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Diabetes, Vol 48, Issue 3 543-551, Copyright © 1999 by American Diabetes Association
Structure and promoter activity of an islet-specific glucose-6-phosphatase catalytic subunit-related gene
DH Ebert, LJ Bischof, RS Streeper, SC Chapman, CA Svitek, JK Goldman, CE Mathews, EH Leiter, JC Hutton and RM O'Brien
Department of Molecular Physiology and Biophysics, Vanderbilt University Medical School, Nashville, Tennessee 37232-0615, USA.
In liver and kidney, the terminal step in the gluconeogenic pathway is
catalyzed by glucose-6-phosphatase (G-6-Pase). This enzyme is actually a
multicomponent system, the catalytic subunit of which was recently cloned.
Numerous reports have also described the presence of G-6-Pase activity in
islets, although the role of G-6-Pase in this tissue is unclear. Arden and
associates have described the cloning of a novel cDNA that encodes an
islet-specific G-6-Pase catalytic subunit-related protein (IGRP) (Arden SD,
Zahn T, Steegers S, Webb S, Bergman B, O'Brien RM, Hutton JC: Molecular
cloning of a pancreatic islet-specific glucose-6-phosphatase catalytic
subunit related protein (IGRP). Diabetes 48:531-542, 1999). We screened a
mouse BAC library with this cDNA to isolate the IGRP gene, which spans
approximately 8 kbp of genomic DNA. The exon/intron structure of the IGRP
gene has been mapped and, as with the gene encoding the liver/kidney
G-6-Pase catalytic subunit, it is composed of five exons. The sizes of
these exons are 254 (I), 110 (II), 112 (III), 116 (IV), and 1284 (V) bp,
similar to those of the G-6-Pase catalytic subunit gene. Two interspecific
backcross DNA mapping panels were used to unambiguously localize the IGRP
gene (map symbol G6pc-rs) to the proximal portion of mouse chromosome 2.
The IGRP gene transcription start site was mapped by primer extension
analysis, and the activity of the IGRP gene promoter was analyzed in both
the islet-derived HIT cell line and the liver-derived HepG2 cell line. The
IGRP and G-6-Pase catalytic subunit gene promoters show a reciprocal
pattern of activity, with the IGRP promoter being approximately 150-fold
more active than the G-6-Pase promoter in HIT cells.

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Copyright © 1999 by the American Diabetes Association.
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