Processing of mammalian preprogastrin-releasing peptide

Ann N Y Acad Sci. 1988:547:21-9. doi: 10.1111/j.1749-6632.1988.tb23872.x.

Abstract

The processing of preprogastrin-releasing peptide in mammalian tissues and in cultured cells takes place at discrete sites (Figure 6). Signal peptidase cleaves away the signal peptide from the amino terminus of gastrin-releasing peptide. An exopeptidase activity may remove dipeptides from the amino terminus. The amidation site (not shown in Fig. 6; see Fig. 2) has the same general sequence (Gly-Lys-Lys) seen for other amidated peptides. Cleavage after single basic residues yields gene-related products from Form I or II preproGRP. A unique non-basic cleavage yields a gene-related product from Form III preproGRP. The processing that occurs to form GRP, GRP, and GRP gene-related peptides is shown in Figure 7. ProGRP is cleaved by a series of enzymes to form GRP with an amidated carboxyl-terminal methionine (indicated by an asterisk in Fig. 7). GRP is cleaved to form the decapeptide GRP. The carboxyl-terminal flanking peptides of all three mRNA translation products are cleaved to form several gastrin-releasing peptide gene-related products. Knowledge of the processing of gastrin-releasing peptide and its gene-related products will allow synthesis of duplicates of the stored forms of these peptides, which can then be used for biological testing.

Publication types

  • Review

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Bombesin / genetics
  • Humans
  • Mammals
  • Molecular Sequence Data
  • Peptides / genetics*
  • Protein Precursors / genetics*
  • Protein Processing, Post-Translational*

Substances

  • Peptides
  • Protein Precursors
  • gastrin-releasing peptide precursor
  • Bombesin