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PMID: 17666523 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, N.I.H., Intramural

Gene expression profiling reveals a regulatory role for ROR alpha and ROR gamma in phase I and phase II metabolism.

Physiological genomics ·Vol. 31 ·No. 2 ·2007-10-22 ·Pages 281-94

Kang HS, Angers M, Beak JY, Wu X, Gimble JM, Wada T, Xie W, Collins JB, Grissom SF, Jetten AM

Abstract

Retinoid-related orphan receptors alpha (ROR alpha) and gamma (ROR gamma) are both expressed in liver; however, their physiological functions in this tissue have not yet been clearly defined. The ROR alpha1 and ROR gamma 1 isoforms, but not ROR alpha 4, show an oscillatory pattern of expression during circadian rhythm. To obtain insight into the physiological functions of ROR receptors in liver, we analyzed the gene expression profiles of livers from WT, ROR alpha-deficient staggerer (sg) mice (ROR alpha(sg/sg)), ROR gamma(-/-), and ROR alpha(sg/sg)ROR gamma(-/-) double knockout (DKO) mice by microarray analysis. DKO mice were generated to study functional redundancy between ROR alpha and ROR gamma. These analyses demonstrated that ROR alpha and ROR gamma affect the expression of a number of genes. ROR alpha and ROR gamma are particularly important in the regulation of genes encoding several phase I and phase II metabolic enzymes, including several 3beta-hydroxysteroid dehydrogenases, cytochrome P450 enzymes, and sulfotransferases. In addition, our results indicate that ROR alpha and ROR gamma each affect the expression of a specific set of genes but also exhibit functional redundancy. Our study shows that ROR alpha and ROR gamma receptors influence the regulation of several metabolic pathways, including those involved in the metabolism of steroids, bile acids, and xenobiotics, suggesting that RORs are important in the control of metabolic homeostasis.

MeSH Terms
Animals Bile Acids and Salts/metabolism Cells, Cultured/metabolism Circadian Rhythm/genetics Cytochrome P-450 Enzyme System/metabolism Female Gene Expression Profiling Hepatocytes/metabolism Lipid Metabolism/genetics Liver/metabolism Metabolic Networks and Pathways/genetics Mice Mice, Inbred C57BL Mice, Knockout Mice, Neurologic Mutants Nuclear Receptor Subfamily 1, Group F, Member 1 Nuclear Receptor Subfamily 1, Group F, Member 3 Receptors, Cytoplasmic and Nuclear/deficiency,genetics,physiology Receptors, Retinoic Acid/deficiency,genetics,physiology Receptors, Thyroid Hormone/deficiency,genetics,physiology Recombinant Fusion Proteins/metabolism Steroids/metabolism Trans-Activators/deficiency,genetics,physiology Transfection Xenobiotics/metabolism
Chemicals
Bile Acids and Salts Nuclear Receptor Subfamily 1, Group F, Member 1 Nuclear Receptor Subfamily 1, Group F, Member 3 Receptors, Cytoplasmic and Nuclear Receptors, Retinoic Acid Receptors, Thyroid Hormone Recombinant Fusion Proteins Rorc protein, mouse Steroids Trans-Activators Xenobiotics Cytochrome P-450 Enzyme System
Authors & Affiliations
10 authors, click to expand affiliations / ORCID
Kang Hong Soon
Cell Biology Section, National Institutes of Health, Research Triangle Park, North Carolina 27709, USA.
Angers Martin
Beak Ju Youn
Wu Xiying
Gimble Jeffrey M
Wada Taira
Xie Wen
Collins Jennifer B
Grissom Sherry F
Jetten Anton M
Article Info
Journal
Physiological genomics
Abbr.
Physiol Genomics
ISSN
1531-2267
Published
2007-10-22
Epub
2007-00-31
Pages
281-94
Language
English
Region
United States
NLM ID
9815683
Subset
IM
Grants
NIDDK NIH HHS · P30 DK072476 · United States
NIDDK NIH HHS · 1P30 DK-072476 · United States
Intramural NIH HHS · United States
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