Gain-of-function mutations associated with hereditary pancreatitis enhance autoactivation of human cationic trypsinogen

Biochem Biophys Res Commun. 2000 Nov 19;278(2):286-9. doi: 10.1006/bbrc.2000.3797.


Hereditary pancreatitis (HP), an autosomal dominant disorder, has been associated with mutations in the cationic trypsinogen gene. Here we demonstrate that the two most frequent HP mutations, Arg117 --> His and Asn21 --> Ile, significantly enhance autoactivation of human cationic trypsinogen in vitro, in a manner that correlates with the severity of clinical symptoms in HP. In addition, mutation Arg117 --> His inhibits autocatalytic inactivation of trypsin, while mutation Asn21 --> Ile has no such effect. The findings strongly argue that increased trypsinogen activation in the pancreas is the common initiating step in both forms of HP, whereas trypsin stabilization might also contribute to HP associated with the Arg117 --> His mutation.

MeSH terms

  • Catalysis
  • Enteropeptidase / metabolism
  • Enzyme Activation
  • Humans
  • Mutation*
  • Pancreatitis / genetics*
  • Recombinant Proteins / metabolism
  • Trypsinogen / metabolism*


  • Recombinant Proteins
  • Trypsinogen
  • Enteropeptidase