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Diabetes, Vol 39, Issue 5 523-527, Copyright © 1990 by American Diabetes Association
Glucokinase gene structure. Functional implications of molecular genetic studies
MA Magnuson
Department of Molecular Physiology, Vanderbilt University School of Medicine, Nashville, TN 37232-0615.
Glucokinase is expressed in both the liver and the pancreatic beta-cell and
plays a key role in the metabolism of glucose by both tissues. Expression
of this enzyme is differentially regulated; hepatic glucokinase is
stimulated by insulin and repressed by cAMP, whereas beta-cell glucokinase
activity is increased by glucose. Recently, the glucokinase gene has been
characterized and was found to contain two different transcription control
regions. One region regulates transcription of the gene in the liver,
whereas the other region, which lies at least 12 kilobases further
upstream, controls transcription in the pancreatic beta-cell. The finding
of two different transcription control regions in a single glucokinase gene
provides a genetic basis for the tissue-specific differential regulation of
glucokinase and will serve as the basis for further studies to identify and
characterize the different regulatory elements and factors in the liver and
beta-cell, which are presumably involved. Comparison of different
glucokinase cDNAs isolated from hepatic, insulinoma, and islet cDNA
libraries indicates that at least three glucokinase isoforms are generated
by differential RNA processing of the glucokinase gene transcripts. Whether
any of these glucokinase isoforms are functionally unique remains to be
determined.

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Copyright © 1990 by the American Diabetes Association.
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