Clinical and molecular characterization of a novel selenocysteine insertion sequence-binding protein 2 (SBP2) gene mutation (R128X)

Caterina Di Cosmo, Neil McLellan, Xiao Hui Liao, Kum Kum Khanna, Roy E. Weiss, Laura Papp, Samuel Refetoff

Research output: Contribution to journalArticle

68 Scopus citations

Abstract

Context: Although acquired abnormalities of thyroid hormone metabolism arecommon,inherited defects in humans involving the synthesis of selenoproteins, including iodothyronine deiodinases, have been described in only one recent publication. Objective: We report the study of a novel selenocysteine insertion sequence-binding protein 2 (SBP2) gene mutation (R128X) and its clinical and molecular characterization. Subjects and Methods:Afamily of African origin was studied. The proband presented with growth retardation,lowserumselenium level,andthyroid test abnormalities consisting of highserumtotal and free T 4 concentrations associated with low T3, high rT 3, and normal TSH. The entire coding region of the SBP2 gene was sequenced and minigenes constructed to explain the nature of the defect. Results: The proband was homozygous for a nonsense gene mutation that produces an early stop codon (R128X). Both parents and a sister were heterozygous but showed no growth or thyroid test abnormalities. Despite the severity of the defect, the patient had a relatively mild phenotype, similar to that associated with partial SBP2 deficiency. In vitro analysis showed that the mutant minigene synthesized SBP2 from at least three downstream ATGs capable of generating molecules containing the essential functional domains. Treatment with L-T 3 accelerated the growth velocity and advanced the bone age. Conclusions: We identified a novel SBP2 gene mutation producing an early arrest in the synthesis of a full-length molecule. The demonstration that SBP2 isoforms containing all functional domains could be synthesized from three downstream ATGs explains the relatively mild phenotype caused by this defect.

Original languageEnglish (US)
Pages (from-to)4003-4009
Number of pages7
JournalJournal of Clinical Endocrinology and Metabolism
Volume94
Issue number10
DOIs
StatePublished - 2009

ASJC Scopus subject areas

  • Endocrinology, Diabetes and Metabolism
  • Biochemistry
  • Endocrinology
  • Clinical Biochemistry
  • Biochemistry, medical

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