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Transcriptional control of brown fat determination by PRDM16.

Brown fat cells are specialized to dissipate energy and can counteract obesity; however, the transcriptional basis of their determination is largely unknown. We show here that the zinc-finger protein PRDM16 is highly enriched in brown fat cells compared to white fat cells. When expressed in white fat cell progenitors, PRDM16 activates a robust brown fat phenotype including induction of PGC-1alpha, UCP1, and type 2 deiodinase (Dio2) expression and a remarkable increase in uncoupled respiration. Transgenic expression of PRDM16 at physiological levels in white fat depots stimulates the formation of brown fat cells. Depletion of PRDM16 through shRNA expression in brown fat cells causes a near total loss of the brown characteristics. PRDM16 activates brown fat cell identity at least in part by simultaneously activating PGC-1alpha and PGC-1beta through direct protein binding. These data indicate that PRDM16 can control the determination of brown fat fate.

Pubmed ID: 17618855


  • Seale P
  • Kajimura S
  • Yang W
  • Chin S
  • Rohas LM
  • Uldry M
  • Tavernier G
  • Langin D
  • Spiegelman BM


Cell metabolism

Publication Data

July 9, 2007

Associated Grants

  • Agency: NIDDK NIH HHS, Id: DK31405-24
  • Agency: NIDDK NIH HHS, Id: R37 DK031405
  • Agency: NIDDK NIH HHS, Id: R37 DK031405-25

Mesh Terms

  • 3T3-L1 Cells
  • Adipocytes
  • Adipocytes, Brown
  • Adipocytes, White
  • Adipose Tissue, Brown
  • Adipose Tissue, White
  • Animals
  • Blotting, Western
  • COS Cells
  • Cell Differentiation
  • Cell Respiration
  • Cells, Cultured
  • Cercopithecus aethiops
  • DNA-Binding Proteins
  • Electrophoretic Mobility Shift Assay
  • Fibroblasts
  • Gene Expression Regulation
  • Genes, Reporter
  • Iodide Peroxidase
  • Ion Channels
  • Male
  • Mice
  • Mice, Inbred C3H
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Mice, Transgenic
  • Mitochondria
  • Mitochondrial Proteins
  • Oxygen Consumption
  • Phenotype
  • Reverse Transcriptase Polymerase Chain Reaction
  • Trans-Activators
  • Transcription Factors
  • Transcription, Genetic