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Identification and characterization of peroxisome proliferator response element in the mouse GLUT2 promoter
- Source :
- Experimentalmolecular medicine. 37(2)
- Publication Year :
- 2005
-
Abstract
- In the present study, we show that the expression of type 2 glucose transporter isoform (GLUT2) could be regulated by PPAR-gamma in the liver. Rosiglitazone, PPAR-gamma agonist, activated the GLUT2 mRNA level in the primary cultured hepatocytes and Alexander cells, when these cells were transfected with PPAR-gamma/RXR-alpha. We have localized the peroxisome proliferator response element in the mouse GLUT2 promoter by serial deletion studies and site-directed mutagenesis. Chromatin immunoprecipitation assay using ob/ob mice also showed that PPAR-gamma rather than PPAR-alpha binds to the -197/-184 region of GLUT2 promoter. Taken together, liver GLUT2 may be a direct target of PPAR-gamma ligand contributing to glucose transport into liver in a condition when PAPR-gamma expression is increased as in type 2 diabetes or in severe obesity.
- Subjects :
- Male
endocrine system
medicine.medical_specialty
Chromatin Immunoprecipitation
Monosaccharide Transport Proteins
Clinical Biochemistry
Response element
Peroxisome proliferator-activated receptor
Mice, Transgenic
Biology
Response Elements
digestive system
Biochemistry
Rosiglitazone
Mice
Genes, Reporter
Internal medicine
medicine
Animals
Protein Isoforms
PPAR alpha
Promoter Regions, Genetic
Molecular Biology
Transcription factor
Cells, Cultured
chemistry.chemical_classification
Glucose Transporter Type 2
Mice, Inbred ICR
Glucose transporter
Promoter
Transfection
Molecular biology
PPAR gamma
Endocrinology
chemistry
Gene Expression Regulation
Liver
biology.protein
Hepatocytes
Mutagenesis, Site-Directed
Molecular Medicine
GLUT2
lipids (amino acids, peptides, and proteins)
Thiazolidinediones
Chromatin immunoprecipitation
Subjects
Details
- ISSN :
- 12263613
- Volume :
- 37
- Issue :
- 2
- Database :
- OpenAIRE
- Journal :
- Experimentalmolecular medicine
- Accession number :
- edsair.doi.dedup.....5116ae329dda1d3c986d1e6ee810c4f9