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Generation of truncated C/EBP beta isoforms by in vitro proteolysis

  1. Author:
    Baer, M.
    Johnson, P. F.

  2. Author Address

    Johnson PF NCI, Frederick Canc Res & Dev Ctr, Regulat Cell Growth Lab Frederick, MD 21702 USA NCI, Frederick Canc Res & Dev Ctr, Eukaryot Transcript Regulat Sect, Adv BioSci Labs,Basic Res Program Frederick, MD 21702 USA
    1. Year: 2000
  2. Journal: Journal of Biological Chemistry
    1. 275
    2. 34
    3. Pages: 26582-26590
  4. Type of Article: Article
  1. Abstract:

    Multiple forms of the transcriptional regulator CCAAT/enhancer-binding protein beta (C/EBP beta) with molecular masses of approximately 38, 34, 20, and 14 kDa have been observed in cell extracts. It has been proposed that these proteins arise by alternative initiation at in-frame AUG codons. The truncated C/EBP beta isoforms (p14 and p20/LIP) lack transactivation domains but retain DNA-binding and dimerization sequences and are therefore assumed to function as competitive inhibitors of C/EBP-mediated transcription in vivo. By comparing various extraction procedures to analyze endogenous and overexpressed C/EBP beta proteins, we determined that p20-C/EBP beta is generated predominantly by in vitro proteolytic cleavage during isolation from cells and that p14-C/EBP beta is produced exclusively by this mechanism. In transfected cells, the full-length (p34 and p38) isoforms but not the truncated proteins were detectable in the cytoplasm, indicating that the latter are not primary translation products. In addition, the C/EBP beta leucine zipper dimerization domain was essential for the appearance of the truncated species, demonstrating that protein folding or dimerization are critical determinants of proteolytic sensitivity. Our findings suggest that the presence of truncated C/EBP beta proteins in cell extracts must be interpreted with caution and that assumptions about the in vivo relevance of these isoforms should be re-evaluated. [References: 37]

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