Werner A, Biber J, Forgo J, Palacin M, Murer H
Department of Physiology, University of Zürich, Switzerland.
J Biol Chem. 1990 Jul 25;265(21):12331-6.
As a first step within an experimental strategy (expression cloning) leading to the structural identification of the two brush-border membrane transport systems for phosphate and sulfate, we have studied the expression of Na(+)-dependent uptake of phosphate and sulfate in Xenopus laevis oocytes injected with rabbit kidney cortex poly(A)+ RNA (mRNA). Na(+)-dependent uptake of phosphate and sulfate was stimulated in a dose- and time-dependent manner up to 20-fold as compared to water-injected controls. After fractionation of the mRNA on a sucrose gradient (or by preparative gel electrophoresis), two neighboring fractions were identified to stimulate Na(+)-dependent phosphate uptake (average size: 3.4 kilobases) and Na(+)-dependent sulfate uptake (average size: 3.7 kilobases). The two transport systems can be discriminated by their inhibition by thiosulfate, which reduced sulfate uptake, but not phosphate uptake. Kinetic characterization of the expressed Na(+)-dependent transport activities results in properties similar to those described for transport activity in renal brush-border membrane vesicles.
作为一种实验策略(表达克隆)的第一步,该策略旨在从结构上鉴定两种用于磷酸盐和硫酸盐的刷状缘膜转运系统,我们研究了注射兔肾皮质多聚腺苷酸加尾RNA(mRNA)的非洲爪蟾卵母细胞中钠依赖性磷酸盐和硫酸盐摄取的表达情况。与注射水的对照相比,钠依赖性磷酸盐和硫酸盐摄取以剂量和时间依赖性方式受到刺激,最高可达20倍。在蔗糖梯度上(或通过制备性凝胶电泳)对mRNA进行分级分离后,鉴定出两个相邻级分可刺激钠依赖性磷酸盐摄取(平均大小:3.4千碱基)和钠依赖性硫酸盐摄取(平均大小:3.7千碱基)。这两种转运系统可以通过硫代硫酸盐对它们的抑制作用来区分,硫代硫酸盐会降低硫酸盐摄取,但不会降低磷酸盐摄取。对表达的钠依赖性转运活性进行动力学表征,结果显示其性质与肾刷状缘膜囊泡中描述的转运活性相似。