Association analysis of chromosome 15 GABAA receptor subunit genes in autistic disorder

被引:119
作者
Menold, MM
Shao, YJ
Wolpert, CM
Donnelly, SL
Raiford, KL
Martin, ER
Ravan, SA
Abramson, RK
Wright, HH
Delong, GR
Cuccaro, L
Pericak-Vance, MA
Gilbert, JR
机构
[1] Duke Univ, Med Ctr, Ctr Human Genet, Dept Med, Durham, NC 27710 USA
[2] Univ S Carolina, WS Hall Psychiat Inst, Columbia, SC 29202 USA
[3] Duke Univ, Med Ctr, Dept Med, Durham, NC 27710 USA
[4] Duke Univ, Med Ctr, Dept Pediat, Durham, NC 27710 USA
基金
美国国家卫生研究院;
关键词
single nucleotide polymorphism; autistic disorder; gamma aminobutyric acids; oligonucleotide ligation assay; chromosome; 15q11-q13;
D O I
10.3109/01677060109167380
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Gamma-aminobutyric acid (GABA) is the major inhibitory neurotransmitter in the brain, acting via the GABA(A) receptors. The GABA(A) receptors are comprised of several different homologous subunits, forming a group of receptors that are both structurally and functionally diverse. Three of the GABA(A) receptor subunit genes (GABRB3. GABRA5 and GABRG3) form a cluster on chromosome 15q11-q13, in a region that has been genetically associated with autistic disorder (AutD). Based on these data. we examined 16 single nucleotide polymorphisms (SNPs) located within GABRB3, GABRA5 and GABRG3 for linkage disequilibrium (LD) in 226 AutD families (AutD patients and parents). Genotyping was performed using either OLA (oligonucleotide ligation assay), or SSCP (single strand conformation polymorphism) followed by DNA sequencing. We tested for LD using the Pedigree Disequilibrium Test (PDT). PDT results gave significant evidence that AutD is associated with two SNPs located within the GABRG3 gene (exon5_539T/C, p = 0.02 and intron5_687T/C, p = 0.03), suggesting that the GABRG3 gene or a gene nearby contributes to genetic risk in AutD.
引用
收藏
页码:245 / 259
页数:15
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