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次黄嘌呤磷酸核糖转移酶缺陷型转基因小鼠培养神经元中尿苷三磷酸(UTP)和胞苷三磷酸(CTP)含量升高。

Elevated UTP and CTP content in cultured neurons from HPRT-deficient transgenic mice.

作者信息

Brosh S, Boer P, Sperling O, Zoref-Shani E

机构信息

Felsenstein Medical Research Center, Rabin Medical Center, Petah-Tikva, Israel.

出版信息

J Mol Neurosci. 2000 Feb-Apr;14(1-2):87-91. doi: 10.1385/JMN:14:1-2:087.

DOI:10.1385/JMN:14:1-2:087
PMID:10854040
Abstract

Hypoxanthine-guanine phosphoribosyltransferase (EC 2.4.2.8.; HPRT) catalyzes the salvage synthesis of inosine-5'-monophosphate (IMP) and guanosine-5'-monophosphate (GMP) from the purine bases hypoxanthine and guanine, respectively. Complete deficiency of HPRT activity is associated with the Lesch-Nyhan syndrome (LNS), characterized by excessive purine production and severe neurological manifestations. The etiology of the metabolic consequences of HPRT deficiency is clarified, but that of the neurological manifestations is not yet understood. HPRT-deficient mice represent an experimental animal model of LNS. In search for a possible metabolic abnormality in LNS brains, connecting the neurological deficit to HPRT deficiency, the purine and pyrimidine nucleotide content of cultured neurons, prepared from HPRT-deficient transgenic mice, was now determined. The HPRT-deficient neuronal cultures exhibited a significantly elevated content of the pyrimidine nucleotides UTP (1.33-fold the normal level, p = 0.0002) and CTP (1.28-fold the normal level, p = 0.02), but normal content of the purine nucleotides ATP and GTP. This abnormality in neuronal pyrimidine nucleotide content may be associated with the pathophysiology of the neurological deficit in LNS.

摘要

次黄嘌呤 - 鸟嘌呤磷酸核糖转移酶(EC 2.4.2.8.;HPRT)分别催化由嘌呤碱次黄嘌呤和鸟嘌呤补救合成5'-肌苷酸(IMP)和5'-鸟苷酸(GMP)。HPRT活性完全缺乏与莱施 - 奈恩综合征(LNS)相关,其特征是嘌呤产生过多和严重的神经学表现。HPRT缺乏的代谢后果的病因已明确,但神经学表现的病因尚不清楚。HPRT缺陷小鼠代表LNS的实验动物模型。为了寻找LNS大脑中可能存在的代谢异常,将神经功能缺陷与HPRT缺乏联系起来,现在测定了从HPRT缺陷转基因小鼠制备的培养神经元中的嘌呤和嘧啶核苷酸含量。HPRT缺陷的神经元培养物中嘧啶核苷酸UTP(为正常水平的1.33倍,p = 0.0002)和CTP(为正常水平的1.28倍,p = 0.02)含量显著升高,但嘌呤核苷酸ATP和GTP含量正常。神经元嘧啶核苷酸含量的这种异常可能与LNS神经功能缺陷的病理生理学有关。

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Elevated UTP and CTP content in cultured neurons from HPRT-deficient transgenic mice.次黄嘌呤磷酸核糖转移酶缺陷型转基因小鼠培养神经元中尿苷三磷酸(UTP)和胞苷三磷酸(CTP)含量升高。
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[Complete and partial deficiency of HPRT].[次黄嘌呤磷酸核糖转移酶的完全和部分缺乏]
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5
Production of a model for Lesch-Nyhan syndrome in hypoxanthine phosphoribosyltransferase-deficient mice.次黄嘌呤磷酸核糖基转移酶缺陷小鼠中莱施-奈恩综合征模型的构建。
Nat Genet. 1993 Mar;3(3):235-40. doi: 10.1038/ng0393-235.
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Functional analysis of brain dopamine systems in a genetic mouse model of Lesch-Nyhan syndrome.莱施-奈恩综合征基因小鼠模型中脑多巴胺系统的功能分析
J Pharmacol Exp Ther. 1992 Nov;263(2):596-607.
8
Lesch-Nyhan syndrome: mRNA expression of HPRT in patients with enzyme proven deficiency of HPRT and normal HPRT coding region of the DNA.Lesch-Nyhan 综合征:经酶证实存在 HPRT 缺乏但 HPRT 的 DNA 编码区正常的患者的 HPRT mRNA 表达。
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[Deficiencies of hypoxanthine guanine phosphoribosyltransferase (HPRT)].[次黄嘌呤鸟嘌呤磷酸核糖转移酶(HPRT)缺乏症]
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本文引用的文献

1
A FAMILIAL DISORDER OF URIC ACID METABOLISM AND CENTRAL NERVOUS SYSTEM FUNCTION.一种尿酸代谢与中枢神经系统功能的家族性疾病。
Am J Med. 1964 Apr;36:561-70. doi: 10.1016/0002-9343(64)90104-4.
2
Abnormal purine and pyrimidine nucleotide content in primary astroglia cultures from hypoxanthine-guanine phosphoribosyltransferase-deficient transgenic mice.次黄嘌呤 - 鸟嘌呤磷酸核糖转移酶缺陷型转基因小鼠原代星形胶质细胞培养物中嘌呤和嘧啶核苷酸含量异常。
J Neurochem. 1999 Mar;72(3):1139-45. doi: 10.1046/j.1471-4159.1999.0721139.x.
3
Developmental changes in purine nucleotide metabolism in cultured rat astroglia.
神经元分化过程中的嘌呤代谢:嘌呤合成和回收的相关性。
J Neurochem. 2013 Dec;127(6):805-18. doi: 10.1111/jnc.12366. Epub 2013 Aug 18.
4
Severe pyridine nucleotide depletion in fibroblasts from Lesch-Nyhan patients.莱施-奈恩综合征患者成纤维细胞中严重的吡啶核苷酸耗竭。
Biochem J. 2002 Aug 15;366(Pt 1):265-72. doi: 10.1042/BJ20020148.
培养的大鼠星形胶质细胞中嘌呤核苷酸代谢的发育变化
Int J Dev Neurosci. 1995 Dec;13(8):887-96. doi: 10.1016/0736-5748(95)00054-2.
4
Characterization of the alterations in purine nucleotide metabolism in hypoxanthine-guanine phosphoribosyltransferase-deficient rat neuroma cell line.次黄嘌呤-鸟嘌呤磷酸核糖基转移酶缺陷型大鼠神经瘤细胞系中嘌呤核苷酸代谢改变的特征分析
J Neurochem. 1993 Aug;61(2):457-63. doi: 10.1111/j.1471-4159.1993.tb02146.x.
5
Dopamine deficiency in a genetic mouse model of Lesch-Nyhan disease.莱施-奈恩病基因小鼠模型中的多巴胺缺乏
J Neurosci. 1994 Mar;14(3 Pt 1):1164-75. doi: 10.1523/JNEUROSCI.14-03-01164.1994.
6
Clinical, post-mortem, biochemical and therapeutic observations on the Lesch-Nyhan syndrome with particular reference to the Neurological manifestations.关于莱施-奈恩综合征的临床、尸检、生化及治疗观察,特别提及神经学表现。
Q J Med. 1982;51(201):43-78.
7
Biochemical evidence of dysfunction of brain neurotransmitters in the Lesch-Nyhan syndrome.莱施-奈恩综合征中脑内神经递质功能障碍的生化证据。
N Engl J Med. 1981 Nov 5;305(19):1106-11. doi: 10.1056/NEJM198111053051902.
8
Enzyme defect associated with a sex-linked human neurological disorder and excessive purine synthesis.与一种X连锁人类神经疾病及嘌呤过度合成相关的酶缺陷。
Science. 1967 Mar 31;155(3770):1682-4. doi: 10.1126/science.155.3770.1682.
9
The Lesch-Nyhan syndrome.莱施-奈恩综合征。
Annu Rev Med. 1973;24:41-60. doi: 10.1146/annurev.me.24.020173.000353.
10
Z-nucleotide accumulation in erythrocytes from Lesch-Nyhan patients.莱施-奈恩综合征患者红细胞中Z-核苷酸的积累。
J Clin Invest. 1985 Dec;76(6):2416-9. doi: 10.1172/JCI112255.