RRC ID 19635
Author Goto M, Katsumata N.
Title X-linked adrenal hypoplasia congenita caused by a novel intronic mutation of the DAX-1 gene.
Journal Horm. Res.
Abstract OBJECTIVE:X-linked adrenal hypoplasia congenita (AHC) associated with hypogonadotropic hypogonadism (HHG) is caused by mutations of the DAX-1 gene. A novel intronic mutation of the gene and the results of in vitro expression analysis are reported.
PATIENT AND METHODS:The patient is a 13-year-old boy who presented with severe dehydration and salt loss in the neonatal period, when he lacked cutaneous pigmentation and elevation of plasma ACTH level. He had been diagnosed and treated as adrenal hypoplasia. The DAX-1 gene was analyzed by direct DNA sequencing in the patient and his parents. In vitro expression analysis was applied to confirm the consequent missplicing of mRNA caused by the mutation.
RESULTS:The substitution of guanine for cytosine at the splice donor site (IVS1 + 1G>C) was observed in our patient and his mother. Expression analysis suggested that this mutation may hinder splicing of the adjacent intron and cause alternative activation of three cryptic splice donor sites within exon 1 leading to the aberrant splicing of mRNA and production of truncated proteins.
CONCLUSION:To our knowledge, this is the first case report of AHC associated with HHG caused by an intronic mutation of the DAX-1 gene. The clinical course of our patient may suggest that the onset of mineralocorticoid deficiency can precede that of glucocorticoid deficiency in some patients with AHC, and thus appear to suffer from aldosterone synthase deficiency at the onset of the disease.
Volume 71(2)
Pages 120-4
Published 2009
DOI 10.1159/000183901
PII 000183901
PMID 19129717
MeSH Adolescent Adrenal Gland Diseases / genetics* Adrenal Gland Diseases / metabolism Adrenocorticotropic Hormone / metabolism Adult DAX-1 Orphan Nuclear Receptor DNA Mutational Analysis DNA-Binding Proteins / genetics* DNA-Binding Proteins / metabolism Female Genetic Diseases, X-Linked / genetics* Genetic Diseases, X-Linked / metabolism Humans Introns / genetics* Male Mutation* RNA Splicing / genetics RNA, Messenger / genetics RNA, Messenger / metabolism Receptors, Retinoic Acid / genetics* Receptors, Retinoic Acid / metabolism Repressor Proteins / genetics* Repressor Proteins / metabolism
Times Cited 5
WOS Category ENDOCRINOLOGY & METABOLISM
Resource
Human and Animal Cells COS-1 (RCB0143)