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1.
Hum Mol Genet ; 13(13): 1315-9, 2004 Jul 01.
Artigo em Inglês | MEDLINE | ID: mdl-15115768

RESUMO

A major challenge in understanding complex idiopathic generalized epilepsies has been the characterization of their underlying molecular genetic basis. Here, we report that genetic variation within the GABRD gene, which encodes the GABAA receptor delta subunit, affects GABA current amplitude consistent with a model of polygenic susceptibility to epilepsy in humans. We have found a GABRD Glu177Ala variant which is heterozygously associated with generalized epilepsy with febrile seizures plus. We also report an Arg220His allele in GABRD which is present in the general population. Compared with wild-type receptors, alpha1beta2Sdelta GABAA receptors containing delta Glu177Ala or Arg220His have decreased GABAA receptor current amplitudes. As GABAA receptors mediate neuronal inhibition, the reduced receptor current associated with both variants is likely to be associated with increased neuronal excitability. Since delta subunit-containing receptors localize to extra- or peri-synaptic membranes and are thought to be involved in tonic inhibition, our results suggest that alteration of this process may contribute to the common generalized epilepsies.


Assuntos
Substituição de Aminoácidos/genética , Epilepsia Generalizada/genética , Predisposição Genética para Doença , Herança Multifatorial , Mutação Puntual , Receptores de GABA-A/genética , Epilepsia Generalizada/fisiopatologia , Feminino , Heterozigoto , Homozigoto , Humanos , Masculino , Linhagem , Convulsões Febris/genética , Convulsões Febris/fisiopatologia , Membranas Sinápticas/patologia
2.
Am J Hum Genet ; 70(2): 530-6, 2002 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-11748509

RESUMO

Recent findings from studies of two families have shown that mutations in the GABA(A)-receptor gamma2 subunit are associated with generalized epilepsies and febrile seizures. Here we describe a family that has generalized epilepsy with febrile seizures plus (GEFS(+)), including an individual with severe myoclonic epilepsy of infancy, in whom a third GABA(A)-receptor gamma2-subunit mutation was found. This mutation lies in the intracellular loop between the third and fourth transmembrane domains of the GABA(A)-receptor gamma2 subunit and introduces a premature stop codon at Q351 in the mature protein. GABA sensitivity in Xenopus laevis oocytes expressing the mutant gamma2(Q351X) subunit is completely abolished, and fluorescent-microscopy studies have shown that receptors containing GFP-labeled gamma2(Q351X) protein are retained in the lumen of the endoplasmic reticulum. This finding reinforces the involvement of GABA(A) receptors in epilepsy.


Assuntos
Epilepsia Generalizada/genética , Receptores de GABA-A/química , Receptores de GABA-A/genética , Convulsões Febris/genética , Deleção de Sequência/genética , Animais , Sequência de Bases , Linhagem Celular , Códon de Terminação/genética , Eletrofisiologia , Retículo Endoplasmático/metabolismo , Epilepsias Mioclônicas/complicações , Epilepsias Mioclônicas/genética , Epilepsia Generalizada/complicações , Feminino , Humanos , Masculino , Modelos Moleculares , Oócitos/efeitos dos fármacos , Oócitos/metabolismo , Linhagem , Conformação Proteica , Subunidades Proteicas , Receptores de GABA-A/metabolismo , Convulsões Febris/complicações , Xenopus laevis , Ácido gama-Aminobutírico/farmacologia
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