PDX-1 mediates glucose responsiveness of GAD67, but not GAD65, gene transcription in islets of Langerhans

  • Pedersen A
  • Petersen H
  • Videbak N
 et al. 
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Glucose responsiveness is a fundamental metabolic feature of pancreatic β-cells. Glucose-regulated transcription of the insulin gene is in part mediated via the homeobox transcription factor PDX-1. Another islet protein and diabetes autoantigen, glutamic acid decarboxylase (GAD), has been shown to be subject to regulation by glycemia. We have studied the mRNA level of two isoforms of GAD, GAD65and GAD67, and found that GAD67but not GAD65mRNA steady-state level is regulated by glucose. By transfection of a rat GAD67promoter-driven luciferase reporter gene into primary rat islet cells, we demonstrate glucose-regulated expression of the reporter gene. We show that PDX-1 is able to bind to two TAAT-boxes in the GAD67promoter and that functional disruption of these two PDX-1 binding elements has an additive e6ect in severely impairing glucose responsiveness of the GAD67promoter. These data strongly suggest that PDX-1 is involved in glucose-regulated expression of GAD67. © 2002 Elsevier Science (USA). All rights reserved.

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  • Anette Amstrup Pedersen

  • Helle Vestergaard Petersen

  • Nicoline Videbak

  • Kresten Skak

  • Birgitte Koch Michelsen

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