Home News About Us Contact Contributors Disclaimer Privacy Policy Help FAQ

Home
Search
Quick Search
Advanced
Fulltext
Browse
Collections
Persons
My eDoc
Session History
Login
Name:
Password:
Documentation
Help
Support Wiki
Direct access to
document ID:


          Institute: MPI für molekulare Genetik     Collection: Research Group Development and Disease     Display Documents



  history
ID: 25766.0, MPI für molekulare Genetik / Research Group Development and Disease
Association of the 867Asp variant of the human anion exchanger 3 gene with common subtypes of idiopathic generalized epilepsy
Authors:Sander, Thomas; Toliat, Mohammad Reza; Heils, Armin; Leschik, Gundula; Becker, Christian; Rüschendorf, Franz; Rohde, Klaus; Mundlos, Stefan; Nürnberg, Peter
Language:English
Date of Publication (YYYY-MM-DD):2002-10-01
Title of Journal:Epilepsy Research
Volume:51
Issue / Number:3
Start Page:249
End Page:255
Review Status:not specified
Audience:Experts Only
Abstract / Description:Genetic factors play a major role in the etiology of idiopathic generalized epilepsies (IGE). Our recent genome-wide search revealed suggestive evidence for a susceptibility locus for common IGE syndromes in the chromosomal region 2q36. The gene encoding the anion exchanger isoform 3 (AE3; gene symbol: SLC4A3) has been mapped to this candidate region. AE3 is prominently expressed in the brain and performs an electroneutral exchange of chloride and bicarbonate. To study the potential role of AE3 in the epileptogenesis of IGE, we performed a mutation analysis of the AE3 coding region, including the adjacent exon/intron boundaries, and the 5'-untranslated region in 16 IGE probands of families linked to chromosome 2q36 (cumulative two-point lod score: Z=5.32 at D2S371). Three exonic sequence variants were found: exon 17: 2600C/A, Ala867Asp; exon 21: 3391C/T, Leu1131Leu; exon 23: 3771G/A, 3'-UTR. Our subsequent population-based association study of the Ala867Asp substitution polymorphism revealed a significant increase of the 867Asp variant in 366 unrelated German IGE patients compared with 183 German control subjects (2=5.37, DF=1, P=0.021). Consistently, the transmission disequilibrium test (TDT) of 121 parent–child trios showed a significant preferential transmission of the 867Asp allele (McNemar 2=5.81, DF=1, P=0.016). Our results support the hypothesis that variation of the AE3 gene confers a common but small susceptibility effect to the etiology of a broad spectrum of IGE syndromes.
Free Keywords:Idiopathic generalized epilepsy; Mutation analysis; Anion exchanger AE3; Chromosome 2
External Publication Status:published
Document Type:Article
Communicated by:Stefan Mundlos
Affiliations:MPI für molekulare Genetik
External Affiliations:Department of Neurology, Epilepsy Genetics Group, University Clinic Charité, Humboldt University of Berlin, Augustenburger Platz 1, 13353, Berlin
Institute of Medical Genetics, University Clinic Charité, Humboldt University of Berlin, Augustenburger Platz 1, 13353, Berlin
Gene Mapping Center, Max-Delbrueck-Center for Molecular Medicine, Robert-Roessle-Str. 10, 13092, Berlin
Bioinformatics, Max-Delbrueck-Center for Molecular Medicine, Robert-Roessle-Str. 10, 13092, Berlin
Department of Human Genetics, Rheinische Friedrich-Wilhelms-University of Bonn, Wilhelmstr. 31, 53111, Bonn
Institute for Medical Biometry, Informatics and Epidemiology, University of Bonn, Sigmund-Freud-Str. 25, 53105, Bonn
The scope and number of records on eDoc is subject to the collection policies defined by each institute - see "info" button in the collection browse view.