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Vol. 59, Issue 3, 567-575, March 2001
Department of Molecular Genetics, Novo Nordisk A/S, Bagsvaerd,
Denmark
Thiazolidinediones (TZDs) are a new class of compounds that improve the
insulin sensitivity in patients with non-insulin-dependent diabetes
mellitus (NIDDM) as well as in rodent models of NIDDM. These compounds
act as high-affinity ligands for a member of the nuclear hormone
receptor superfamily PPAR
, which has been shown to play an important
role in adipocyte differentiation. The strong correlation between the
antidiabetic activity of TZDs and their ability to activate PPAR
has
led to suggestions that PPAR
or downstream regulated genes mediate
the effects of TZDs. To identify novel genes that potentially mediate
the effects of TZDs, we have isolated genes that are differentially
expressed during thiazolidinedione-stimulated differentiation of 3T3-L1
cells. Using mRNA differential display, we have compared 3T3-L1 cells
treated to differentiate in the presence of BRL49653 with untreated
3T3-L1 cells and identified Fos-related antigen 1 (Fra-1), a member of
the Fos protein family, as a novel molecular target for BRL49653 action
in 3T3-L1 cells. Analysis of all members of the Fos-Jun family of
transcription factors showed that Fra-1 was the only member that was
specifically up-regulated by BRL49653. The only other member of the
Fos-Jun family expressed in differentiated 3T3-L1 cells was JunD and a complex of Fra-1 and JunD was formed on a consensus AP-1 binding element in differentiated 3T3-L1 cells, suggesting that the complex of
Fra-1 and JunD may play a role in the stimulation of the
differentiation process of 3T3-L1 cells observed after treatment of the
cells with insulin sensitizers.
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