PGC-1agr: A Multifunctional Transcriptional Coactivator Involved in Human Metabolic Disorders

Authors: H. Oberkofler1; F. Krempler1; W. Patsch1

Source: Current Genomics, Volume 5, Number 5, July 2004 , pp. 443-451(9)

Publisher: Bentham Science Publishers

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Abstract:

Nuclear hormone receptor function is controlled by a number of ancillary factors termed coregulators. Such coactivators and corepressors afford considerable flexibility in the coordinate expression of gene networks in numerous physiological, developmental and metabolic processes. PGC-1agr, originally described as transcriptional coactivator of PPARggr, has since been shown to act in a much broader context. PGC-1agr coordinates the transcriptional programs of several key cellular pathways including mitochondrial biogenesis, thermogenesis, hepatic gluconeogenesis and bgr- oxidation of fatty acids via interactions with a growing number of transcription factors. A central issue to understand the diverse functions of PGC-1agr is to gain insight into the mechanisms that confer specificity to its interactions with transfactors in response to intra- and extracellular signals. This review focuses on the different modes of regulation of PGC-1agr function and the implications for tissue and context-specific transcriptional responses. Moreover, the role of sequence substitutions at the PGC-1agr gene locus and their haplotype structure is discussed in relation to human disease phenotypes.

Keywords: coregulators; nuclear hormone receptors; mitochondrial biogenesis; energy metabolism

Document Type: Review article

DOI: 10.2174/1389202043349129

Affiliations: 1: Department of Laboratory Medicine, Landeskliniken Salzburg, A-5020 Salzburg, Austria.

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