A GABRB3 promoter haplotype associated with childhood absence epilepsy impairs transcriptional activity

Hum Mol Genet. 2006 Aug 15;15(16):2533-41. doi: 10.1093/hmg/ddl174. Epub 2006 Jul 11.

Abstract

Childhood absence epilepsy (CAE) is considered to exhibit a complex non-Mendelian pattern of inheritance. So far, only few CAE susceptibility genes have been identified. In a previous study of our group, an association between the GABA(A) receptor beta3 subunit (GABRB3) gene and CAE was shown. To further investigate this association, we screened 45 CAE patients of the first study for mutations in the 10 exons, the exon-intron boundaries and the regulatory sequences of GABRB3. Although we found no functionally relevant mutation, we did identify 13 single nucleotide polymorphisms (SNPs) in the GABRB3 gene region from the exon 1a promoter to the beginning of intron 3. Using these SNPs we defined four haplotypes for the respective GABRB3 gene region. A transmission disequilibrium test in the same 45 CAE patients and their parents indicated a significant association of this region and CAE (P=0.007075). Reporter gene assays in NT2 cells using exon 1a promoter constructs indicated that the disease-associated haplotype 2 promoter causes a significantly lower transcriptional activity than the haplotype 1 promoter that is over-represented in the controls. In silico analysis suggested that an exchange from T (haplotype 1) to C (haplotype 2) within this promoter impairs binding of the neuron-specific transcriptional activator N-Oct-3. Electrophoretic mobility shift assays demonstrated that the respective polymorphism reduces the nuclear protein binding affinity, thus explaining the results of the reporter gene assays. Reduced expression of the GABRB3 gene could therefore be one potential cause for the development of CAE, pathogenetically relevant in our patient group.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Carrier Proteins
  • Cells, Cultured
  • Child
  • Computational Biology / methods
  • Electrophoretic Mobility Shift Assay
  • Epilepsy, Absence / genetics*
  • Gene Frequency
  • Genetic Linkage
  • Genetic Testing
  • Haplotypes*
  • Humans
  • Mutation
  • Nuclear Proteins / metabolism
  • Polymorphism, Single Nucleotide
  • Promoter Regions, Genetic
  • Receptors, GABA-A / genetics*
  • Receptors, GABA-A / physiology
  • Transcriptional Activation / genetics*

Substances

  • Carrier Proteins
  • GABRB3 protein, human
  • Nuclear Proteins
  • Receptors, GABA-A