Jia Z P, McCullough N, Wong L, Young P G
Department of Biology, Queen's University, Kingston, Ontario, Canada.
Mol Gen Genet. 1993 Nov;241(3-4):298-304. doi: 10.1007/BF00284681.
Amiloride, an inhibitor of various sodium transporters, is toxic to Schizosaccharomyces pombe at low concentration in minimal but not in rich media. Amiloride-resistant mutants were isolated and shown to represent a new locus (car1 for changed amiloride resistance) on chromosome I. The car1 gene was cloned and sequenced. Sequence analysis revealed an open reading frame of 526 amino acids with a predicted molecular weight of 58,545 Da. It has 52% hydrophobic residues and belongs to the class of 12-transmembrane-domain transport proteins. Gene disruption of car1 results in increased amiloride resistance. car1 has sequence similarity to proteins from Candida associated with resistance to benomyl, methotrexate and cycloheximide. No single physiologically identifiable component of sodium transport appeared to be lost. We propose that car1 serves an uptake function, perhaps as a symport with an unknown substrate and this carrier may transport amiloride into the cell. Further, we suggest that amiloride toxicity at low concentrations is not due to its effect on sodium transport but, rather, depends on intracellular interference with an unknown biosynthetic pathway.
氨氯吡咪是多种钠转运蛋白的抑制剂,在低浓度时对粟酒裂殖酵母有毒性,在基本培养基中如此,但在丰富培养基中则不然。分离出了氨氯吡咪抗性突变体,结果表明其代表位于第一条染色体上的一个新基因座(car1,即改变的氨氯吡咪抗性基因座)。克隆并测序了car1基因。序列分析揭示了一个由526个氨基酸组成的开放阅读框,预测分子量为58,545道尔顿。它有52%的疏水残基,属于12跨膜结构域转运蛋白类别。car1基因的破坏导致氨氯吡咪抗性增加。car1与白色念珠菌中与对苯菌灵、甲氨蝶呤和环己酰亚胺抗性相关的蛋白质具有序列相似性。钠转运的单一生理可识别成分似乎没有丢失。我们提出car1具有摄取功能,可能作为与未知底物的同向转运体,并且这种载体可能将氨氯吡咪转运到细胞中。此外,我们认为低浓度时氨氯吡咪的毒性并非因其对钠转运的作用,而是取决于对未知生物合成途径的细胞内干扰。