Congenital hypothyroidism due to mutations in the sodium/iodide symporter. Identification of a nonsense mutation producing a downstream cryptic 3' splice site

Joachim Pohlenz, Ira M. Rosenthal, Roy E Weiss, Sissy M. Jhiang, Charles Burant, Samuel Refetoff

Research output: Contribution to journalArticle

91 Citations (Scopus)

Abstract

A 12-yr-old hypothyroid girl was diagnosed at birth as athyreotic because her thyroid gland could not be visualized by isotope scanning. Goiter development due to incomplete thyrotropin suppression, a thyroidal radioiodide uptake of < 1%, and a low saliva to plasma ratio of 2.5 suggested iodide (I-) transport defect. mRNA isolated from her thyroid gland and injected into Xenopus oocytes failed to increase I- transport. Sequencing of the entire Na+/I- symporter (NIS) cDNA revealed a C to G transversion of nucleotide (nt) 1146 in exon 6, resulting in a Gin 267 (CAG) to Glu (GAG) substitution. This missense mutation produces an NIS with undetectable I- transport activity when expressed in COS-7 cells. Although only this missense mutation was identified in thyroid and lymphocyte cDNA, genotyping revealed that the proposita and her unaffected brother and father were heterozygous for this mutation. However, amplification of cDNA with a primer specific for the wild-type nt 1146 yielded a sequence lacking 67 nt. Genomic DNA showed a C to G transversion of nt 1940, producing a stop codon as well as a new downstream cryptic 3' splice acceptor site in exon 13, responsible for the 67 nt deletion, frameshift, and premature stop predicting an NIS lacking 129 carboxy-terminal amino acids. This mutation was inherited from the mother and present in the unaffected sister. Thus, although the proposita is a compound heterozygote, because of the very low expression (< 2.5%) of one mutant allele, she is functionally hemizygous for an NIS without detectable bioactivity.

Original languageEnglish (US)
Pages (from-to)1028-1035
Number of pages8
JournalJournal of Clinical Investigation
Volume101
Issue number5
StatePublished - Mar 1 1998
Externally publishedYes

Fingerprint

Congenital Hypothyroidism
RNA Splice Sites
Nonsense Codon
Symporters
Nucleotides
Mutation
Thyroid Gland
Complementary DNA
Missense Mutation
Siblings
Exons
Terminator Codon
COS Cells
Goiter
Iodides
Thyrotropin
Heterozygote
Xenopus
Saliva
Fathers

Keywords

  • Allele-specific amplification
  • Frameshift
  • Genetics
  • Iodide transport
  • Thyroid

ASJC Scopus subject areas

  • Medicine(all)

Cite this

Congenital hypothyroidism due to mutations in the sodium/iodide symporter. Identification of a nonsense mutation producing a downstream cryptic 3' splice site. / Pohlenz, Joachim; Rosenthal, Ira M.; Weiss, Roy E; Jhiang, Sissy M.; Burant, Charles; Refetoff, Samuel.

In: Journal of Clinical Investigation, Vol. 101, No. 5, 01.03.1998, p. 1028-1035.

Research output: Contribution to journalArticle

Pohlenz, Joachim ; Rosenthal, Ira M. ; Weiss, Roy E ; Jhiang, Sissy M. ; Burant, Charles ; Refetoff, Samuel. / Congenital hypothyroidism due to mutations in the sodium/iodide symporter. Identification of a nonsense mutation producing a downstream cryptic 3' splice site. In: Journal of Clinical Investigation. 1998 ; Vol. 101, No. 5. pp. 1028-1035.
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