A PGC-1α-O-GlcNAc transferase complex regulates FoxO transcription factor activity in response to glucose

Abstract

Metabolic and stress response gene regulation is crucial for the survival of an organism to a changing environment. Three key molecules that sense nutrients and broadly affect gene expression are the FoxO transcription factors, the transcriptional co-activator PGC-1α, and the dynamic post-translational modification, O-linked β-N-acetylglucosamine (O-GlcNAc). Here we identify novel post-translational modifications of PGC-1α, including O-GlcNAc, and describe a novel mechanism for how PGC-1α co-activates transcription by FoxOs. In liver, in cultured cells, and in vitro with recombinant proteins, PGC-1α binds to O-GlcNAc transferase and targets the enzyme to FoxOs, resulting in their increased GlcNAcylation and increased transcriptional activity. Furthermore, glucose-enhanced activation of FoxO1 occurs via this PGC-1α-O-GlcNAc transferase-mediated GlcNAcylation. Therefore, one mechanism by which PGC-1α can serve as a co-activator of transcription is by targeting the O-GlcNAc transferase to increase Glc-NAcylation of specific transcription factors important to nutrient/stress sensing and energy metabolism. © 2009 by The American Society for Biochemistry and Molecular Biology, Inc.