Functional interaction of bZIP proteins and the large subunit of replication factor C in liver and adipose cells

J Biol Chem. 2001 Jul 27;276(30):28098-105. doi: 10.1074/jbc.M010912200. Epub 2001 May 16.

Abstract

The transcription factor CCAAT/enhancer-binding protein-alpha (C/EBPalpha) has a vital role in cell growth and differentiation. To delineate further a mechanism for C/EBPalpha-mediated differentiation, we screened C/EBPalpha-interacting proteins through far-Western screening. One of the strongest interactions was with RFC140, the large subunit of the replication factor C complex. C/EBPalpha specifically interacted with RFC140 from rat liver nuclear extract as determined by a combination of affinity chromatography and co-immunoprecipitation. Subsequent far-Western blotting showed that the bZIP domain of C/EBPalpha interacted with the DNA-binding region of RFC140. Overexpression of RFC140 in mammalian cells increased the transactivation activity of C/EBPalpha on both minimal and native promoters. Consistent with the enhanced transactivation, a complex of C/EBPalpha and RFC140 proteins with the cognate DNA element was detected in vitro. The specific interaction between C/EBPalpha and RFC140 was detected in the terminal differentiation of 3T3-L1 preadipocytes to adipocytes. The synergistic transcription effect of these two proteins increased the promoter activity and protein expression of peroxisome proliferator-activated receptor-gamma, which is a main regulator of adipocyte differentiation. Our results demonstrate that the specific transcription factor C/EBPalpha and the general DNA replication factor RFC140 interact functionally and physically. This observation highlights a unique mechanism by which the levels of the general replication factor can strongly modulate the functional activity of the specific transcription factor as a coactivator.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipocytes / metabolism
  • Adipose Tissue / cytology
  • Adipose Tissue / metabolism*
  • Animals
  • Blotting, Western
  • Cell Differentiation
  • Chromatography, Affinity
  • Cloning, Molecular
  • DNA / metabolism
  • DNA, Complementary / metabolism
  • DNA-Binding Proteins / chemistry*
  • Fibroblasts / metabolism
  • Glutathione Transferase / metabolism
  • Liver / metabolism*
  • Mice
  • Nuclear Proteins*
  • Precipitin Tests
  • Protein Binding
  • Protein Structure, Tertiary
  • RNA-Binding Proteins*
  • Rats
  • Receptors, Cytoplasmic and Nuclear / metabolism
  • Recombinant Fusion Proteins / metabolism
  • Replication Protein C
  • Transcription Factors / chemistry*
  • Transcription Factors / metabolism
  • Transcription, Genetic
  • Transcriptional Activation
  • Transfection

Substances

  • DNA, Complementary
  • DNA-Binding Proteins
  • Nuclear Proteins
  • RNA-Binding Proteins
  • Receptors, Cytoplasmic and Nuclear
  • Recombinant Fusion Proteins
  • Refbp1 protein, mouse
  • Transcription Factors
  • DNA
  • Glutathione Transferase
  • Replication Protein C