Amino-terminal region of human macrophage colony-stimulating factor (M-CSF) is sufficient for its in vitro biological activity: molecular cloning and expression of carboxyl-terminal deletion mutants of human M-CSF

Biochem Biophys Res Commun. 1989 Jun 15;161(2):892-901. doi: 10.1016/0006-291x(89)92683-1.

Abstract

Human T lymphoblastoid cell line CEM-ON belongs to a helper/inducer subclass and secretes M-CSF into medium constitutively. We have isolated a full-length cDNA clone for this factor from a cDNA library of this cell line. The cDNA was 2.5 kb and coded for a 554 amino acid polypeptide precursor including signal sequence. The Northern blot analysis showed that the major transcript of M-CSF is about 4.2 kb. We have studied the expression of not only the wild type plasmid, but also the five C-terminal deletion mutants encoding N-terminal 154, 163, 170, 177, and 185 amino acid residues in monkey COS-1 cells. The results showed that at least C-terminal 377 amino acid residues of human M-CSF are not essential to manifest the in vitro biological activity on murine bone marrow cells.

MeSH terms

  • Amino Acid Sequence
  • Base Sequence
  • Blotting, Northern
  • Chromosome Deletion
  • Cloning, Molecular
  • Colony-Stimulating Factors / genetics
  • Colony-Stimulating Factors / pharmacology*
  • DNA Mutational Analysis
  • Humans
  • Macrophage Colony-Stimulating Factor
  • Molecular Sequence Data
  • Recombinant Proteins / pharmacology
  • Structure-Activity Relationship

Substances

  • Colony-Stimulating Factors
  • Recombinant Proteins
  • Macrophage Colony-Stimulating Factor

Associated data

  • GENBANK/M27087