Norbis F, Perego C, Markovich D, Stange G, Verri T, Murer H
University of Zürich, Institute of Physiology, Switzerland.
Pflugers Arch. 1994 Oct;428(3-4):217-23. doi: 10.1007/BF00724500.
We have isolated a cDNA (ileal NaSi-1) from rat small intestine by homology screening with a cDNA (renal NaSi-1) encoding rat kidney cortex Na(+)-SO4(2-) cotransport. Ileal NaSi-1 cRNA specifically stimulates Na(+)-dependent SO4(2-) uptake in a time- and dose-dependent manner in Xenopus laevis oocytes, with kinetic parameters almost identical to those of the renal NaSi-1. Ileal NaSi-1 cDNA contains 2722 base pairs (bp), almost 500 bp more than the renal NaSi-1 cDNA; however, it encodes a protein of 595 amino acids identical to the renal NaSi-1 protein. Northern blot analysis shows strong signals in rat lower small intestine and kidney cortex (2.9 x 10(3) and 2.3 x 10(3) bases), with the ileal NaSi-1 corresponding to the longer transcript. We conclude that we have identified a rat ileal cDNA that encodes a membrane protein most likely involved in brush-border Na(+)-SO4(2-) cotransport. It differs to the renal NaSi-1 only in the length of the 3' untranslated region, suggesting that the major difference lies in the differential use of polyadenylation signals.
我们通过与编码大鼠肾皮质Na(+)-SO4(2-)协同转运体的cDNA(肾NaSi-1)进行同源性筛选,从大鼠小肠中分离出了一个cDNA(回肠NaSi-1)。回肠NaSi-1的cRNA在非洲爪蟾卵母细胞中能以时间和剂量依赖的方式特异性刺激Na(+)-依赖的SO4(2-)摄取,其动力学参数与肾NaSi-1几乎相同。回肠NaSi-1的cDNA包含2722个碱基对(bp),比肾NaSi-1的cDNA多近500 bp;然而,它编码的是一个由595个氨基酸组成的与肾NaSi-1蛋白相同的蛋白质。Northern印迹分析显示在大鼠小肠下段和肾皮质中有强信号(2.9×10(3)和2.3×10(3)个碱基),回肠NaSi-1对应于较长的转录本。我们得出结论,我们鉴定出了一个大鼠回肠cDNA,它编码一种最有可能参与刷状缘Na(+)-SO4(2-)协同转运的膜蛋白。它与肾NaSi-1的差异仅在于3'非翻译区的长度,这表明主要差异在于多聚腺苷酸化信号的不同使用。