Kugler W, Lakomek M
Universitäts-Kinderklinik, Göttingen, Germany.
Baillieres Best Pract Res Clin Haematol. 2000 Mar;13(1):89-101. doi: 10.1053/beha.1999.0059.
Most of the metabolic needs of erythrocytes are covered by glycolysis, the oxidative pentose phosphate pathway and the glutathione cycle. Hereditary enzyme deficiencies of all these pathways have been identified, among which glucose-6-phosphate isomerase (GPI) deficiency is the second most frequent erythroenzymopathy in glycolysis, being associated with non-spherocytic haemolytic anaemia of variable severity. This autosomal recessive genetic disorder may be associated in some cases with neurological impairment. GPI is a dimeric enzyme that catalyses the reversible interconversion of fructose-6-phosphate and glucose-6-phosphate. Virtually all the mutant gene products reported are characterized by marked instability and normal substrate affinities, but altered catalytic activity and electrophoretic migration rates. At the nucleotide level, 29 mutations have been reported. This chapter reviews (a) the clinical pattern of the condition; (b) biochemical and molecular studies; (c) structure-function relationships; (d) the molecular basis of neurological dysfunctions sometimes associated with GPI deficiency; and (e) the correlation between the severity of the anaemia and the molecular defect.
红细胞的大多数代谢需求由糖酵解、氧化戊糖磷酸途径和谷胱甘肽循环满足。所有这些途径的遗传性酶缺乏症均已被发现,其中葡萄糖-6-磷酸异构酶(GPI)缺乏症是糖酵解中第二常见的红细胞酶病,与严重程度各异的非球形细胞溶血性贫血相关。这种常染色体隐性遗传病在某些情况下可能与神经功能障碍有关。GPI是一种二聚体酶,催化果糖-6-磷酸和葡萄糖-6-磷酸的可逆相互转化。几乎所有报道的突变基因产物都具有明显的不稳定性和正常的底物亲和力,但催化活性和电泳迁移率发生了改变。在核苷酸水平上,已报道了29种突变。本章综述了(a)该病的临床模式;(b)生化和分子研究;(c)结构-功能关系;(d)有时与GPI缺乏症相关的神经功能障碍的分子基础;以及(e)贫血严重程度与分子缺陷之间的相关性。