具有同源性的潜在转录元件。βTC3细胞提供了一个良好的模型系统,可用于研究人和大鼠IAPP基因表达的调控。

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