Repression of HNF1α-mediated transcription by amino-terminal enhancer of split (AES)

被引:3
|
作者
Han, Eun Hee [1 ]
Gorman, Amanda A. [2 ]
Singh, Puja [1 ]
Chi, Young-In [1 ]
机构
[1] Univ Minnesota, Hormel Inst, Sect Struct Biol, Austin, MN 55912 USA
[2] Univ Kentucky, Dept Mol & Cellular Biochem, Lexington, KY 40536 USA
关键词
AES; HNF1; alpha; Homeodomain; POU transcription factor; Protein-protein interaction; Gene regulation; Insulin secretion; Diabetes; HEPATOCYTE NUCLEAR FACTOR-1-ALPHA; PANCREATIC BETA-CELLS; INSULIN-SECRETION; GLUCOSE-METABOLISM; EXPRESSION; YOUNG; GENE; ACTIVATION; MUTATIONS; PROTEINS;
D O I
10.1016/j.bbrc.2015.11.007
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
HNF1 alpha (Hepatocyte Nuclear Factor 1 alpha) is one of the master regulators in pancreatic beta-cell development and function, and the mutations in Hnf1 alpha are the most common monogenic causes of diabetes mellitus. As a member of the POU transcription factor family, HNF1 alpha exerts its gene regulatory function through various molecular interactions; however, there is a paucity of knowledge in their functional complex formation. In this study, we identified the Groucho protein AES (Amino-terminal Enhancer of Split) as a HNF1 alpha-specific physical binding partner and functional repressor of HNF1 alpha-mediated transcription, which has a direct link to glucose-stimulated insulin secretion in beta-cells that is impaired in the HNF1 alpha mutation-driven diabetes. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:14 / 20
页数:7
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