Congenital hyperthyroidism caused by a solitary toxic adenoma harboring a novel somatic mutation (serine281-->isoleucine) in the extracellular domain of the thyrotropin receptor.

Détails

ID Serval
serval:BIB_323063773B5C
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Titre
Congenital hyperthyroidism caused by a solitary toxic adenoma harboring a novel somatic mutation (serine281-->isoleucine) in the extracellular domain of the thyrotropin receptor.
Périodique
The Journal of clinical investigation
Auteur⸱e⸱s
Kopp P., Muirhead S., Jourdain N., Gu W.X., Jameson J.L., Rodd C.
ISSN
0021-9738 (Print)
ISSN-L
0021-9738
Statut éditorial
Publié
Date de publication
15/09/1997
Peer-reviewed
Oui
Volume
100
Numéro
6
Pages
1634-1639
Langue
anglais
Notes
Publication types: Case Reports ; Journal Article ; Research Support, Non-U.S. Gov't ; Research Support, U.S. Gov't, P.H.S.
Publication Status: ppublish
Résumé
Activating somatic mutations in the thyrotropin (TSH) receptor have been identified as a cause of hyperfunctioning thyroid adenomas, and germline mutations have been found in familial nonautoimmune hyperthyroidism and sporadic congenital hyperthyroidism. All mutations reported to date have been located in the transmembrane domain. We now report an example of an activating mutation in the extracellular, TSH-binding domain, found in a male infant with congenital hyperthyroidism due to a toxic adenoma. The pregnancy was remarkable for fetal tachycardia. Scintigraphic studies demonstrated a large nodule in the right lobe, and a hemithyroidectomy was performed at the age of 2 yr. Direct sequencing of the TSH receptor gene revealed a mutation in one allele resulting in a substitution of serine281 by isoleucine (Ser281--> Ile) in the extracellular domain. The mutation was restricted to the adenomatous tissue. Expression of the Ser281--> Ile mutation in vitro revealed an increase in basal cAMP levels. Affinity for TSH was increased by the mutation. These findings demonstrate that activating mutations can also occur in the extracellular domain of the TSH receptor, and support a model in which the extracellular domain serves to restrain receptor function in the absence of TSH or antibody-induced conformational changes.
Mots-clé
Adenoma/diagnostic imaging, Adenoma/genetics, Adenoma/parasitology, Cells, Cultured, Cyclic AMP/metabolism, Humans, Hyperthyroidism/genetics, Infant, Newborn, Isoleucine/genetics, Male, Mutation, Radionuclide Imaging, Receptors, Thyrotropin/genetics, Serine/genetics, Technetium Compounds, Thyroid Neoplasms/diagnostic imaging, Thyroid Neoplasms/genetics, Thyroid Neoplasms/pathology, Thyrotropin/pharmacology, Transfection, Ultrasonography
Pubmed
Web of science
Open Access
Oui
Création de la notice
30/12/2020 16:36
Dernière modification de la notice
31/12/2020 7:26
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