HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Progressive onset of adrenal insufficiency and hypogonadism of pituitary origin caused by a complex genetic rearrangement within DAX-1.

Abstract
DAX-1 [dosage-sensitive sex reversal, adrenal hypoplasia congenital (AHC) critical region on the X chromosome, gene 1] is a transcription factor expressed in the adrenal gland and at all levels of the gonadotrope axis. Inactivating mutations of DAX1 result in the X-linked form of AHC with associated hypogonadotropic hypogonadism. AHC usually reveals itself as adrenal failure in early infancy, although a wide range of phenotypic expression has been reported. We describe a patient who was diagnosed with adrenal failure at 6 wk of age, but who experienced recovery of adrenal function of several months' duration later in infancy. He subsequently failed to undergo puberty because of hypogonadotropic hypogonadism of pituitary origin, and he was also diagnosed with schizophrenia in early adulthood. Molecular genetic analyses revealed a complex rearrangement in DAX1, including a 2.2-kb deletion spanning the entire second exon and a small 27-bp insertion. The putative protein encoded by this mutated gene is 429 amino acids long. The initial 389 residues probably correspond to the wild-type DAX-1 sequence, whereas the last 40 amino acids are presumably completely unrelated, being transcribed from the intronic sequence adjacent to exon 1. In vitro functional analyses confirm the absence of repressor activity exerted by such mutant protein. These studies expand the genotypic and phenotypic spectrum of DAX-1 insufficiency in humans.
AuthorsRoberto Salvi, Fulgencio Gomez, Muriel Fiaux, Daniel Schorderet, J Larry Jameson, John C Achermann, Rolf C Gaillard, François P Pralong
JournalThe Journal of clinical endocrinology and metabolism (J Clin Endocrinol Metab) Vol. 87 Issue 9 Pg. 4094-100 (Sep 2002) ISSN: 0021-972X [Print] United States
PMID12213854 (Publication Type: Case Reports, Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S.)
Chemical References
  • DAX-1 Orphan Nuclear Receptor
  • DNA Primers
  • DNA-Binding Proteins
  • NR0B1 protein, human
  • Receptors, Retinoic Acid
  • Repressor Proteins
  • Transcription Factors
Topics
  • Adolescent
  • Adrenal Insufficiency (genetics, physiopathology)
  • Amino Acid Sequence
  • Base Sequence
  • Cells, Cultured
  • DAX-1 Orphan Nuclear Receptor
  • DNA Primers
  • DNA-Binding Proteins (genetics)
  • Disease Progression
  • Gene Rearrangement
  • Humans
  • Hypogonadism (genetics)
  • Hypopituitarism (genetics)
  • Male
  • Mutagenesis, Site-Directed
  • Polymerase Chain Reaction
  • Receptors, Retinoic Acid (genetics)
  • Repressor Proteins
  • Sequence Deletion
  • Transcription Factors (genetics)
  • Transfection

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: