
pmid: 14636573
Transcriptional coactivators showing physical and functional interactions with PPARgamma include the protein acetyl transferase p300, the TRAP/Mediator complex that interacts with the general transcription machinery, and the highly regulated PGC-1alpha. We show that PGC-1alpha directly interacts with TRAP/Mediator, through the PPARgamma-interacting subunit TRAP220, and stimulates TRAP/Mediator-dependent function on DNA templates. Further, while ineffective by itself, PGC-1alpha stimulates p300-dependent histone acetylation and transcription on chromatin templates in response to PPARgamma. These functions are mediated by largely independent PPARgamma, p300, and TRAP220 interaction domains in PGC-1alpha, whereas p300 and TRAP220 show ligand-dependent interactions with a common region of PPARgamma. Apart from showing PGC-1alpha functions both in chromatin remodeling and in preinitiation complex formation or function (transcription), these results suggest a key role for PGC-1alpha, through concerted but dynamic interactions, in coordinating these steps.
Mediator Complex, Transcription, Genetic, Recombinant Fusion Proteins, Nuclear Proteins, Receptors, Cytoplasmic and Nuclear, Cell Biology, Chromatin, Mediator Complex Subunit 1, Mice, Protein Subunits, Genes, Reporter, Trans-Activators, Animals, Humans, Molecular Biology, E1A-Associated p300 Protein, HeLa Cells, Transcription Factors
Mediator Complex, Transcription, Genetic, Recombinant Fusion Proteins, Nuclear Proteins, Receptors, Cytoplasmic and Nuclear, Cell Biology, Chromatin, Mediator Complex Subunit 1, Mice, Protein Subunits, Genes, Reporter, Trans-Activators, Animals, Humans, Molecular Biology, E1A-Associated p300 Protein, HeLa Cells, Transcription Factors
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