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Repression of HNF1α-mediated transcription by amino-terminal enhancer of split (AES).
Han, Eun Hee; Gorman, Amanda A; Singh, Puja; Chi, Young-In.
Afiliação
  • Han EH; Section of Structural Biology, Hormel Institute, University of Minnesota, Austin, MN 55912, USA.
  • Gorman AA; Department of Molecular and Cellular Biochemistry, University of Kentucky, Lexington, KY 40536, USA.
  • Singh P; Section of Structural Biology, Hormel Institute, University of Minnesota, Austin, MN 55912, USA.
  • Chi YI; Section of Structural Biology, Hormel Institute, University of Minnesota, Austin, MN 55912, USA. Electronic address: ychi@hi.umn.edu.
Biochem Biophys Res Commun ; 468(1-2): 14-20, 2015.
Article em En | MEDLINE | ID: mdl-26549228
ABSTRACT
HNF1α (Hepatocyte Nuclear Factor 1α) is one of the master regulators in pancreatic beta-cell development and function, and the mutations in Hnf1α are the most common monogenic causes of diabetes mellitus. As a member of the POU transcription factor family, HNF1α 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 HNF1α-specific physical binding partner and functional repressor of HNF1α-mediated transcription, which has a direct link to glucose-stimulated insulin secretion in beta-cells that is impaired in the HNF1α mutation-driven diabetes.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteínas Repressoras / Células Secretoras de Insulina / Fator 1-alfa Nuclear de Hepatócito Tipo de estudo: Prognostic_studies Limite: Animals / Humans Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteínas Repressoras / Células Secretoras de Insulina / Fator 1-alfa Nuclear de Hepatócito Tipo de estudo: Prognostic_studies Limite: Animals / Humans Idioma: En Ano de publicação: 2015 Tipo de documento: Article