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由于酶反馈抗性突变导致的人类过量生产疾病。痛风中嘌呤过量产生是由于突变的反馈抗性磷酸核糖焦磷酸合成酶活性过高。

Overproduction disease in man due to enzyme feedback resistance mutation. Purine overproduction in gout due to excessive activity of mutant feedback-resistant phosphoribosylpyrophosphate synthetase.

作者信息

Sperling O, Boer P, Brosh S, Zoref E, de Vries A

出版信息

Enzyme. 1978;23(1):1-9. doi: 10.1159/000458543.

Abstract

Physiologically superactive phosphoribosylpyrophosphate (PRPP) synthetase, due to feedback resistance mutation, was found in a family with excessive purine production, gout and uric acid lithiasis. The superactivity of the mutant enzyme was manifest in the propositus' erythrocytes and cultured fibroblasts, in increased generation, content and metabolic availability of PRPP, leading in the fibroblasts to acceleration of the rate of purine synthesis de novo. One of the propositus' two siblings was similarly affected, but the propositus' father, his second brother and four sons, were all clinically and biochemically normal. The mother was clinically normal and normouricemic, but hyperuricosuric. Cultured fibroblasts from her skin exhibited variability in PRPP content and availability and in the rate of purine synthesis de novo. The mother's cultures were found to contain a mosaicism of two cell populations, one with normal and the other with mutant PRPP synthetase, indicating an X-linked pattern of inheritance of the PRPP synthetase abnormality in this gouty family.

摘要

在一个嘌呤产生过多、患有痛风和尿酸结石的家族中,发现了因反馈抗性突变导致的生理活性过高的磷酸核糖焦磷酸(PRPP)合成酶。突变酶的超活性在先证者的红细胞和培养的成纤维细胞中表现出来,表现为PRPP的生成增加、含量增加和代谢可用性增加,导致成纤维细胞中嘌呤从头合成速率加快。先证者的两个兄弟姐妹中有一个受到类似影响,但先证者的父亲、他的二哥和四个儿子在临床和生化方面均正常。母亲临床正常,血尿酸正常,但尿酸排泄过多。从她皮肤上培养的成纤维细胞在PRPP含量、可用性和嘌呤从头合成速率方面表现出变异性。发现母亲的培养物中含有两种细胞群体的嵌合体,一种具有正常的PRPP合成酶,另一种具有突变的PRPP合成酶,这表明在这个痛风家族中,PRPP合成酶异常的遗传模式为X连锁。

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