Nuclear Receptor Cofactors in PPARγ-Mediated Adipogenesis and Adipocyte Energy Metabolism

Transcriptional cofactors are integral to the proper function and regulation of nuclear receptors. Members of the peroxisome proliferator-activated receptor (PPAR) family of nuclear receptors are involved in the regulation of lipid and carbohydrate metabolism. They modulate gene transcription in res...

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Main Authors: Emily Powell, Peter Kuhn, Wei Xu
Format: Article
Language:English
Published: Hindawi Limited 2007-01-01
Series:PPAR Research
Online Access:http://dx.doi.org/10.1155/2007/53843
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spelling doaj-08217f9ea0bb4fb688d70503783c78622020-11-25T00:53:37ZengHindawi LimitedPPAR Research1687-47571687-47652007-01-01200710.1155/2007/5384353843Nuclear Receptor Cofactors in PPARγ-Mediated Adipogenesis and Adipocyte Energy MetabolismEmily Powell0Peter Kuhn1Wei Xu2McArdle Laboratory for Cancer Research, University of Wisconsin, 1400 University Avenue, Madison, WI 53706, USAMcArdle Laboratory for Cancer Research, University of Wisconsin, 1400 University Avenue, Madison, WI 53706, USAMcArdle Laboratory for Cancer Research, University of Wisconsin, 1400 University Avenue, Madison, WI 53706, USATranscriptional cofactors are integral to the proper function and regulation of nuclear receptors. Members of the peroxisome proliferator-activated receptor (PPAR) family of nuclear receptors are involved in the regulation of lipid and carbohydrate metabolism. They modulate gene transcription in response to a wide variety of ligands, a process that is mediated by transcriptional coactivators and corepressors. The mechanisms by which these cofactors mediate transcriptional regulation of nuclear receptor function are still being elucidated. The rapidly increasing array of cofactors has brought into focus the need for a clear understanding of how these cofactors interact in ligand- and cell-specific manners. This review highlights the differential effects of the assorted cofactors regulating the transcriptional action of PPARγ and summarizes the recent advances in understanding the physiological functions of corepressors and coactivators.http://dx.doi.org/10.1155/2007/53843
collection DOAJ
language English
format Article
sources DOAJ
author Emily Powell
Peter Kuhn
Wei Xu
spellingShingle Emily Powell
Peter Kuhn
Wei Xu
Nuclear Receptor Cofactors in PPARγ-Mediated Adipogenesis and Adipocyte Energy Metabolism
PPAR Research
author_facet Emily Powell
Peter Kuhn
Wei Xu
author_sort Emily Powell
title Nuclear Receptor Cofactors in PPARγ-Mediated Adipogenesis and Adipocyte Energy Metabolism
title_short Nuclear Receptor Cofactors in PPARγ-Mediated Adipogenesis and Adipocyte Energy Metabolism
title_full Nuclear Receptor Cofactors in PPARγ-Mediated Adipogenesis and Adipocyte Energy Metabolism
title_fullStr Nuclear Receptor Cofactors in PPARγ-Mediated Adipogenesis and Adipocyte Energy Metabolism
title_full_unstemmed Nuclear Receptor Cofactors in PPARγ-Mediated Adipogenesis and Adipocyte Energy Metabolism
title_sort nuclear receptor cofactors in pparγ-mediated adipogenesis and adipocyte energy metabolism
publisher Hindawi Limited
series PPAR Research
issn 1687-4757
1687-4765
publishDate 2007-01-01
description Transcriptional cofactors are integral to the proper function and regulation of nuclear receptors. Members of the peroxisome proliferator-activated receptor (PPAR) family of nuclear receptors are involved in the regulation of lipid and carbohydrate metabolism. They modulate gene transcription in response to a wide variety of ligands, a process that is mediated by transcriptional coactivators and corepressors. The mechanisms by which these cofactors mediate transcriptional regulation of nuclear receptor function are still being elucidated. The rapidly increasing array of cofactors has brought into focus the need for a clear understanding of how these cofactors interact in ligand- and cell-specific manners. This review highlights the differential effects of the assorted cofactors regulating the transcriptional action of PPARγ and summarizes the recent advances in understanding the physiological functions of corepressors and coactivators.
url http://dx.doi.org/10.1155/2007/53843
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