Dazzo C, Tolan D R
Department of Biology, Boston University, MA 02215.
Am J Hum Genet. 1990 Jun;46(6):1194-9.
Hereditary fructose intolerance (HFI) is an inborn error of metabolism, inherited as an autosomal recessive disorder and caused by a decrease in the activity of fructose-1-phosphate aldolase (aldolase B) in affected individuals. Investigation of the molecular basis of HFI is reported here by the identification of two molecular lesions in the aldolase B gene of the HFI individual. Using polymerase chain reaction to specifically amplify exons at this locus and T7 polymerase for the sequence determination of these double-stranded fragments, we show the mutational heterogeneity of the proband. One allele, previously indicated by restriction analysis, was confirmed as A149P (Ala 149 to Pro in exon 5). The other allele was identified as a 4-bp deletion found in exon 4, a deletion which causes a frameshift at codon 118, resulting in a truncated protein of 132 amino acids. Segregation of these mutant alleles in the proband's family was shown by using allele-specific oligodeoxynucleotides to probe blots of amplified DNA. The techniques employed here represent a rapid and efficient method for detection of other mutations in families with this disease. In addition, the ability to detect mutant alleles by allele-specific hybridization offers a new method for definitive diagnosis, a method which avoids a fructose loading or liver-biopsy examination.
遗传性果糖不耐受症(HFI)是一种先天性代谢缺陷病,以常染色体隐性障碍的方式遗传,患病个体中果糖-1-磷酸醛缩酶(醛缩酶B)的活性降低。本文通过鉴定HFI个体醛缩酶B基因中的两个分子损伤,报道了对HFI分子基础的研究。利用聚合酶链反应特异性扩增该位点的外显子,并使用T7聚合酶对这些双链片段进行序列测定,我们展示了先证者的突变异质性。通过限制性分析先前已指出的一个等位基因,经确认是A149P(第5外显子中丙氨酸149突变为脯氨酸)。另一个等位基因被鉴定为在第4外显子中发现的4个碱基的缺失,该缺失导致密码子118处的移码,产生一个132个氨基酸的截短蛋白。通过使用等位基因特异性寡脱氧核苷酸探测扩增DNA的印迹,展示了先证者家族中这些突变等位基因的分离情况。这里采用的技术是检测患有这种疾病家族中其他突变的一种快速有效的方法。此外,通过等位基因特异性杂交检测突变等位基因的能力提供了一种明确诊断的新方法,这种方法避免了果糖负荷试验或肝活检检查。