GADD45γ regulates the thermogenic capacity of brown adipose tissue

Proc Natl Acad Sci U S A. 2014 Aug 12;111(32):11870-5. doi: 10.1073/pnas.1406638111. Epub 2014 Jul 28.

Abstract

The coactivator peroxisome proliferator-activated receptor-gamma coactivator 1 α (PGC-1α) is widely considered a central transcriptional regulator of adaptive thermogenesis in brown adipose tissue (BAT). However, mice lacking PGC-1α specifically in adipose tissue have only mild thermogenic defects, suggesting the presence of additional regulators. Using the activity of estrogen-related receptors (ERRs), downstream effectors of PGC-1α, as read-out in a high-throughput genome-wide cDNA screen, we identify here growth arrest and DNA-damage-inducible protein 45 γ (GADD45γ) as a cold-induced activator of uncoupling protein 1 (UCP1) and oxidative capacity in BAT. Mice lacking Gadd45γ have defects in Ucp1 induction and the thermogenic response to cold. GADD45γ works by activating MAPK p38, which is a potent activator of ERRβ and ERRγ transcriptional function. GADD45γ activates ERRγ independently of PGC-1 coactivators, yet synergizes with PGC-1α to induce the thermogenic program. Our findings elucidate a previously unidentified GADD45γ/p38/ERRγ pathway that regulates BAT thermogenesis and may enable new approaches for the stimulation of energy expenditure. Our study also implicates GADD45 proteins as general metabolic regulators.

Keywords: adrenergic response; norepinephrine signaling; nuclear receptors; transcriptional regulation.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Acclimatization / genetics
  • Acclimatization / physiology
  • Adipose Tissue, Brown / physiology*
  • Animals
  • Carrier Proteins / genetics
  • Carrier Proteins / metabolism*
  • Cells, Cultured
  • Cold Temperature
  • Energy Metabolism
  • Female
  • Gene Expression
  • Intracellular Signaling Peptides and Proteins
  • Ion Channels / biosynthesis
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Mitochondrial Proteins / biosynthesis
  • Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha
  • Receptors, Estrogen / metabolism
  • Signal Transduction
  • Thermogenesis / genetics
  • Thermogenesis / physiology*
  • Transcription Factors / metabolism
  • Uncoupling Protein 1
  • p38 Mitogen-Activated Protein Kinases / metabolism

Substances

  • Carrier Proteins
  • Esrrb protein, mouse
  • Esrrg protein, mouse
  • Gadd45g protein, mouse
  • Intracellular Signaling Peptides and Proteins
  • Ion Channels
  • Mitochondrial Proteins
  • Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha
  • Ppargc1a protein, mouse
  • Receptors, Estrogen
  • Transcription Factors
  • Ucp1 protein, mouse
  • Uncoupling Protein 1
  • p38 Mitogen-Activated Protein Kinases