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利用一种可传播的逆转录病毒载体对人类莱施-尼汉氏病(次黄嘌呤-鸟嘌呤磷酸核糖转移酶缺陷)淋巴母细胞进行部分表型校正。

Partial phenotypic correction of human Lesch-Nyhan (hypoxanthine-guanine phosphoribosyltransferase-deficient) lymphoblasts with a transmissible retroviral vector.

作者信息

Willis R C, Jolly D J, Miller A D, Plent M M, Esty A C, Anderson P J, Chang H C, Jones O W, Seegmiller J E, Friedmann T

出版信息

J Biol Chem. 1984 Jun 25;259(12):7842-9.

PMID:6203897
Abstract

A human Lesch-Nyhan (hereditary, severe hypoxanthine-guanine phosphoribosyltransferase (HPR transferase) deficiency) B-lymphoblast line was infected with an amphotropic retroviral vector containing human HPR transferase cDNA under transcriptional control of viral long terminal repeat sequences. Of 17 clones isolated, 12 integration groups were defined by analysis of restriction enzyme digests of their genomic DNA with HPR transferase and viral long terminal repeat probes. These groups had HPR transferase activity restored to levels of 4 to 23% of normal values. Aberrant metabolic parameters associated with severe deficiency of HPR transferase activity, i.e. elevated rates of purine excretion, increased accumulation of hypoxanthine, elevated 5-phosphoribosyl-1-pyrophosphate contents, altered nucleoside triphosphate pools, resistance to toxic effects of 6-thioguanine, were partially to nearly completely corrected; the degree of correction generally corresponded to the degree of restoration of HPR transferase activity. The integration of the HPR transferase gene was found to be variably stable during 9 months of culture of the virally transformed lymphoblasts under nonselective conditions. The HPR transferase gene-infected lines reverted to resistance to 20 microM 6-thioguanine, i.e. severe HPR transferase deficiency, at frequencies of 10(-6) to in excess of 10(-5) per generation. The reversions were accompanied by either a loss or rearrangement of the integrated HPR transferase sequences or by retention of the sequences in an unaltered form.

摘要

用人源莱施-奈恩综合征(遗传性严重次黄嘌呤-鸟嘌呤磷酸核糖转移酶(HPR转移酶)缺乏症)B淋巴细胞系,用一种嗜异性逆转录病毒载体进行感染,该载体含有在病毒长末端重复序列转录控制下的人HPR转移酶cDNA。在分离出的17个克隆中,通过用HPR转移酶和病毒长末端重复序列探针分析其基因组DNA的限制性酶切片段,确定了12个整合组。这些组的HPR转移酶活性恢复到正常值的4%至23%。与HPR转移酶活性严重缺乏相关的异常代谢参数,即嘌呤排泄率升高、次黄嘌呤积累增加、5-磷酸核糖-1-焦磷酸含量升高、核苷三磷酸库改变、对6-硫鸟嘌呤毒性作用的抗性,部分至几乎完全得到纠正;纠正程度一般与HPR转移酶活性的恢复程度相对应。发现在非选择性条件下对病毒转化的淋巴细胞进行9个月培养期间,HPR转移酶基因的整合稳定性各不相同。HPR转移酶基因感染的细胞系以每代10^(-6)至超过10^(-5)的频率恢复对20微摩尔6-硫鸟嘌呤的抗性,即严重HPR转移酶缺乏。这些回复伴随着整合的HPR转移酶序列的丢失或重排,或者序列以未改变的形式保留。

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