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Diabetes, Vol 45, Issue 12 1826-1831, Copyright © 1996 by American Diabetes Association
PDX-1 induces insulin and glucokinase gene expressions in alphaTC1 clone 6 cells in the presence of betacellulin
H Watada, Y Kajimoto, J Miyagawa, T Hanafusa, K Hamaguchi, T Matsuoka, K Yamamoto, Y Matsuzawa, R Kawamori and Y Yamasaki
First Department of Medicine, Osaka University School of Medicine, Suita City, Japan.
The pancreatic beta- and alpha-cells are developmentally related to each
other but reveal diverse gene expression patterns. Among the two important
transcription factors for insulin gene expression, IEF1 is present both in
alpha- and beta-cells, but PDX-1/IPF1/STF-1/IDX-1, a homeodomain-containing
transcription factor, is present in beta-cells but not in alpha-cells. To
elucidate the function of PDX-1 in the expression of beta-cell-specific
genes, we established stable alphaTC1 clone 6 (alphaTC1.6)-derived
transfectants expressing PDX-1 and examined the changes in the gene
expression patterns in them. The exogenous expression of PDX-1 in
alphaTC1.6 cells alone could induce islet amyloid polypeptide (IAPP) mRNA
expression in the cells but not the expression of insulin, glucokinase, or
GLUT2 gene. However, when betacellulin was added to the medium, the
PDX-1-expressing alphaTC1.6 cells, but not the control alphaTC1.6 cells,
came to express insulin and glucokinase mRNAs. This did not occur with
other growth factors such as epidermal growth factor, transforming growth
factor alpha, and insulin-like growth factor I. GLUT2 mRNA remained
undetectable in the PDX-1--expressing alphaTC1.6 cells. These observations
demonstrate the potency of PDX-1 for the expression of the insulin,
glucokinase, and IAPP genes and suggest that certain regulatory factors,
which can partially be modified by betacellulin, also contribute to the
beta-cell specificity of gene expression.

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Copyright © 1996 by the American Diabetes Association.
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