An allele of COL9A2 associated with intervertebral disc disease

Science. 1999 Jul 16;285(5426):409-12. doi: 10.1126/science.285.5426.409.

Abstract

Intervertebral disc disease is one of the most common musculoskeletal disorders. A number of environmental and anthropometric risk factors may contribute to it, and recent reports have suggested the importance of genetic factors as well. The COL9A2 gene, which codes for one of the polypeptide chains of collagen IX that is expressed in the intervertebral disc, was screened for sequence variations in individuals with intervertebral disc disease. The analysis identified a putative disease-causing sequence variation that converted a codon for glutamine to one for tryptophan in six out of the 157 individuals but in none of 174 controls. The tryptophan allele cosegregated with the disease phenotype in the four families studied, giving a lod score (logarithm of odds ratio) for linkage of 4.5, and subsequent linkage disequilibrium analysis conditional on linkage gave an additional lod score of 7.1.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adult
  • Aged
  • Alleles
  • Amino Acid Substitution
  • Case-Control Studies
  • Codon
  • Collagen / chemistry
  • Collagen / genetics*
  • Collagen Type IX*
  • Female
  • Genetic Linkage
  • Genetic Predisposition to Disease*
  • Humans
  • Intervertebral Disc Displacement / genetics*
  • Linkage Disequilibrium
  • Male
  • Middle Aged
  • Mutation
  • Penetrance
  • Polymorphism, Genetic
  • Sciatica / genetics*
  • Tryptophan / genetics

Substances

  • COL9A2 protein, human
  • Codon
  • Collagen Type IX
  • Tryptophan
  • Collagen