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Modulation of PPAR activity via phosphorylation Burns KA; Vanden Heuvel JPBiochim Biophys Acta 2007[Aug]; 1771 (8): 952-60Peroxisome proliferator-activated receptors (PPARs) are members of the nuclear receptor superfamily of transcription factors that respond to specific ligands by altering gene expression in a cell-, developmental- and sex-specific manner. Three subtypes of this receptor have been discovered (PPARalpha, beta and gamma), each apparently evolving to fulfill different biological niches. PPARs control a variety of target genes involved in lipid homeostasis, diabetes and cancer. Similar to other nuclear receptors, the PPARs are phosphoproteins and their transcriptional activity is affected by cross-talk with kinases and phosphatases. Phosphorylation by the mitogen-activated protein kinases (ERK- and p38-MAPK), Protein Kinase A and C (PKA, PKC), AMP Kinase (AMPK) and glycogen synthase kinase-3 (GSK3) affect their activity in a ligand-dependent or -independent manner. The effects of phosphorylation depend on the cellular context, receptor subtype and residue metabolized which can be manifested at several steps in the PPAR activation sequence including ligand affinity, DNA binding, coactivator recruitment and proteasomal degradation. The review will summarize the known PPAR kinases that directly act on these receptors, the sites affected and the result of this modification on receptor activity.|Animals[MESH]|Cyclic AMP-Dependent Protein Kinases/metabolism[MESH]|Extracellular Signal-Regulated MAP Kinases/metabolism[MESH]|Growth Substances/physiology[MESH]|Humans[MESH]|Mitogen-Activated Protein Kinase Kinases/metabolism[MESH]|PPAR alpha/metabolism[MESH]|PPAR delta/metabolism[MESH]|PPAR gamma/metabolism[MESH]|PPAR-beta/metabolism[MESH]|Peroxisome Proliferator-Activated Receptors/*metabolism[MESH]|Phosphorylation[MESH]|Signal Transduction[MESH]|Transcription Factors/metabolism[MESH] |
