Coon H, Hoff M, Holik J, Delisi L E, Crowe T, Freedman R, Shields G, Boccio A M, Lerman M, Gershon E S
Department of Psychiatry, University of Utah Medical Center, Salt Lake City 84132.
Am J Med Genet. 1993 May 1;48(1):36-9. doi: 10.1002/ajmg.1320480109.
Jones et al. Nature Genet 1:306-309, [1992] recently detected a C to T nucleotide transition (codon 713) in a highly conserved region of the beta-amyloid precursor gene in a single case of schizophrenia. Although the sequence variant may be a natural polymorphism, it is crucial to determine whether the mutation might be present in a small subset of schizophrenics. We isolated DNA from 86 unrelated chronic schizophrenics who had a first degree relative with chronic schizophrenia or chronic schizoaffective disorder. After PCR amplification of exon 17, we were unable to detect the presence of the codon 713 variant in these schizophrenic cases, as well as in 156 controls. Unless additional cases are found with the codon 713 mutation, it is unlikely that the sequence variant is pathogenic for schizophrenia.
琼斯等人。《自然遗传学》1:306 - 309,[1992]最近在一例精神分裂症患者的β - 淀粉样前体蛋白基因高度保守区域检测到一个从C到T的核苷酸转变(密码子713)。尽管该序列变异可能是一种自然多态性,但确定该突变是否可能存在于一小部分精神分裂症患者中至关重要。我们从86名无亲缘关系的慢性精神分裂症患者中分离出DNA,这些患者有一位患有慢性精神分裂症或慢性分裂情感性障碍的一级亲属。在对外显子17进行PCR扩增后,我们在这些精神分裂症病例以及156名对照中均未检测到密码子713变异的存在。除非发现更多携带密码子713突变的病例,否则该序列变异不太可能是精神分裂症的致病因素。