Exome sequencing of a pedigree with Tourette syndrome or chronic tic disorder

Ann Neurol. 2011 May;69(5):901-4. doi: 10.1002/ana.22398.

Abstract

Ten members of a 3-generation pedigree with 7 showing Tourette syndrome/chronic tic phenotype (TS-CTD) were evaluated with whole exome sequencing. We identified 3 novel, nonsynonymous single nucleotide variants in the MRPL3, DNAJC13, and OFCC1 genes that segregated with chronic tic phenotype. These variants were not present in 100 control subjects or in dbSNP/1000 Genomes databases. A novel variant in the 5' untranslated region of the OFCC1 gene was found in 2 TS-CTD patients from a different pedigree. Further studies will clarify the importance of variants in MRPL3, DNAJC13, and OFCC1 genes in TS.

MeSH terms

  • Chronic Disease
  • DNA Mutational Analysis
  • Family Health
  • Female
  • Genetic Linkage
  • HSP40 Heat-Shock Proteins / genetics
  • Humans
  • Male
  • Mitochondrial Proteins / genetics
  • Pedigree*
  • Phenotype
  • Polymorphism, Single Nucleotide / genetics
  • Proteins / genetics
  • Sequence Alignment / methods
  • Tic Disorders / complications
  • Tic Disorders / genetics*
  • Tourette Syndrome / complications
  • Tourette Syndrome / genetics*

Substances

  • DNAJC3 protein, human
  • HSP40 Heat-Shock Proteins
  • Mitochondrial Proteins
  • OFCC1 protein, human
  • Proteins