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Identification of insulin as a novel retinoic acid receptor-related orphan receptor α target gene
- Source :
- FEBS Letters. 588:1071-1079
- Publication Year :
- 2014
- Publisher :
- Wiley, 2014.
-
Abstract
- Insulin plays an important role in regulation of lipid and glucose metabolism. Retinoic acid receptor-related orphan receptor α (RORα) modulates physiopathological processes such as dyslipidemia and diabetes. In this study, we found overexpression of RORα in INS1 cells resulted in increased expression and secretion of insulin. Suppression of endogenous RORα caused a decrease of insulin expression. Luciferase and electrophoretic mobility shift assay (EMSA) assays demonstrated that RORα activated insulin transcription via direct binding to its promoter. RORα was also observed to regulate BETA2 expression, which is one of the insulin active transfactors. In vivo analyses showed that the insulin transcription is increased by the synthetic RORα agonist SR1078. These findings identify RORα as a transcriptional activator of insulin and suggest novel therapeutic opportunities for management of the disease.
- Subjects :
- Male
medicine.medical_specialty
Maf Transcription Factors, Large
medicine.medical_treatment
Biophysics
Gene Expression
Biology
Response Elements
Biochemistry
RAR-related orphan receptor alpha
Retinoic acid-inducible orphan G protein-coupled receptor
Mice
Structural Biology
Internal medicine
Insulin receptor substrate
Consensus Sequence
Insulin Secretion
Basic Helix-Loop-Helix Transcription Factors
Genetics
medicine
Animals
Insulin
Promoter Regions, Genetic
Pancreas
Molecular Biology
Homeodomain Proteins
Orphan receptor
Base Sequence
Promoter
Nuclear Receptor Subfamily 1, Group F, Member 1
Cell Biology
Retinoic acid receptor-related orphan receptor α
Rats
Neuron-derived orphan receptor 1
Mice, Inbred C57BL
Insulin receptor
Retinoic acid receptor
Endocrinology
Gene Expression Regulation
Gene transcription
Trans-Activators
biology.protein
Protein Binding
Subjects
Details
- ISSN :
- 00145793
- Volume :
- 588
- Database :
- OpenAIRE
- Journal :
- FEBS Letters
- Accession number :
- edsair.doi.dedup.....fe9e3f51a2709f260f4f4355b791cb35
- Full Text :
- https://doi.org/10.1016/j.febslet.2014.02.029