Whole-exome sequencing, without prior linkage, identifies a mutation in LAMB3 as a cause of dominant hypoplastic amelogenesis imperfecta

Eur J Hum Genet. 2014 Jan;22(1):132-5. doi: 10.1038/ejhg.2013.76. Epub 2013 May 1.

Abstract

The conventional approach to identifying the defective gene in a family with an inherited disease is to find the disease locus through family studies. However, the rapid development and decreasing cost of next generation sequencing facilitates a more direct approach. Here, we report the identification of a frameshift mutation in LAMB3 as a cause of dominant hypoplastic amelogenesis imperfecta (AI). Whole-exome sequencing of three affected family members and subsequent filtering of shared variants, without prior genetic linkage, sufficed to identify the pathogenic variant. Simultaneous analysis of multiple family members confirms segregation, enhancing the power to filter the genetic variation found and leading to rapid identification of the pathogenic variant. LAMB3 encodes a subunit of Laminin-5, one of a family of basement membrane proteins with essential functions in cell growth, movement and adhesion. Homozygous LAMB3 mutations cause junctional epidermolysis bullosa (JEB) and enamel defects are seen in JEB cases. However, to our knowledge, this is the first report of dominant AI due to a LAMB3 mutation in the absence of JEB.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amelogenesis Imperfecta / etiology
  • Amelogenesis Imperfecta / genetics*
  • Amelogenesis Imperfecta / pathology
  • Cell Adhesion Molecules / genetics*
  • Cell Adhesion Molecules / metabolism
  • Epidermolysis Bullosa, Junctional / genetics
  • Epidermolysis Bullosa, Junctional / pathology
  • Exome
  • Female
  • Frameshift Mutation*
  • Genetic Linkage
  • High-Throughput Nucleotide Sequencing
  • Humans
  • Kalinin
  • Male
  • Pedigree

Substances

  • Cell Adhesion Molecules

Supplementary concepts

  • Amelogenesis Imperfecta, Type IB