Beyond the allosteric role of Fructose-2,6-bisphosphate: exploring its effects on gene expression and signal transduction.
type: CreativeWork
description: In diabetes, insulin is either not available or not effective in suppressing glucose output by the liver. Enhancing hepatic glucose flux through glycolysis by raising fructose-2,6-bisphosphate (F26BP) levels ameliorates the diabetic phenotype in type 1 and type 2 diabetic mouse models (WU et al. 2001b; WU et al. 2002). This is attributed to the well characterized allosteric effects F26BP has on glucose metabolism enzymes. Recent studies have determined that raising F26BP levels has an additional role in regulating gene expression and signal transduction proteins (WU et al. 2005; WU et al. 2004). In terms of glucose metabolism, raising F26BP levels stimulates glucokinase gene expression and inhibits glucose-6-phosphatase gene expression, thus, also favoring enhanced glycolysis. These effects are not limited to glucose metabolism, as raising F26BP levels in type 2 diabetic mice leads to decreased weight gain and adiposity as well as a decrease in lipogenic enzyme gene expression. To fully characterize this new role of raising F26BP levels on gene expression, a microarray together with iTRAQ proteomic analysis was carried out. Through functional analysis of the microarray biological pathways were identified that changed when F26BP levels were raised in type 2 diabetic mice. In this way a wider array of lipid and cholesterol metabolism genes was shown to be down-regulated. Additionally, several other novel effects of F26BP on gene expression were elucidated. Comparison of the microarray and proteomic datasets elucidated that 87% of the protein expression changes were concomitant with gene expression changes. It is our hypothesis that some of these gene and protein expression changes are mediated through F26BP effect on the insulin signaling pathway component, Akt. Raising F26BP levels in a streptozotocin-treated mouse model (type 1 diabetic) leads to increased Akt levels and phosphorylation at serine-473 (WU et al. 2004). Based on this, experiments were carried out to d…
abstract: In diabetes, insulin is either not available or not effective in suppressing glucose output by the liver. Enhancing hepatic glucose flux through glycolysis by raising fructose-2,6-bisphosphate (F26BP) levels ameliorates the diabetic phenotype in type 1 and type 2 diabetic mouse models (WU et al. 2001b; WU et al. 2002). This is attributed to the well characterized allosteric effects F26BP has on glucose metabolism enzymes. Recent studies have determined that raising F26BP levels has an additional role in regulating gene expression and signal transduction proteins (WU et al. 2005; WU et al. 2004). In terms of glucose metabolism, raising F26BP levels stimulates glucokinase gene expression and inhibits glucose-6-phosphatase gene expression, thus, also favoring enhanced glycolysis. These effects are not limited to glucose metabolism, as raising F26BP levels in type 2 diabetic mice leads to decreased weight gain and adiposity as well as a decrease in lipogenic enzyme gene expression. To fully characterize this new role of raising F26BP levels on gene expression, a microarray together with iTRAQ proteomic analysis was carried out. Through functional analysis of the microarray biological pathways were identified that changed when F26BP levels were raised in type 2 diabetic mice. In this way a wider array of lipid and cholesterol metabolism genes was shown to be down-regulated. Additionally, several other novel effects of F26BP on gene expression were elucidated. Comparison of the microarray and proteomic datasets elucidated that 87% of the protein expression changes were concomitant with gene expression changes. It is our hypothesis that some of these gene and protein expression changes are mediated through F26BP effect on the insulin signaling pathway component, Akt. Raising F26BP levels in a streptozotocin-treated mouse model (type 1 diabetic) leads to increased Akt levels and phosphorylation at serine-473 (WU et al. 2004). Based on this, experiments were carried out to d…
author: Khan, Salmaan Ahmed
language: en_US
keywords: Fructose-2,6-bisphosphatase, Gene set enrichment analysis, glycolysis, Insulin signaling, Lipogenesis, Biochemistry, Molecular Bio, and Biophysics
date published: 2009-09
date modified: 2026-07-24T05:19:44Z
provider: University of Minnesota
publisher: Networked Digital Library of Theses and Dissertations
type: WebPage
source organization: University of Minnesota