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一例卟啉症患者中的尿卟啉原脱羧酶结构突变体(甘氨酸281→谷氨酸)

Uroporphyrinogen decarboxylase structural mutant (Gly281----Glu) in a case of porphyria.

作者信息

de Verneuil H, Grandchamp B, Beaumont C, Picat C, Nordmann Y

出版信息

Science. 1986 Nov 7;234(4777):732-4. doi: 10.1126/science.3775362.

Abstract

Uroporphyrinogen decarboxylase deficiency in man is responsible for familial porphyria cutanea tarda and hepatoerythropoietic porphyria. A recent study of a family with hepatoerythropoietic porphyria showed that the enzyme defect resulted from rapid degradation of the protein in vivo. Cloning and sequencing of a complementary DNA for the mutated gene revealed that the mutation was due to the replacement of a glycine residue by a glutamic acid residue at position 281. This base change leads to a protein that is very rapidly degraded in the presence of cell lysate. Characterization of the mutation will allow comparison of this defect in a homozygous patient with defects in other patients with familial porphyria cutanea tarda.

摘要

人类尿卟啉原脱羧酶缺乏可导致家族性迟发性皮肤卟啉症和肝红细胞生成性卟啉症。最近一项对患有肝红细胞生成性卟啉症的家族进行的研究表明,酶缺陷是由体内蛋白质的快速降解所致。对突变基因的互补DNA进行克隆和测序显示,该突变是由于281位的甘氨酸残基被谷氨酸残基取代。这种碱基变化导致一种蛋白质在细胞裂解液存在的情况下迅速降解。对该突变的特征描述将有助于将该纯合患者的这一缺陷与其他家族性迟发性皮肤卟啉症患者的缺陷进行比较。

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