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The Ret(C620R) mutation affects renal and enteric development in a mouse model of Hirschsprung's disease.

In rare families RET tyrosine kinase receptor substitutions located in exon 10 (especially at positions 609, 618, and 620) can concomitantly cause the MEN 2A (multiple endocrine neoplasia type 2A) or FMTC (familial medullary thyroid carcinoma) cancer syndromes, and Hirschsprung's disease (HSCR). No animal model mimicking the co-existence of the MEN 2 pathology and HSCR is available, and the association of these activating mutations with a developmental defect still represents an unresolved problem. The aim of this work was to investigate the significance of the RET(C620R) substitution in the pathogenesis of both gain- and loss-of-function RET-associated diseases. We report the generation of a line of mice carrying the C620R mutation in the Ret gene. Although Ret(C620R) homozygotes display severe defects in kidney organogenesis and enteric nervous system development leading to perinatal lethality. Ret(C620R) heterozygotes recapitulate features characteristic of HSCR including hypoganglionosis of the gastrointestinal tract. Surprisingly, heterozygotes do not show any defects in the thyroid that might be attributable to a gain-of-function mutation. The Ret(C620R) allele is responsible for HSCR and affects the development of kidneys and the enteric nervous system (ENS). These mice represent an interesting model for studying new therapeutic approaches for the treatment of HSCR disease.

Pubmed ID: 16565500


  • Carniti C
  • Belluco S
  • Riccardi E
  • Cranston AN
  • Mondellini P
  • Ponder BA
  • Scanziani E
  • Pierotti MA
  • Bongarzone I


The American journal of pathology

Publication Data

April 27, 2006

Associated Grants

  • Agency: Telethon, Id: E.0993

Mesh Terms

  • Amino Acid Substitution
  • Animals
  • Cells, Cultured
  • Disease Models, Animal
  • Enteric Nervous System
  • Female
  • Ganglia, Spinal
  • Gastrointestinal Tract
  • Hirschsprung Disease
  • Kidney
  • Male
  • Mice
  • Mice, Mutant Strains
  • Proto-Oncogene Proteins c-ret
  • Thyroid Gland