Latham T, Grabowski G A, Theophilus B D, Smith F I
Department of Microbiology, Mount Sinai School of Medicine, New York, NY 10029.
Am J Hum Genet. 1990 Jul;47(1):79-86.
Gaucher disease is inherited in an autosomal recessive manner and is the most prevalent lysosomal storage disease. Gaucher disease has marked phenotypic variation and molecular heterogeneity, and seven point mutations in the acid beta-glucosidase (beta-Glc) gene have been identified. By means of sequence-specific oligonucleotides (SSO), mutation 6433C has been detected homozygously in neuronopathic type 2 (acute) and type 3 (subacute) patients, as well as in children with severe visceral involvement who are apparently free of neuronopathic disease. To investigate the molecular basis for this puzzling finding, amplified beta-Glc cDNAs from 6433C homozygous type 2 and type 3 Gaucher disease patients were cloned and sequenced. The Swedish type 3 Gaucher disease patient was truly homozygous for alleles only containing the 6433C mutation. In comparison, the type 2 patient contained a singly mutated 6433C allele and a "complex" allele with multiple discrete point mutations (6433C, 6468C, and 6482C). Each of the mutations in the complex allele also was present in the beta-Glc pseudogene. SSO hybridization of 6433C homozygotes revealed that both type 2 patients contained additional mutations in one allele, whereas the 6433C alone was detected in both type 3 and in young severe type 1 Gaucher disease patients. These results suggest that the presence of the complex allele influences the severity of neuronopathic disease in 6433C homozygotes and reveal the central role played by the pseudogene in the formation of mutant alleles of the beta-Glc gene. Analysis of additional cDNA clones also identified two new alleles in a type 3 patient, emphasizing the molecular heterogeneity of neuronopathic Gaucher disease.
戈谢病以常染色体隐性方式遗传,是最常见的溶酶体贮积病。戈谢病具有显著的表型变异和分子异质性,已在酸性β-葡萄糖苷酶(β-Glc)基因中鉴定出7个点突变。通过序列特异性寡核苷酸(SSO),在2型(急性)和3型(亚急性)神经病变型患者以及明显无神经病变的严重内脏受累儿童中均检测到纯合的6433C突变。为了探究这一令人困惑的发现的分子基础,对来自6433C纯合2型和3型戈谢病患者的扩增β-Glc cDNA进行了克隆和测序。瑞典3型戈谢病患者对于仅含有6433C突变的等位基因而言确实是纯合的。相比之下,2型患者含有一个单突变的6433C等位基因和一个带有多个离散点突变(6433C、6468C和6482C)的“复杂”等位基因。复杂等位基因中的每个突变也存在于β-Glc假基因中。6433C纯合子的SSO杂交显示,两名2型患者在一个等位基因中均含有额外的突变,而在3型和年轻的严重1型戈谢病患者中均仅检测到6433C。这些结果表明,复杂等位基因的存在会影响6433C纯合子中神经病变疾病的严重程度,并揭示了假基因在β-Glc基因突变等位基因形成中所起的核心作用。对其他cDNA克隆的分析还在一名3型患者中鉴定出两个新的等位基因,强调了神经病变型戈谢病的分子异质性。