Upregulation of Tribbles decreases body weight and increases sleep duration

Dis Model Mech. 2023 Apr 1;16(4):dmm049942. doi: 10.1242/dmm.049942. Epub 2023 Apr 21.

Abstract

Eukaryotic Tribbles proteins are pseudoenzymes that regulate multiple aspects of intracellular signalling. Both Drosophila melanogaster and mammalian members of this family of pseudokinases act as negative regulators of insulin signalling. Mammalian tribbles pseudokinase (TRIB) genes have also been linked to insulin resistance and type 2 diabetes mellitus. Type 2 diabetes mellitus is associated with increased body weight, sleep problems and increased long-term mortality. Here, we investigated how manipulating the expression of Tribbles impacts body weight, sleep and mortality. We showed that the overexpression of Drosophila tribbles (trbl) in the fly fat body reduces both body weight and lifespan in adult flies without affecting food intake. Furthermore, it decreases the levels of Drosophila insulin-like peptide 2 (DILP2; ILP2) and increases night-time sleep. The three genes encoding TRIBs of mammals, TRIB1, TRIB2 and TRIB3, show both common and unique features. As the three human TRIB genes share features with Drosophila trbl, we further explored the links between TRIB genetic variants and both body weight and sleep in the human population. We identified associations between the polymorphisms and expression levels of the pseudokinases and markers of body weight and sleep duration. We conclude that Tribbles pseudokinases are involved in the control of body weight, lifespan and sleep.

Keywords: Drosophila; Fat body; Lifespan; Lipid metabolism; Sleep; Tribbles.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Body Weight
  • Calcium-Calmodulin-Dependent Protein Kinases / genetics
  • Calcium-Calmodulin-Dependent Protein Kinases / metabolism
  • Cell Cycle Proteins / genetics
  • Diabetes Mellitus, Type 2*
  • Drosophila melanogaster / genetics
  • Drosophila melanogaster / metabolism
  • Humans
  • Insulin / metabolism
  • Intracellular Signaling Peptides and Proteins / genetics
  • Intracellular Signaling Peptides and Proteins / metabolism
  • Mammals / metabolism
  • Neuropeptides*
  • Protein Serine-Threonine Kinases / genetics
  • Protein Serine-Threonine Kinases / metabolism
  • Sleep Duration
  • Up-Regulation / genetics

Substances

  • Calcium-Calmodulin-Dependent Protein Kinases
  • Cell Cycle Proteins
  • ILP2 protein, Drosophila
  • Insulin
  • Intracellular Signaling Peptides and Proteins
  • Neuropeptides
  • Protein Serine-Threonine Kinases
  • TRIB1 protein, human
  • TRIB2 protein, human
  • trbl protein, Drosophila
  • TRIB3 protein, human