Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
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Query: EC:4.1.1.32 (
phosphoenolpyruvate carboxykinase
)
4,204
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
Winged helix/forkhead (Fox) transcription factors have been implicated in the regulation of a number of insulin-responsive genes. The insulin response elements (IREs) of the
phosphoenolpyruvate carboxykinase
(
PEPCK
) and insulin-like growth factor-binding protein-1 (IGFBP-1) genes bind members of the FKHR and HNF3 subclasses of Fox proteins. Previous mutational analyses of the
PEPCK
and IGFBP-1 IREs revealed mutations which do not affect the binding of HNF3 proteins to these elements but do eliminate the ability of the IREs to mediate an insulin response. This dissociation of binding and function provided compelling evidence that HNF3 proteins, per se, are not insulin response proteins. The same approach was used here to determine if
FKHRL1
, a member of the FKHR subclass of Fox proteins, binds to the
PEPCK
and IGFBP-1 IREs in a manner that correlates with the ability of these elements to mediate an insulin response. Overexpression of
FKHRL1
stimulates transcription from transfected reporter constructs that contain a multimerized
PEPCK
IRE or an IGFBP-1 IRE and this stimulation is repressed by insulin. There is a direct correlation between the ability of mutant versions of the
PEPCK
and IGFBP-1 IREs to bind
FKHRL1
and their ability to mediate
FKHRL1
-induced transcription when
FKHRL1
is overexpressed. However, under conditions where
FKHRL1
is not overexpressed, there is a lack of correlation between
FKHRL1
binding to mutant versions of the
PEPCK
and IGFBP-1 IREs and the ability of these elements to mediate an insulin response. Therefore, the
PEPCK
and IGFBP-1 IREs mediate
FKHRL1
-induced transcription and its inhibition by insulin when this protein is overexpressed, but at the normal cellular concentration of
FKHRL1
the insulin response mediated by these elements must involve another protein.
...
PMID:Regulation of phosphoenolpyruvate carboxykinase and insulin-like growth factor-binding protein-1 gene expression by insulin. The role of winged helix/forkhead proteins. 1091 47