A missense mutation of the Na+ channel αII subunit gene Nav1.2 in a patient with febrile and afebrile seizures causes channel dysfunction

Generalized epilepsy with febrile seizures plus (GEFS+), a clinical subset of febrile seizures (FS), is characterized by frequent episodes beyond 6 years of age (FS+) and various types of subsequent epilepsy. Mutations in β1 and α I -subunit genes of voltage-gated Na + channels have been associated...

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Published in:Proceedings of the National Academy of Sciences - PNAS 2001-05, Vol.98 (11), p.6384-6389
Main Authors: Sugawara, Takashi, Tsurubuchi, Yuji, Agarwala, Kishan Lal, Ito, Masatoshi, Fukuma, Goryu, Mazaki-Miyazaki, Emi, Nagafuji, Hiroshi, Noda, Masaharu, Imoto, Keiji, Wada, Kazumaru, Mitsudome, Akihisa, Kaneko, Sunao, Montal, Mauricio, Nagata, Keiichi, Hirose, Shinichi, Yamakawa, Kazuhiro
Format: Article
Language:English
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Biological Sciences
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Summary:Generalized epilepsy with febrile seizures plus (GEFS+), a clinical subset of febrile seizures (FS), is characterized by frequent episodes beyond 6 years of age (FS+) and various types of subsequent epilepsy. Mutations in β1 and α I -subunit genes of voltage-gated Na + channels have been associated with GEFS+1 and 2, respectively. Here, we report a mutation resulting in an amino acid exchange (R187W) in the gene encoding the α-subunit of neuronal voltage-gated Na + channel type II ( Na v 1.2 ) in a patient with FS associated with afebrile seizures. The mutation R187W occurring on Arg 187 , a highly conserved residue among voltage-gated Na + channels, was not found in 224 alleles of unaffected individuals. Whole-cell patch clamp recordings on human embryonic kidney (HEK) cells expressing a rat wild-type (rNa v 1.2) and the corresponding mutant channels showed that the mutant channel inactivated more slowly than wild-type whereas the Na + channel conductance was not affected. Prolonged residence in the open state of the R187W mutant channel may augment Na + influx and thereby underlie the neuronal hyperexcitability that induces seizure activity. Even though a small pedigree could not show clear cosegregation with the disease phenotype, these findings strongly suggest the involvement of Na v 1.2 in a human disease and propose the R187W mutation as the genetic defect responsible for febrile seizures associated with afebrile seizures. febrile seizures epilepsy channelopathy
ISSN:0027-8424
1091-6490
DOI:10.1073/pnas.111065098