PGC-1
: 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-1
, originally described as transcriptional coactivator of PPAR
, has since been shown to act in a much broader context. PGC-1
coordinates the transcriptional programs of several key cellular pathways including mitochondrial biogenesis, thermogenesis, hepatic gluconeogenesis and
- oxidation of fatty acids via interactions with a growing number of transcription factors. A central issue to understand the diverse functions of PGC-1
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-1
function and the implications for tissue and context-specific transcriptional responses. Moreover, the role of sequence substitutions at the PGC-1
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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