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奶牛中尿苷一磷酸合酶缺乏症:一种遗传性乳清酸尿症模型。

Deficiency of UMP synthase in dairy cattle: a model for hereditary orotic aciduria.

作者信息

Harden K K, Robinson J L

机构信息

Department of Animal Sciences, University of Illinois, Urbana 61801.

出版信息

J Inherit Metab Dis. 1987;10(3):201-9. doi: 10.1007/BF01800062.

Abstract

Deficiency of uridine-5'-monophosphate (UMP) synthase in dairy cattle, a condition analogous to human hereditary orotic aciduria, is reviewed with consideration of similarities and differences between the enzyme deficiency in humans and cattle. New findings regarding the bovine condition are reported including presence of the enzyme deficiency in numerous tissues and absence of substantial effects on other aspects of nucleotide metabolism. Specifically, erythrocyte concentration of phosphoribosylpyrophosphate (PRPP) and activities of PRPP synthetase, adenine phosphoribosyltransferase, and hypoxanthine-guanine phosphoribosyltransferase appear to be normal in cattle heterozygous for UMP synthase deficiency.

摘要

本文回顾了奶牛中尿苷-5'-单磷酸(UMP)合酶缺乏症,该病症类似于人类遗传性乳清酸尿症,同时考虑了人类和奶牛中酶缺乏症的异同。报告了关于牛这种病症的新发现,包括在许多组织中存在酶缺乏症,以及对核苷酸代谢的其他方面没有实质性影响。具体而言,对于UMP合酶缺乏症的杂合牛,红细胞中磷酸核糖焦磷酸(PRPP)的浓度以及PRPP合成酶、腺嘌呤磷酸核糖转移酶和次黄嘌呤-鸟嘌呤磷酸核糖转移酶的活性似乎正常。

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