help button home button Endocrine Society Endocrine Reviews
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS

Endocrine Reviews, doi:10.1210/er.2008-0017
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow Request Copyright Permission
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Giguère, V.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Giguère, V.
Endocrine Reviews 29 (6): 677-696
Copyright © 2008 by The Endocrine Society

Transcriptional Control of Energy Homeostasis by the Estrogen-Related Receptors

Vincent Giguère

The Rosalind and Morris Goodman Cancer Centre and Departments of Biochemistry, Medicine, and Oncology, McGill University, Montréal, Québec, Canada H3A 1A3

Correspondence: Address all correspondence and requests for reprints to: Vincent Giguère, Ph.D., The Rosalind and Morris Goodman Cancer Centre, Cancer Pavilion, 1160 Pine Avenue West, Montreal, Quebec, Canada H3A 1A3. Email: vincent.giguere{at}mcgill.ca.

Transcriptional control of cellular energy metabolic pathways is achieved by the coordinated action of numerous transcription factors and associated coregulators. Several members of the nuclear receptor superfamily have been shown to play important roles in this process because they can translate hormonal, nutrient, and metabolite signals into specific gene expression networks to satisfy energy demands in response to distinct physiological cues. Estrogen-related receptor (ERR) {alpha}, ERRβ, and ERR{gamma} are nuclear receptors that have yet to be associated with a natural ligand and are thus considered as orphan receptors. However, the transcriptional activity of the ERRs is exquisitely sensitive to the presence of coregulatory proteins known to be essential for the control of energy homeostasis, and for all intents and purposes, these coregulators function as protein ligands for the ERRs. In particular, functional genomics and biochemical studies have shown that ERR{alpha} and ERR{gamma} operate as the primary conduits for the activity of members of the family of PGC-1 coactivators. As transcription factors, the ERRs control vast gene networks involved in all aspects of energy homeostasis, including fat and glucose metabolism as well as mitochondrial biogenesis and function. Phenotypic analyses of knockout mouse models have shown that all three ERRs are indispensable for proper development and/or survival of the organism when subjected to a variety of physiological challenges. The focus of this review is on the recent and rapid advances in understanding the functions of the ERRs in regulating bioenergetic pathways, with an emphasis on their roles in the specification of energetic properties required for cell- and tissue-specific functions.




This article has been cited by other articles:


Home page
J. Biol. Chem.Home page
Y.-B. Xie, J.-H. Park, D.-K. Kim, J. H. Hwang, S. Oh, S. B. Park, M. Shong, I.-K. Lee, and H.-S. Choi
Transcriptional Corepressor SMILE Recruits SIRT1 to Inhibit Nuclear Receptor Estrogen Receptor-related Receptor {gamma} Transactivation
J. Biol. Chem., October 16, 2009; 284(42): 28762 - 28774.
[Abstract] [Full Text] [PDF]


Home page
J. Lipid Res.Home page
K. R. Feingold, A. Moser, S. M. Patzek, J. K. Shigenaga, and C. Grunfeld
Infection decreases fatty acid oxidation and nuclear hormone receptors in the diaphragm
J. Lipid Res., October 1, 2009; 50(10): 2055 - 2063.
[Abstract] [Full Text] [PDF]


Home page
Mol. Cell. Biol.Home page
J. Yang, R. S. Williams, and D. P. Kelly
Bcl3 Interacts Cooperatively with Peroxisome Proliferator-Activated Receptor Gamma (PPAR{gamma}) Coactivator 1{alpha} To Coactivate Nuclear Receptors Estrogen-Related Receptor {alpha} and PPAR{alpha}
Mol. Cell. Biol., August 1, 2009; 29(15): 4091 - 4102.
[Abstract] [Full Text] [PDF]


Home page
Cancer Res.Home page
G. Deblois, J. A. Hall, M.-C. Perry, J. Laganiere, M. Ghahremani, M. Park, M. Hallett, and V. Giguere
Genome-Wide Identification of Direct Target Genes Implicates Estrogen-Related Receptor {alpha} as a Determinant of Breast Cancer Heterogeneity
Cancer Res., August 1, 2009; 69(15): 6149 - 6157.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Endocrinology Endocrine Reviews J. Clin. End. & Metab.
Molecular Endocrinology Recent Prog. Horm. Res. All Endocrine Journals
Copyright © 2008 by The Endocrine Society