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Candidate gene analysis of the human metabotropic glutamate receptor type 4 ( GRM4 ) in patients with juvenile myoclonic epilepsy
Author(s) -
Izzi Claudia,
Barbon Alessandro,
Toliat Mohammad Reza,
Heils Armin,
Becker Christian,
Nürnberg Peter,
Sander Thomas,
Barlati Sergio
Publication year - 2003
Publication title -
american journal of medical genetics part b: neuropsychiatric genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.393
H-Index - 126
eISSN - 1552-485X
pISSN - 1552-4841
DOI - 10.1002/ajmg.b.20024
Subject(s) - genetics , juvenile myoclonic epilepsy , idiopathic generalized epilepsy , biology , single nucleotide polymorphism , exon , locus (genetics) , candidate gene , population , linkage disequilibrium , genotype , gene , epilepsy , medicine , environmental health , neuroscience
Hereditary factors play a major role in the genetically complex etiology of juvenile myoclonic epilepsy (JME). Linkage studies in families of JME probands suggest a susceptibility locus ( EJM1 ) for idiopathic generalized epilepsy (IGE) in the chromosomal region 6p21.3 near the HLA region. The gene encoding the metabotropic glutamate receptor type 4 ( GRM4 ) has been localized within the EJM1 ‐region and represents a high‐ranking candidate gene. Therefore, we have sequenced the coding regions and regulatory GRM4 sequences in 20 IGE probands who were derived from families of JME probands providing positive linkage evidence to the HLA‐DQ locus. Our mutation analysis detected three synonymous exonic single nucleotide polymorphisms (SNP; exon‐7: c.1455T > C, exon‐8: c.2002A > G, exon‐10: c.2733C > T), one SNP in the 3′‐untranslated region (c.2890A > G), and two intronic SNPs (intron‐3: IVS3 + 2732A > G, intron‐7: IVS7 + 39C > T). None of the identified SNPs was likely to affect receptor function or gene expression. The population‐based association study did not show significant differences in the allele and genotype frequencies of the common c.1455T > C SNP between 144 German JME probands and 144 healthy population controls ( P > 0.84). Likewise, the family‐based transmission disequilibrium test did not indicate a preferential transmission of exon‐7 SNP alleles in 31 informative parent–child transmissions ( P = 0.86). Our results provide no evidence that genetic variation of the GRM4 gene confers susceptibility to JME‐related IGE syndromes. © 2003 Wiley‐Liss, Inc.