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. 1997 Oct;41(4):436–441. doi: 10.1136/gut.41.4.436

Hirschsprung's disease: genetic mutations in mice and men

K ROBERTSON 1, I MASON 1, S HALL 1
PMCID: PMC1891517  PMID: 9391239

Abstract

MRC Brain Development Programme,Department of Developmental Neurobiology,UMDS Guy's Hospital,London SE1 9RT, UK

S HALL

Hirschsprung's disease is a neuronal dysplasia of the hindgut, characterised by a loss of neurones, which affects about 1in 5000 live births.1 Genetic factors have been implicated in the aetiology of this disease in about 20% of cases and a dominant pattern of inheritance has been revealed in several families. The pathogenesis of the aganglionosis is often attributed to a failure of migration of neural crest cells, although this has not been proven. 
Recently, mutations in a developmentally regulated receptor tyrosine kinase gene, ret, and mutations in the endothelin receptor-B gene (ENDR-B) have both been linked to familial Hirschsprung's disease in humans.4-6 Moreover, certain mutant mouse strains—namely piebald lethal and lethal spotted—exhibit striking similarities to the human condition. The mutation which gives rise to piebald lethal has now been found to be in the ENDR-B gene,7 and the mutation associated with lethal spotted occurs in the gene for endothelin-3 (ET-3), a ligand for ENDR-B.8 
Two transgenic mouse lines have been developed which also reflect the human disease: ret-k , which has a loss of function mutation of the ret gene,9 and ENDR-B null.10 In addition, the introduction of a Lac-Z reporter gene into neural crest cells of aganglionic mice has made it possible to study directly the fate of enteric neuroblasts which are affected by "Hirschsprung's-like" mutations.11 Here, we review the possible roles of RET and endothelin in the normal development of the enteric nervous system, and the significance of their mutated forms in the pathogenesis of familial aganglionosis. 
This review focuses on recent advances in our understanding of the genetic basis of the lesions which have been implicated in congenital forms of Hirschsprung's disease. Disruption of these genes in the mouse, either by transgenic "knockout" approaches or in mutant mouse lines, offers the prospect of greater understanding of both the cellular and developmental bases of the human disease. 



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Figure 1 .

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: (A) In situ hybridisation of chicken ret to a 10 somite stage chicken embryo. ret RNA is expressed in the vagal region of the neural ectoderm, (between the arrows), just prior to neural crest migration. The posterior region (S) of the neural ectoderm does not express ret. (B) and (C) In situ hybridisation of chicken ret to transverse sections through developing chicken mid-gut. (B) At embryonic day 4, ret positive neural crest derived precursors (arrowheads) are begining to migrate through the gut (D, dorsal; V, ventral). (C) At embryonic day 9, ret positive neuroblasts (arrowheads) have become organised into the myenteric (MY) and submucous (SM) plexuses. Reproduced from reference 30 with kind permission from Elsevier Science Ireland Ltd., Bay 15K, Shannon Industrial Estate, Co. Clare, Ireland. 


Selected References

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