DEF-1, a novel Src SH3 binding protein that promotes adipogenesis in fibroblastic cell lines

Mol Cell Biol. 1999 Mar;19(3):2330-7. doi: 10.1128/MCB.19.3.2330.

Abstract

The Src homology 3 (SH3) motif is found in numerous signal transduction proteins involved in cellular growth and differentiation. We have purified and cloned a novel protein, DEF-1 (differentiation-enhancing factor), from bovine brain by using a Src SH3 affinity column. Ectopic expression of DEF-1 in fibroblasts resulted in the differentiation of a significant fraction of the culture into adipocytes. This phenotype appears to be related to the induction of the transcription factor peroxisome proliferator-activated receptor gamma (PPARgamma), since DEF-1 NIH 3T3 cells demonstrated augmented levels of PPARgamma mRNA and, when treated with activating PPARgamma ligands, efficient induction of differentiation. Further evidence for a role for DEF-1 in adipogenesis was provided by heightened expression of DEF-1 mRNA in adipose tissue isolated from obese and diabetes mice compared to that in tissue isolated from wild-type mice. However, DEF-1 mRNA was detected in multiple tissues, suggesting that the signal transduction pathway(s) in which DEF-1 is involved is not limited to adipogenesis. These results suggest that DEF-1 is an important component of a signal transduction process that is involved in the differentiation of fibroblasts and possibly of other types of cells.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • 3T3 Cells
  • Adaptor Proteins, Signal Transducing*
  • Adipocytes / cytology*
  • Amino Acid Sequence
  • Animals
  • Base Sequence
  • Carrier Proteins / genetics
  • Carrier Proteins / physiology*
  • Cattle
  • Cell Differentiation*
  • Cloning, Molecular
  • DNA, Complementary
  • Disease Models, Animal
  • Fibroblasts / cytology
  • Mice
  • Mice, Inbred BALB C
  • Molecular Sequence Data
  • Obesity
  • Rabbits
  • Receptors, Cytoplasmic and Nuclear / metabolism
  • Signal Transduction
  • Transcription Factors / metabolism
  • src Homology Domains*

Substances

  • ASAP1 protein, human
  • Adaptor Proteins, Signal Transducing
  • Asap1 protein, mouse
  • Carrier Proteins
  • DNA, Complementary
  • Receptors, Cytoplasmic and Nuclear
  • Transcription Factors

Associated data

  • GENBANK/AF112886