No evidence for association between a non-synonymous polymorphism in the gene encoding human metabotropic glutamate receptor 7 and schizophrenia

被引:17
作者
Bray, NJ
Williams, NM
Bowen, T
Cardno, AG
Gray, M
Jones, LA
Murphy, KC
Sanders, RD
Spurlock, G
O'Donovan, MC
Owen, MJ
机构
[1] Cardiff Univ, Div Psychol Med, Cardiff CF4 4XN, S Glam, Wales
[2] Cardiff Univ, Div Med Genet, Cardiff CF4 4XN, S Glam, Wales
基金
英国医学研究理事会;
关键词
schizophrenia; mGluR7; gene; polymorphism; association studies; chromosome; 3p25-22;
D O I
10.1097/00041444-200010020-00005
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The cDNA sequence of the gene encoding human metabotropic glutamate receptor type 7 (mGluR7) contains the single nucleotide polymorphism 1536A>T [GenBank sequence X94552 (Makoff et al., 1996)]. This sequence variation is predicted to result in an amino acid change (F433Y) in the gene product and thus has the potential to affect receptor function. Since disturbances in glutamate function have been implicated in the pathophysiology of schizophrenia, we have used a novel and robust polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) assay to genotype this polymorphism in a case-control sample comprising 181 schizophrenic patients and 182 group-matched unaffected individuals. No evidence was found for association between this polymorphism and schizophrenia. We have also localised mGluR7 to chromosome 3p25-22 using radiation hybrid (RH) mapping. Psychiatr Genet 10:83-86 (C) 2000 Lippincott Williams & Wilkins.
引用
收藏
页码:83 / 86
页数:4
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