A novel V59E missense mutation in the sodium iodide symporter gene in a family with iodide transport defect

Thyroid. 2000 Jun;10(6):471-4. doi: 10.1089/thy.2000.10.471.

Abstract

Iodide transport defect results from the malfunction of iodide transporter (sodium iodide symporter [NIS]), and is characterized by low uptake of iodide into thyroid cells. Genetic analysis revealed that a T354P missense mutation causes iodide transport defect in the homozygous state and is a frequent mutation in the Japanese population. We recently reported three siblings with iodide transport defect harboring the T354P mutation in the heterozygous state. Here we report a novel V59E missense mutation associated with these siblings. The mutant protein showed low iodide transport activity.

MeSH terms

  • Adult
  • Amino Acid Sequence
  • Biological Transport, Active
  • Carrier Proteins / genetics*
  • Cell Line
  • Child, Preschool
  • DNA / analysis
  • DNA / genetics
  • Humans
  • Iodides / metabolism*
  • Membrane Proteins / genetics*
  • Metabolism, Inborn Errors / genetics*
  • Metabolism, Inborn Errors / metabolism
  • Molecular Sequence Data
  • Mutation, Missense / genetics*
  • Pedigree
  • Reverse Transcriptase Polymerase Chain Reaction
  • Symporters*

Substances

  • Carrier Proteins
  • Iodides
  • Membrane Proteins
  • Symporters
  • sodium-iodide symporter
  • DNA