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一名具有莱施-奈恩综合征特征的聪明、未致残患者中一种次黄嘌呤-鸟嘌呤磷酸核糖转移酶(HPRT)变体对嘌呤的利用情况。

Utilization of purines by an HPRT variant in an intelligent, nonmutilative patient with features of the Lesch-Nyhan syndrome.

作者信息

Bakay B, Nissinen E, Sweetman L, Francke U, Nyhan W L

出版信息

Pediatr Res. 1979 Dec;13(12):1365-70. doi: 10.1203/00006450-197912000-00013.

Abstract

The patient, H.Chr.B., was among the first reported with hyperuricemia and central nervous system symptoms. He has been found to have a variant of hypoxanthine guanine phosphoribosyl transferase (HPRT; E.C.2.4.2.8) distinct from the enzyme present in patients with the Lesch-Nyhan syndrome. The patient had chroeoathetosis, spasticity, dysarthric speech, and hyperuricemia. However, his intelligence was normal and he had no evidence of self-mutilation. There was no activity of HPRT in the lysates of erythrocytes and cultured fibroblasts when analyzed in the usual manner. Using a newly developed method for the study of purine metabolism in intact cultured cells, this patient was found to metabolize some 9% of 8-14C-hypoxanthine, and 90% of the isotope utilized was converted to adenine and guanine nucleotides. In contrast, cells from patients with the Lesch-Nyhan syndrome were virtually completely unable to convert hypoxanthine to nucleotides. The patient's fibroblasts were even more efficient in the metabolism of 8-14C-guanine, which was utilized to the extent of 27%, over 80% of which was converted to guanine and adenine nucleotides. The growth of the cultured fibroblasts of this patient was intermediate in media containing hypoxanthine aminopterin thymidine (HAT), whereas the growth of Lesch-Nyhan cells was inhibited and normal cells grew normally. Similarly in 8-azaguanine, 6-thioguanine, and 8-azahypoxanthine, the growth of the patient's cells was intermediate between normal and Lesch-Nyhan cells. These observations provide further evidence for genetic heterogeneity among patients with disorders in purine metabolism involving the HPRT gene. They document that this famous patient did not have the Lesch-Nyhan syndrome.

摘要

患者H.Chr.B.是首批被报道患有高尿酸血症和中枢神经系统症状的病例之一。已发现他的次黄嘌呤鸟嘌呤磷酸核糖转移酶(HPRT;E.C.2.4.2.8)存在一种变体,与莱施-尼汉综合征患者体内的酶不同。该患者患有舞蹈徐动症、痉挛、构音障碍和高尿酸血症。然而,他智力正常,没有自残迹象。按照常规方法分析时,红细胞和培养的成纤维细胞裂解物中没有HPRT活性。使用一种新开发的研究完整培养细胞中嘌呤代谢的方法,发现该患者能代谢约9%的8-¹⁴C-次黄嘌呤,所利用的同位素中90%转化为腺嘌呤和鸟嘌呤核苷酸。相比之下,莱施-尼汉综合征患者的细胞几乎完全无法将次黄嘌呤转化为核苷酸。该患者的成纤维细胞在8-¹⁴C-鸟嘌呤的代谢方面效率更高,其利用率达27%,其中超过80%转化为鸟嘌呤和腺嘌呤核苷酸。在含有次黄嘌呤氨基蝶呤胸腺嘧啶核苷(HAT)的培养基中,该患者培养的成纤维细胞生长情况处于中等水平,而莱施-尼汉综合征患者细胞的生长受到抑制,正常细胞则正常生长。同样,在8-氮杂鸟嘌呤、6-硫鸟嘌呤和8-氮杂次黄嘌呤中,该患者细胞的生长情况介于正常细胞和莱施-尼汉综合征患者细胞之间。这些观察结果为涉及HPRT基因的嘌呤代谢紊乱患者之间的遗传异质性提供了进一步证据。它们证明这位著名患者并未患莱施-尼汉综合征。

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