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Research Article Free access | 10.1172/JCI118540

A circulating, biologically inactive thyrotropin caused by a mutation in the beta subunit gene.

G Medeiros-Neto, D T Herodotou, S Rajan, S Kommareddi, L de Lacerda, R Sandrini, M C Boguszewski, A N Hollenberg, S Radovick, and F E Wondisford

Thyroid Unit, Beth Israel Hospital, Boston, Massachusetts 02215, USA.

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Thyroid Unit, Beth Israel Hospital, Boston, Massachusetts 02215, USA.

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Thyroid Unit, Beth Israel Hospital, Boston, Massachusetts 02215, USA.

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Published March 1, 1996 - More info

Published in Volume 97, Issue 5 on March 1, 1996
J Clin Invest. 1996;97(5):1250–1256. https://doi.org/10.1172/JCI118540.
© 1996 The American Society for Clinical Investigation
Published March 1, 1996 - Version history
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Abstract

Mutation of a critical carboxy-terminal cysteine residue (C105V) in the thyrotropin-beta (TSH-beta) subunit gene was found in two related families with central hypothyroidism. Affected patients had low thyroid hormone levels and radioactive iodine uptake in the thyroid gland associated with measurable serum TSH. Thyrotropin-releasing hormone-stimulated TSH secretion did not increase thyroid hormone production in these patients as compared to their unaffected siblings, suggesting that the mutant TSH was biologically inactive in vivo. Recombinant TSH harboring this mutation was confirmed to be biologically inactive in an in vitro bioassay. Based on crystallographic structure of chorionic gonadotropin, a disulfide bond between C19 and C105 in the TSH-beta subunit is predicted to form the "buckle" of a "seat belt" that surrounds the common alpha subunit and maintains the conformation and bioactivity of the hormone. This natural mutation of the TSH-beta subunit confirms the importance of the seat belt in the family of pituitary and placental glycoprotein hormones.

Version history
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