STRONG PROMOTER ACTIVITY OF HUMAN AND RAT ISLET AMYLOID POLYPEPTIDE AMYLIN GENE CONSTRUCTS IN MOUSE BETA-CELLS (BETA-TC 3)

被引:10
作者
DEWIT, L
VANMANSFELD, ADM
VANTEEFFELEN, HAAM
LIPS, CJM
HOPPENER, JWM
机构
[1] UNIV UTRECHT,INST MOLEC BIOL & MED BIOTECHNOL,PADUALAAN 8,3584 CH UTRECHT,NETHERLANDS
[2] UNIV UTRECHT,DEPT INTERNAL MED,3584 CH UTRECHT,NETHERLANDS
[3] UNIV UTRECHT,PHYSIOL CHEM LAB,3584 CH UTRECHT,NETHERLANDS
关键词
D O I
10.1006/bbrc.1993.1491
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Islet amyloid polypeptide (IAPP)('amylin') is co-produced with insulin in pancreatic β 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 β cells (particularly in βTC3 cells) than in non-β cells. In both IAPP genes potential transcription elements, with homology to insulin gene transcription elements, were identified. βTC3 cells provide a good model system in which to study regulation of human and rat IAPP gene expression. © 1993 Academic Press, Inc.
引用
收藏
页码:840 / 848
页数:9
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