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This Article Accepted manuscript (PDF) All Versions of this Article: JME-08-0062v1 41/5/315    most recent Alert me when this article is cited Alert me if a correction is posted Services Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Citing Articles Citing Articles via HighWire Citing Articles via Google Scholar Google Scholar Articles by Martin, C. Articles by O'Brien, R. Search for Related Content PubMed PubMed Citation Articles by Martin, C. Articles by O'Brien, R.

C Martin, Molecular Physiology & Biophysics, Vanderbilt University Medical School, Nashville, United States
B Flemming, Molecular Physiology & Biophysics, Vanderbilt University Medical School, Nashville, United States
Y Wang, Molecular Physiology & Biophysics, Vanderbilt University Medical School, Nashville, United States
J Oeser, Molecular Physiology & Biophysics, Vanderbilt University Medical School, Nashville, United States
R O'Brien, Molecular Physiology & Biophysics, Vanderbilt University Medical School, Nashville, United States

Correspondence: Richard O'Brien, Email: richard.obrien{at}vanderbilt.edu

Abstract

Islet-specific glucose-6-phosphatase catalytic subunit-related protein (IGRP/G6PC2) is a major autoantigen in both mouse and human type 1 diabetes. IGRP is selectively expressed in islet beta cells and polymorphisms in the IGRP gene have recently been associated with variations in fasting blood glucose levels and cardiovascular-associated mortality in humans. Chromatin immunoprecipitation (ChIP) assays have shown that the IGRP promoter binds the islet-enriched transcription factors Pax-6 and BETA2. We show here, again using ChIP assays, that the IGRP promoter also binds the islet-enriched transcription factors MafA and Foxa2. Single binding sites for these factors were identified in the proximal IGRP promoter, mutation of which resulted in decreased IGRP fusion gene expression in betaTC-3, HIT and Min6 cells. ChiP assays have shown that the islet-enriched transcription factor Pdx-1 also binds the IGRP promoter but mutational analysis of four Pdx-1 binding sites in the proximal IGRP promoter revealed surprisingly little effect of Pdx-1 binding on IGRP fusion gene expression in betaTC-3 cells. In contrast, in both HIT and Min6 cells mutation of these four Pdx-1 binding sites resulted in an ~50% reduction in fusion gene expression. These data suggest that the same group of islet-enriched transcription factors, namely Pdx-1, Pax-6, MafA, BETA2 and Foxa2 directly or indirectly regulate expression of the two major autoantigens in type 1 diabetes.

This article has been cited by other articles:

				J. C. Hutton and R. M. O'Brien Glucose-6-phosphatase Catalytic Subunit Gene Family J. Biol. Chem., October 23, 2009; 284(43): 29241 - 29245. [Abstract] [Full Text] [PDF]

				C. Dos Santos, P. Bougneres, and D. Fradin A Single-Nucleotide Polymorphism in a Methylatable Foxa2 Binding Site of the G6PC2 Promoter Is Associated With Insulin Secretion In Vivo and Increased Promoter Activity In Vitro Diabetes, February 1, 2009; 58(2): 489 - 492. [Abstract] [Full Text] [PDF]