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Regulatory sequence elements of mouse GLUT4 gene expression in adipose tissues.
- Source :
-
Biochemical and biophysical research communications [Biochem Biophys Res Commun] 2003 Dec 12; Vol. 312 (2), pp. 277-84. - Publication Year :
- 2003
-
Abstract
- Ablation of GLUT4 in adipose tissues results in whole body insulin resistance and high-fat feeding down-regulates GLUT4 mRNA in white adipose tissues. Previous studies demonstrated that adipose tissue specific element(s) (ASE) of the murine GLUT4 gene is located between -551 and -442 relative to transcription start site and that high-fat responsive element(s) (HFRE) for down-regulation of the GLUT4 gene is located between bases -1001 and -442. To further characterize these regulatory elements, the regulation of GLUT4 minigenes containing -701, -551, and -506 bp of 5(')-flanking region was studied in transgenic mice. GLUT4 minigene mRNA from -506 transgenic mice did not express in adipose tissues, indicating that ASE located within 45 bp is located between bases -551 and -506. An 80-kDa of nuclear DNA binding protein was found to bind to a -TCCTCGTGGGAAGCG- element located between bases -551 and -537. High-fat diet feeding down-regulated GLUT4 minigene mRNA in -701 transgenic mice, but not in -551 transgenic mice, indicating that HFRE is located within 150 bp between bases -701 and -551 of the GLUT4 gene and is distinct from ASE.
- Subjects :
- Animals
Base Sequence
Female
Gene Expression Regulation physiology
Glucose Transporter Type 4
Male
Mice
Mice, Inbred C57BL
Mice, Transgenic
Molecular Sequence Data
Organ Specificity
Sequence Analysis, RNA
Tissue Distribution
Adipose Tissue metabolism
Dietary Fats metabolism
Monosaccharide Transport Proteins genetics
Monosaccharide Transport Proteins metabolism
Muscle Proteins
Regulatory Sequences, Ribonucleic Acid genetics
Subjects
Details
- Language :
- English
- ISSN :
- 0006-291X
- Volume :
- 312
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- Biochemical and biophysical research communications
- Publication Type :
- Academic Journal
- Accession number :
- 14637133
- Full Text :
- https://doi.org/10.1016/j.bbrc.2003.10.114