Reduced body weight gain in ubiquilin-1 transgenic mice is associated with increased expression of energy-sensing proteins

Physiol Rep. 2017 Apr;5(8):e13260. doi: 10.14814/phy2.13260.

Abstract

Ubiquilin-1 (Ubqln1), a ubiquitin-like protein, is implicated in a variety of pathophysiological processes, but its role in mediating body weight gain or metabolism has not been determined. Here, we demonstrate that global overexpression of Ubqln1 in a transgenic (Tg) mouse reduces the animal's body weight gain. The decreased body weight gain in Tg mice is associated with lower visceral fat content and higher metabolic rate. The Ubqln1 Tg mice exhibited reduced leptin and insulin levels as well as increased insulin sensitivity manifested by homeostatic model assessment of insulin resistance. Additionally, the reduced body weight in Tg mice was associated with the upregulation of two energy-sensing proteins, sirtuin1 (SIRT1) in the hypothalamus and AMP-activated protein kinase (AMPK) in the skeletal muscle. Consistent with the in vivo results, overexpression of Ubqln1 significantly increased SIRT1 and AMPK levels in the mouse embryonic fibroblast cell culture. Thus, our results not only establish the link between Ubqln1 and body weight regulation but also indicate that the metabolic function of Ubqln1 on body weight may be through regulating energy-sensing proteins.

Keywords: Body weight; energy‐sensing proteins; mice; ubiquilin‐1.

MeSH terms

  • AMP-Activated Protein Kinase Kinases
  • Adaptor Proteins, Signal Transducing
  • Adaptor Proteins, Vesicular Transport / genetics*
  • Adaptor Proteins, Vesicular Transport / metabolism
  • Animals
  • Autophagy-Related Proteins
  • Cells, Cultured
  • Female
  • Fibroblasts / metabolism
  • Hypothalamus / metabolism
  • Insulin / blood
  • Insulin Resistance
  • Intra-Abdominal Fat / growth & development
  • Intra-Abdominal Fat / metabolism
  • Leptin / blood
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Muscle, Skeletal / metabolism
  • Protein Kinases / genetics
  • Protein Kinases / metabolism*
  • Sirtuin 1 / genetics
  • Sirtuin 1 / metabolism*
  • Thinness / genetics*
  • Thinness / metabolism

Substances

  • Adaptor Proteins, Signal Transducing
  • Adaptor Proteins, Vesicular Transport
  • Autophagy-Related Proteins
  • Insulin
  • Leptin
  • UBQLN1 protein, mouse
  • Protein Kinases
  • AMP-Activated Protein Kinase Kinases
  • Sirt1 protein, mouse
  • Sirtuin 1