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The energy sensor AMP-activated protein kinase directly regulates the mammalian FOXO3 transcription factor.

The maintenance of homeostasis throughout an organism's life span requires constant adaptation to changes in energy levels. The AMP-activated protein kinase (AMPK) plays a critical role in the cellular responses to low energy levels by switching off energy-consuming pathways and switching on energy-producing pathways. However, the transcriptional mechanisms by which AMPK acts to adjust cellular energy levels are not entirely characterized. Here, we find that AMPK directly regulates mammalian FOXO3, a member of the FOXO family of Forkhead transcription factors known to promote resistance to oxidative stress, tumor suppression, and longevity. We show that AMPK phosphorylates human FOXO3 at six previously unidentified regulatory sites. Phosphorylation by AMPK leads to the activation of FOXO3 transcriptional activity without affecting FOXO3 subcellular localization. Using a genome-wide microarray analysis, we identify a set of target genes that are regulated by FOXO3 when phosphorylated at these six regulatory sites in mammalian cells. The regulation of FOXO3 by AMPK may play a crucial role in fine tuning gene expression programs that control energy balance and stress resistance in cells throughout life.

Pubmed ID: 17711846 RIS Download

Mesh terms: AMP-Activated Protein Kinases | Amino Acid Sequence | Animals | Cell Line | Forkhead Box Protein O3 | Forkhead Transcription Factors | Gene Expression Regulation | Humans | Luciferases | Mass Spectrometry | Mice | Mice, Transgenic | Models, Biological | Molecular Sequence Data | Multienzyme Complexes | Phosphorylation | Protein-Serine-Threonine Kinases | Transcription, Genetic

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Associated grants

  • Agency: NCI NIH HHS, Id: T32 CA009302
  • Agency: NIA NIH HHS, Id: AG026648-01
  • Agency: NCI NIH HHS, Id: CA 09302

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