Bowen T, Guy C, Speight G, Jones L, Cardno A, Murphy K, McGuffin P, Owen M J, O'Donovan M C
Department of Psychological Medicine, University of Wales College of Medicine, Cardiff.
Am J Hum Genet. 1996 Oct;59(4):912-7.
Studies of the transmission of schizophrenia in families with affected members in several generations have suggested that an expanded trinucleotide repeat mechanism may contribute to the genetic inheritance of this disorder. Using repeat expansion detection (RED), we and others have previously found that the distribution of CAG/CTG repeat size is larger in patients with schizophrenia than in controls. In an attempt to identify the specific expanded CAG/CTG locus or loci associated with schizophrenia, we have now used an approach based on a CAG/CTG PCR screening set combined with RED data. This has allowed us to minimize genotyping while excluding 43 polymorphic autosomal loci and 7 X-chromosomal loci from the screening set as candidates for expansion in schizophrenia with a very high degree of confidence.
对几代人中均有患病成员的家族性精神分裂症传播的研究表明,三核苷酸重复序列扩展机制可能在这种疾病的遗传中起作用。通过重复序列扩展检测(RED),我们和其他人之前发现,精神分裂症患者中CAG/CTG重复序列大小的分布比对照组更大。为了确定与精神分裂症相关的特定扩展CAG/CTG位点,我们现在采用了一种基于CAG/CTG PCR筛选集并结合RED数据的方法。这使我们能够在将43个多态性常染色体位点和7个X染色体位点从筛选集中排除作为精神分裂症中扩展候选位点的同时,以非常高的置信度将基因分型降至最低。