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Noradrenergic neuronal development is impaired by mutation of the proneural HASH-1 gene in congenital central hypoventilation syndrome (Ondine's curse).

Congenital central hypoventilation syndrome (CCHS, Ondine's curse) is a rare disorder of the chemical control of breathing. It is frequently associated with a broad spectrum of dysautonomic symptoms, suggesting the involvement of genes widely expressed in the autonomic nervous system. In particular, the HASH-1-PHOX2A-PHOX2B developmental cascade was proposed as a candidate pathway because it controls the development of neurons with a definitive or transient noradrenergic phenotype, upstream from the RET receptor tyrosine kinase and tyrosine hydroxylase. We recently showed that PHOX2B is the major CCHS locus, whose mutation accounts for 60% of cases. We also studied the proneural HASH-1 gene and identified a heterozygous nucleotide substitution in three CCHS patients. To analyze the functional consequences of HASH-1 mutations, we developed an in vitro model of noradrenergic differentiation in neuronal progenitors derived from the mouse vagal neural crest, reproducing in vitro the HASH-PHOX-RET pathway. All HASH-1 mutant alleles impaired noradrenergic neuronal development, when overexpressed from adenoviral constructs. Thus, HASH-1 mutations may contribute to the CCHS phenotype in rare cases, consistent with the view that the abnormal chemical control of breathing observed in CCHS patients is due to the impairment of noradrenergic neurons during early steps of brainstem development.

Pubmed ID: 14532329


  • de Pontual L
  • Népote V
  • Attié-Bitach T
  • Al Halabiah H
  • Trang H
  • Elghouzzi V
  • Levacher B
  • Benihoud K
  • Augé J
  • Faure C
  • Laudier B
  • Vekemans M
  • Munnich A
  • Perricaudet M
  • Guillemot F
  • Gaultier C
  • Lyonnet S
  • Simonneau M
  • Amiel J


Human molecular genetics

Publication Data

December 1, 2003

Associated Grants


Mesh Terms

  • Alleles
  • Amino Acid Sequence
  • Animals
  • Basic Helix-Loop-Helix Transcription Factors
  • Cells, Cultured
  • DNA-Binding Proteins
  • Female
  • Gene Expression
  • Genetic Variation
  • Humans
  • Male
  • Mice
  • Molecular Sequence Data
  • Mutation
  • Phylogeny
  • Sequence Homology, Amino Acid
  • Sleep Apnea, Central
  • Transcription Factors