Developmental impact of a familial GABAA receptor epilepsy mutation

Ann Neurol. 2008 Sep;64(3):284-93. doi: 10.1002/ana.21440.

Abstract

Objective: A major goal of epilepsy research is to understand the molecular and functional basis of seizure genesis. A human GABA(A) gamma2 gene mutation (R43Q) is associated with generalized epilepsy. Introduction of this mutation into a mouse by gene targeting recapitulates the human phenotype demonstrating a strong genotype to phenotype link. GABA(A) receptors play a role in the moment-to-moment control of brain function and also on the long-term wiring of the brain by directing neuronal development. Our objective was to determine whether developmental expression of the mutation alters seizure susceptibility later in life.

Methods: A tetracycline-based conditional model for activation of a hypomorphic Q43 disease allele was created and validated. Seizure susceptibility was assessed using the subcutaneous pentylenetetrazole model.

Results: Seizure susceptibility was significantly reduced in mice where the Q43 allele was suppressed during development.

Interpretation: These results demonstrate that a human epilepsy-causing mutation impacts network stability during a critical developmental period. These data suggest that identification of presymptomatic children may provide a window for therapeutic intervention before overt symptoms are observed, potentially altering the course of epileptogenesis.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Brain / metabolism*
  • Brain / physiopathology
  • Brain Chemistry / genetics
  • Convulsants
  • Disease Models, Animal
  • Epilepsy / genetics*
  • Epilepsy / metabolism*
  • Epilepsy / physiopathology
  • Genetic Predisposition to Disease / genetics*
  • Humans
  • Mice
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • Mutation / genetics*
  • Nerve Net / physiopathology
  • Neural Inhibition / genetics
  • Pentylenetetrazole
  • Receptors, GABA-A / genetics*
  • Tetracycline / pharmacology
  • gamma-Aminobutyric Acid / metabolism

Substances

  • Convulsants
  • GABRG2 protein, human
  • Gabrg2 protein, mouse
  • Receptors, GABA-A
  • gamma-Aminobutyric Acid
  • Tetracycline
  • Pentylenetetrazole