Beck J T, Ullman B
J Biol Chem. 1987 Feb 15;262(5):2393-7.
A mutant cell line was selected from wild type S49 lymphoblasts that expressed a novel high affinity purine base transport system not found in parental cells or any other mammalian cell line (Aronow, B., Toll, D., Patrick, J., Hollingsworth, P., McCartan, K., and Ullman, B. (1986) Mol. Cell. Biol. 6, 2957-2962). In order to determine whether this nucleobase transport system was bidirectional, mutant cell lines possessing this high affinity base transport capability were derived from a nucleoside transport-deficient derivative of an adenylosuccinate synthetase-deficient S49 cell line. The resulting progeny excreted significantly greater amounts of purine into the cell culture medium than parental cells. This purine was identified as hypoxanthine. These results demonstrate genetically that the high affinity purine base transport system can mediate both the influx and efflux of hypoxanthine.
从野生型S49淋巴母细胞中筛选出一种突变细胞系,该细胞系表达了一种新型的高亲和力嘌呤碱转运系统,而亲代细胞或任何其他哺乳动物细胞系中均未发现这种系统(Aronow, B., Toll, D., Patrick, J., Hollingsworth, P., McCartan, K., and Ullman, B. (1986) Mol. Cell. Biol. 6, 2957 - 2962)。为了确定这种核碱基转运系统是否是双向的,具有这种高亲和力碱基转运能力的突变细胞系源自腺苷酸琥珀酸合成酶缺陷型S49细胞系的核苷转运缺陷衍生物。与亲代细胞相比,产生的子代细胞向细胞培养基中分泌的嘌呤量显著增加。这种嘌呤被鉴定为次黄嘌呤。这些结果从遗传学上证明,高亲和力嘌呤碱转运系统可以介导次黄嘌呤的流入和流出。