A missense mutation of HOXA13 underlies hand-foot-genital syndrome in a Chinese family

J Genet. 2017 Sep;96(4):647-652. doi: 10.1007/s12041-017-0810-y.

Abstract

Hand-foot-genital syndrome (HFGS) is a rare autosomal dominant inherited syndrome characterized by limb malformations and urogenital defects. HFGS is caused by mutations in the HOXA13 gene. The aim of this study was to identify causative mutations in individuals and to explore the molecular pathogenesis in a Chinese family with HFGS. We performed Sanger sequencing and identified a recurrent missense mutation in the homeodomain (c.1123G>T, p.V375F) of HOXA13, molecular modelling predicted the mutation would affect DNA binding, and a luciferase reporter assay indicated that it impaired the ability of HOXA13 to activate transcription of the human EPHA7 promoter. This is the first report of the molecular basis for HFGS caused by missense mutations of HOXA13.

MeSH terms

  • Abnormalities, Multiple / diagnosis*
  • Abnormalities, Multiple / genetics*
  • China
  • DNA Mutational Analysis
  • Family
  • Female
  • Foot Deformities, Congenital / diagnosis*
  • Foot Deformities, Congenital / genetics*
  • Genetic Association Studies
  • Genotype
  • Hand Deformities, Congenital / diagnosis*
  • Hand Deformities, Congenital / genetics*
  • Homeodomain Proteins / chemistry
  • Homeodomain Proteins / genetics*
  • Humans
  • Male
  • Models, Molecular
  • Mutation, Missense*
  • Pedigree
  • Phenotype
  • Promoter Regions, Genetic
  • Protein Conformation
  • Urogenital Abnormalities / diagnosis*
  • Urogenital Abnormalities / genetics*

Substances

  • Homeodomain Proteins
  • homeobox protein HOXA13

Supplementary concepts

  • Hand foot uterus syndrome