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[尿素循环障碍的分子基础]

[Molecular basis of urea cycle disorders].

作者信息

Matsuda I, Matsuura T, Hoshide R, Uchino T, Matsubasa T

机构信息

Department of Pediatrics, Kumamoto University School of Medicine.

出版信息

Nihon Rinsho. 1993 Feb;51(2):520-4.

PMID:8464164
Abstract

Five different enzymes, carbamyl phosphate synthetase I (CPS I), ornithine transcarbamylase (OTC) argininosuccinate synthetase (AS), argininosuccinate lyase (AL) and arginase (AR) play a role in urea synthesis from ammonium. The structures of cDNA of all these enzymes and those of genome DNA of some enzymes (OTC, AL, AR) have been already clarified, and using of the information, the alleles of each enzyme deficiency have been identified. Alleles are extremely heterogeneous in all enzyme deficiencies, in sharp difference from other inborn errors of metabolism, such as cystic fibrosis and hemoglobinopathies.

摘要

五种不同的酶,即氨甲酰磷酸合成酶I(CPS I)、鸟氨酸转氨甲酰酶(OTC)、精氨琥珀酸合成酶(AS)、精氨琥珀酸裂解酶(AL)和精氨酸酶(AR)在由铵合成尿素的过程中发挥作用。所有这些酶的cDNA结构以及某些酶(OTC、AL、AR)的基因组DNA结构均已阐明,利用这些信息,已鉴定出每种酶缺乏症的等位基因。在所有酶缺乏症中,等位基因具有极高的异质性,这与其他先天性代谢缺陷,如囊性纤维化和血红蛋白病形成鲜明差异。

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