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J Clin Endocrinol Metab. 2010 Aug;95(8):4066-71. doi: 10.1210/jc.2009-2611. Epub 2010 May 25.

Selenoprotein-related disease in a young girl caused by nonsense mutations in the SBP2 gene.

Author information

1
Department of Pediatrics, Faculty of Medicine, University Hospital of Brasília, Faculty of Health Sciences, University of Brasília, SGAN Quadra 605, Asa Norte, Prédio Novo de Ambulatórios, 70840-901, Brasília-DF, Brazil. monalisa@unb.br

Abstract

CONTEXT:

Selenoproteins are essential for life, and their biosynthesis requires the incorporation of the rare amino acid selenocysteine (Sec) in a process mediated by the Sec insertion sequence-binding protein 2 (SBP2). Although SBP2 is considered a rate-limiting factor mediating Sec incorporation, there has been little evidence so far linking SBP2 dysfunction to widespread selenoprotein-related disease.

OBJECTIVE:

The objective of the study was to report the discovery of novel truncation mutations in the SBP2 gene (R120X/R770X) in a female adolescent and the clinical consequences of the combined deficiency of selenoproteins.

SUBJECTS AND METHODS:

A 12-yr-old girl who presented with a syndrome of abnormal thyroid hormone metabolism, delayed bone maturation, congenital myopathy, and impaired mental and motor coordination development and her family were studied. The coding region of the SBP2 gene was analyzed by sequencing, and gel shift assays were performed to address the in vitro binding properties of the mutant SBP2 protein.

RESULTS:

Serum levels of selenium and glutathione peroxidase in the proband were reduced, and selenoprotein P levels were undetectable. DNA sequencing of the SBP2 gene revealed a compound heterozygous mutation (R120X/R770X). The R120X mutation disrupted all functional motifs and the R770X inhibited the binding of SBP2 to Sec insertion sequence elements. Interestingly, selenium supplementation normalized serum selenium and glutathione peroxidase but not selenoprotein P levels and did not restore thyroid hormone metabolism dysfunction.

CONCLUSIONS:

This distinctive phenotype can only be explained by the combined deficiency of functionally important selenoproteins and pinpoints the clinical relevance of selenoproteins and selenium economy in human development.

Comment in

PMID:
20501692
DOI:
10.1210/jc.2009-2611
[Indexed for MEDLINE]

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