Drosophila glucome screening identifies Ck1alpha as a regulator of mammalian glucose metabolism

Nat Commun. 2015 May 21:6:7102. doi: 10.1038/ncomms8102.

Abstract

Circulating carbohydrates are an essential energy source, perturbations in which are pathognomonic of various diseases, diabetes being the most prevalent. Yet many of the genes underlying diabetes and its characteristic hyperglycaemia remain elusive. Here we use physiological and genetic interrogations in D. melanogaster to uncover the 'glucome', the complete set of genes involved in glucose regulation in flies. Partial genomic screens of ∼1,000 genes yield ∼160 hyperglycaemia 'flyabetes' candidates that we classify using fat body- and muscle-specific knockdown and biochemical assays. The results highlight the minor glucose fraction as a physiological indicator of metabolism in Drosophila. The hits uncovered in our screen may have conserved functions in mammalian glucose homeostasis, as heterozygous and homozygous mutants of Ck1alpha in the murine adipose lineage, develop diabetes. Our findings demonstrate that glucose has a role in fly biology and that genetic screenings carried out in flies may increase our understanding of mammalian pathophysiology.

Publication types

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

MeSH terms

  • Adipose Tissue / metabolism*
  • Animals
  • Carbohydrate Metabolism
  • Casein Kinase I / genetics
  • Casein Kinase I / metabolism*
  • Drosophila melanogaster / genetics*
  • Fat Body / metabolism
  • Female
  • Gene-Environment Interaction
  • Glucose / metabolism*
  • Hemolymph / metabolism
  • Hyperglycemia / genetics*
  • Male
  • Metabolome
  • Mice
  • Muscles / enzymology
  • Mutation
  • Receptors, Cytoplasmic and Nuclear / metabolism
  • Transcription Factors / metabolism
  • Trehalose / metabolism

Substances

  • Receptors, Cytoplasmic and Nuclear
  • Transcription Factors
  • Trehalose
  • Casein Kinase I
  • Glucose