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与血清高水平相关的细胞外超氧化物歧化酶基因的分子分析

Molecular analysis of extracellular-superoxide dismutase gene associated with high level in serum.

作者信息

Yamada H, Yamada Y, Adachi T, Goto H, Ogasawara N, Futenma A, Kitano M, Hirano K, Kato K

机构信息

First Department of Internal Medicine, Aichi Medical University, Japan.

出版信息

Jpn J Hum Genet. 1995 Jun;40(2):177-84. doi: 10.1007/BF01883574.

Abstract

Extracellular-superoxide dismutase (EC-SOD) is one of the SOD isozymes mainly distributed in the extracellular fluid. In the vascular system, it is located on the endothelial cell surface according to studies on the heparin binding capacity. By measurement of serum EC-SOD levels of Japanese in healthy persons (n = 103) and hemodialysis patients (n = 150), 7 healthy subjects and 24 hemodialysis patients were classified into group II associated with high EC-SOD levels. By molecular analysis of the EC-SOD coding region from the group II individuals in Sweden, a single nucleotide substitution of G to C generating an amino acid change of arginine to glycine has been identified in the region associated with the heparin affinity of the enzyme. The same mutation was detected in the Japanese as a homozygote in both alleles of 2 hemodialysis patients and as a heterozygote in one allele of all the healthy group II individuals and 17 hemodialysis patients. The amino acid substitution may result in the decrease of the heparin affinity which is favorable for the existence of EC-SOD in the serum.

摘要

细胞外超氧化物歧化酶(EC-SOD)是主要分布于细胞外液的超氧化物歧化酶同工酶之一。在血管系统中,根据对肝素结合能力的研究,它位于内皮细胞表面。通过检测健康日本人(n = 103)和血液透析患者(n = 150)的血清EC-SOD水平,7名健康受试者和24名血液透析患者被归类为与高EC-SOD水平相关的II组。通过对瑞典II组个体的EC-SOD编码区进行分子分析,在与该酶肝素亲和力相关的区域中,已鉴定出一个从G到C的单核苷酸取代,导致氨基酸从精氨酸变为甘氨酸。在日本人中,2名血液透析患者的两个等位基因均检测到该相同突变的纯合子,所有健康II组个体和17名血液透析患者的一个等位基因中检测到该相同突变的杂合子。氨基酸取代可能导致肝素亲和力降低,这有利于EC-SOD在血清中的存在。

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