Sherman J B, Raben N, Nicastri C, Argov Z, Nakajima H, Adams E M, Eng C M, Cowan T M, Plotz P H
Arthritis and Rheumatism Branch, National Institute of Arthritis, Musculoskeletal, and Skin Diseases, National Institutes of Health, Bethesda, MD 20892.
Am J Hum Genet. 1994 Aug;55(2):305-13.
Phosphofructokinase (PFK) catalyzes the rate-limiting step of glycolysis. Deficiency of the muscle enzyme is manifested by exercise intolerance and a compensated hemolytic anemia. Case reports of this autosomal recessive disease suggest a predominance in Ashkenazi Jews in the United States. We have explored the genetic basis for this illness in nine affected families and surveyed the normal Ashkenazi population for the mutations we have found. Genomic DNA was amplified using PCR, and denaturing gradient-gel electrophoresis was used to localize exons with possible mutations. The polymorphic exons were sequenced or digested with restriction enzymes. A previously described splicing mutation, delta 5, accounted for 11 (61%) of 18 abnormal alleles in the nine families. A single base deletion leading to a frameshift mutation in exon 22 (delta C-22) was found in six of seven alleles. A third mutation, resulting in a nonconservative amino acid substitution in exon 4, accounted for the remaining allele. Thus, three mutations could account for all illness in this group, and two mutations could account for 17 of 18 alleles. In screening 250 normal Ashkenazi individuals for all three mutations, we found only one delta 5 allele. Clinical data revealed no correlation between the particular mutations and symptoms, but male patients were more symptomatic than females, and only males had frank hemolysis and hyperuricemia. Because PFK deficiency in Ashkenazi Jews is caused by a limited number of mutations, screening genomic DNA from peripheral blood for the described mutations in this population should enable rapid diagnosis without muscle biopsy.
磷酸果糖激酶(PFK)催化糖酵解的限速步骤。肌肉酶缺乏表现为运动不耐受和代偿性溶血性贫血。这种常染色体隐性疾病的病例报告表明在美国德系犹太人中更为常见。我们研究了九个患病家庭中这种疾病的遗传基础,并在正常德系犹太人群体中调查我们发现的突变。使用聚合酶链反应(PCR)扩增基因组DNA,并使用变性梯度凝胶电泳定位可能存在突变的外显子。对多态性外显子进行测序或用限制性酶消化。一个先前描述的剪接突变delta 5,在九个家庭的18个异常等位基因中占11个(61%)。在七个等位基因中的六个中发现了一个导致外显子22移码突变的单碱基缺失(delta C-22)。第三个突变导致外显子4中的一个非保守氨基酸替代,占其余的等位基因。因此,三个突变可以解释该组中的所有疾病,两个突变可以解释18个等位基因中的17个。在对250名正常德系犹太人个体进行所有三种突变的筛查中,我们仅发现一个delta 5等位基因。临床数据显示特定突变与症状之间无相关性,但男性患者比女性症状更明显,且只有男性有明显的溶血和高尿酸血症。由于德系犹太人中的PFK缺乏是由有限数量的突变引起的,因此在该人群中筛查外周血基因组DNA中的所述突变应能在无需肌肉活检的情况下实现快速诊断。