A locus on mouse chromosome 2 is involved in susceptibility to congenital hypothyroidism and contains an essential gene expressed in thyroid

Endocrinology. 2010 Apr;151(4):1948-58. doi: 10.1210/en.2009-1240. Epub 2010 Feb 16.

Abstract

We report here the mapping of a chromosomal region responsible for strain-specific development of congenital hypothyroidism in mice heterozygous for null mutations in genes encoding Nkx2-1/Titf1 and Pax8. The two strains showing a differential predisposition to congenital hypothyroidism contain several single-nucleotide polymorphisms in this locus, one of which leads to a nonsynonymous amino acid change in a highly conserved region of Dnajc17, a member of the type III heat-shock protein-40 (Hsp40) family. We demonstrate that Dnajc17 is highly expressed in the thyroid bud and had an essential function in development, suggesting an important role of this protein in organogenesis and/or function of the thyroid gland.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blotting, Western
  • Cells, Cultured
  • Chromosome Mapping
  • Chromosomes, Mammalian / genetics
  • Congenital Hypothyroidism / genetics*
  • Congenital Hypothyroidism / metabolism
  • Genetic Association Studies
  • Genetic Predisposition to Disease / genetics*
  • HSP40 Heat-Shock Proteins / genetics*
  • HSP40 Heat-Shock Proteins / metabolism
  • Immunohistochemistry
  • Mice
  • Reverse Transcriptase Polymerase Chain Reaction
  • Thyroid Gland / abnormalities*
  • Thyroid Gland / metabolism
  • Thyrotropin / blood

Substances

  • HSP40 Heat-Shock Proteins
  • Thyrotropin