High-resolution dynamics of the transcriptional response to nutrition in Drosophila: a key role for dFOXO

Physiol Genomics. 2007 Mar 14;29(1):24-34. doi: 10.1152/physiolgenomics.00061.2006. Epub 2006 Nov 7.

Abstract

A high-resolution time series of transcript abundance was generated to describe global expression dynamics in response to nutrition in Drosophila. Nonparametric change-point statistics revealed that within 7 h of feeding upon yeast, transcript levels changed significantly for approximately 3,500 genes or 20% of the Drosophila genome. Differences as small as 15% were highly significant, and 80% of the changes were <1.5-fold. Notably, transcript changes reflected rapid downregulation of the nutrient-sensing insulin and target of rapamycin pathways, shifting of fuel metabolism from lipid to glucose oxidation, and increased purine synthesis, TCA-biosynthetic functions and mitochondria biogenesis. To investigate how nutrition coordinates these transcriptional changes, feeding-induced expression changes were compared with those induced by the insulin-regulated transcription factor dFOXO in Drosophila S2 cells. Remarkably, 28% (995) of the nutrient-responsive genes were regulated by activated dFOXO, including genes of mitochondrial biogenesis and a novel homolog of mammalian peroxisome proliferator-gamma coactivator-1 (PGC-1), a transcriptional coactivator implicated in controlling mitochondrial gene expression in mammals. These data implicate dFOXO as a major coordinator of the transcriptional response to nutrients downstream of insulin and suggest that mitochondria biogenesis is linked to insulin signaling via dFOXO-mediated repression of a PGC-1 homolog.

Publication types

  • Comparative Study
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animal Nutritional Physiological Phenomena / physiology*
  • Animals
  • Cells, Cultured
  • Drosophila Proteins / metabolism*
  • Drosophila Proteins / pharmacology
  • Drosophila melanogaster / metabolism
  • Drosophila melanogaster / physiology*
  • Energy Metabolism / physiology
  • Female
  • Forkhead Transcription Factors / metabolism*
  • Forkhead Transcription Factors / pharmacology
  • Gene Expression Profiling
  • Gene Expression Regulation / drug effects
  • Gene Expression Regulation / physiology*
  • Insulin / metabolism
  • Mitochondrial Proteins / metabolism
  • Time Factors
  • Transcription Factors / metabolism
  • Yeasts

Substances

  • Drosophila Proteins
  • FOXO protein, Drosophila
  • Forkhead Transcription Factors
  • Insulin
  • Mitochondrial Proteins
  • Transcription Factors
  • peroxisome-proliferator-activated receptor-gamma coactivator-1