Evolution of Trypsinogen Activation Peptides

Jian Min Chen, Zoltán Kukor, Cédric Le Maréchal, Miklós Tóth, Laurent Tsakiris, Odile Raguénès, Claude Férec, Miklós Sahin-Tóth

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87 Citations (Scopus)

Abstract

The activation peptide of mammalian trypsinogens contains a highly conserved tetra-aspartate sequence (D19-D20-D21-D22) preceding the K23-I24 scissile peptide bond, which is hydrolyzed as the first step in the activation process. Here, we examined the evolution and function of trypsinogen activation peptides through integrating functional characterization of disease-associated mutations with comparative genomic analysis. Activation properties of three chronic pancreatitis-associated activation peptide mutants (the novel D19A and the previously reported D22G and K23R) were simultaneously analyzed, for the first time, in the context of recombinant human cationic trypsinogen. A dramatic increase in autoactivation of cationic trypsinogen was observed in all three mutants, with D22G and K23R exhibiting the most marked increases. The physiological activator enteropeptidase activated the D19A mutant normally, activated the D22G mutant very poorly, and stimulated activation of the K23R mutant. The biochemical and structural data, taken together with a comprehensive sequence comparison, indicates that the tetra-aspartate sequence in mammalian trypsinogen activation peptides has evolved not only for optimal enteropeptidase recognition in the duodenum but also for efficient inhibition of trypsinogen autoactivation within the pancreas. Moreover, the use of lysine instead of arginine at the P1 position of activation peptides also has an advantageous effect against trypsinogen autoactivation. Finally, fixed substitutions in the key residues of the trypsinogen activation peptide may suggest the evolution of new functions unrelated to digestion, as found in the group III trypsinogens of cold-adapted fishes.

Original languageEnglish
Pages (from-to)1767-1777
Number of pages11
JournalMolecular biology and evolution
Volume20
Issue number11
DOIs
Publication statusPublished - Nov 1 2003

Keywords

  • Activation peptide
  • Chronic pancreatitis
  • Comparative genomic analysis
  • Human cationic trypsinogen
  • Missense mutation
  • Molecular evolution

ASJC Scopus subject areas

  • Ecology, Evolution, Behavior and Systematics
  • Molecular Biology
  • Genetics

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  • Cite this

    Chen, J. M., Kukor, Z., Le Maréchal, C., Tóth, M., Tsakiris, L., Raguénès, O., Férec, C., & Sahin-Tóth, M. (2003). Evolution of Trypsinogen Activation Peptides. Molecular biology and evolution, 20(11), 1767-1777. https://doi.org/10.1093/molbev/msg183