A major quantitative trait locus co-localizing with cholecystokinin type A receptor gene influences poor pancreatic proliferation in a spontaneously diabetogenic rat

Mamm Genome. 1998 Oct;9(10):794-8. doi: 10.1007/s003359900869.

Abstract

The Otsuka Long-Evans Tokushima Fatty (OLETF) rat is an animal model for obese-type, non-insulin-dependent diabetes mellitus (NIDDM) in humans. The OLETF rat has poor capacity for pancreatic proliferation, which may be the critical pathogenetic event in NIDDM development. Our investigation was designed to identify quantitative trait loci (QTLs) responsible for poor pancreatic proliferation by examining compensatory proliferation of the pancreatic remnant after partial pancreatectomy and performing a genome-wide scan in an F2 intercross obtained by mating the OLETF and the Fischer-344 (F344) rats. We identified a highly significant QTL on rat Chromosome 14 with a maximum lod score of 16.7, which accounts for 55% of the total variance. The QTL co-localizes with the gene encoding cholecystokinin type A receptor (CCKAR) which is likely to mediate the trophic effect of cholecystokinin on pancreas and is defective in the OLETF rat.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Division / genetics
  • Chromosome Mapping
  • Diabetes Mellitus, Type 2 / genetics*
  • Diabetes Mellitus, Type 2 / pathology*
  • Diabetes Mellitus, Type 2 / physiopathology
  • Female
  • Genetic Linkage
  • Genotype
  • Islets of Langerhans / pathology*
  • Islets of Langerhans / physiopathology
  • Male
  • Pancreatectomy
  • Phenotype
  • Quantitative Trait, Heritable*
  • Rats
  • Rats, Inbred F344
  • Rats, Inbred OLETF
  • Receptor, Cholecystokinin A
  • Receptors, Cholecystokinin / genetics*
  • Regeneration / genetics

Substances

  • Receptor, Cholecystokinin A
  • Receptors, Cholecystokinin