C/EBP, c-Myb, and PU.1 cooperate to regulate the neutrophil elastase promoter

Mol Cell Biol. 1996 Sep;16(9):4717-25. doi: 10.1128/MCB.16.9.4717.

Abstract

The murine neutrophil elastase (NE) gene is expressed specifically in immature myeloid cells. A 91-bp NE promoter region contains three cis elements which are conserved evolutionarily and are essential for activation of the promoter in differentiating 32D cl3 myeloid cells. These elements bound c-Myb (at -49), C/EBPalpha (at -57), and PU.1 (at -82). In NIH 3T3 cells, the NE promoter was activated by c-Myb, C/EBPalpha, and PU.1, via their respective binding sites. Cooperative activation was seen by any combination of c-Myb, C/EBPalpha, and PU.1, including all three together, again via their DNA-binding sites. In CV-1 cells, but not in NIH 3T3 cells, cooperation between Myb and C/EBPalpha depended on the integrity of the PU.1-binding site. In addition to C/EBPalpha, C/EBPdelta strongly activated the NE promoter, alone or with c-Myb, but C/EBPbeta was less active. Either of C/EBPalpha's two transactivation domains cooperatively activated the promoter with c-Myb, in both NIH 3T3 and 32D c13 cells. Synergistic binding to DNA in a gel shift assay between C/EBPalpha, c-Myb, and PU.1 could not be demonstrated. Also, separation of the C/EBP- and c-Myb-binding sites by 5 or 10 bp did not prevent cooperativity. These results suggest that a coactivator protein mediates cooperative activation of the NE promoter by a C/EBP and c-Myb. These factors, together with PU.1, direct restricted expression of the NE promoter to immature myeloid cells.

Publication types

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

MeSH terms

  • 3T3 Cells
  • Animals
  • Base Sequence
  • CCAAT-Enhancer-Binding Proteins
  • Cell Differentiation
  • Cell Line
  • Chlorocebus aethiops
  • DNA / metabolism
  • DNA-Binding Proteins / pharmacology
  • DNA-Binding Proteins / physiology*
  • Drug Synergism
  • Enzyme Induction
  • Hematopoietic Stem Cells
  • Leukocyte Elastase
  • Macromolecular Substances
  • Mice
  • Molecular Sequence Data
  • Nuclear Proteins / pharmacology
  • Nuclear Proteins / physiology*
  • Pancreatic Elastase / biosynthesis
  • Pancreatic Elastase / genetics*
  • Protein Binding
  • Proto-Oncogene Proteins / pharmacology
  • Proto-Oncogene Proteins / physiology*
  • Proto-Oncogene Proteins c-myb
  • Recombinant Fusion Proteins / pharmacology
  • Regulatory Sequences, Nucleic Acid
  • Trans-Activators / pharmacology
  • Trans-Activators / physiology*
  • Transcriptional Activation

Substances

  • CCAAT-Enhancer-Binding Proteins
  • DNA-Binding Proteins
  • Macromolecular Substances
  • Nuclear Proteins
  • Proto-Oncogene Proteins
  • Proto-Oncogene Proteins c-myb
  • Recombinant Fusion Proteins
  • Trans-Activators
  • proto-oncogene protein Spi-1
  • DNA
  • Pancreatic Elastase
  • Leukocyte Elastase