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The C-Terminal Tail of the Polycystin-1 Protein Interacts with the Na,K-ATPase α-Subunit

机译:Polycystin-1蛋白的C末端与Na,K-ATPaseα亚基相互作用

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摘要

Polycystin-1 (PC-1) is the product of the PKD1 gene, which is mutated in autosomal dominant polycystic kidney disease. We show that the Na,K-ATPase α-subunit interacts in vitro and in vivo with the final 200 amino acids of the polycystin-1 protein, which constitute its cytoplasmic C-terminal tail. Functional studies suggest that this association may play a role in the regulation of the Na,K-ATPase activity. Chinese hamster ovary cells stably expressing the entire PC-1 protein exhibit a dramatic increase in Na,K-ATPase activity, although the kinetic properties of the enzyme remain unchanged. These data indicate that polycystin-1 may contribute to the regulation of Na,K-ATPase activity in kidneys in situ, thus modulating renal tubular fluid and electrolyte transport.
机译:Polycystin-1(PC-1)是PKD1基因的产物,该基因在常染色体显性多囊肾疾病中发生突变。我们显示,Na,K-ATPaseα亚基在体外和体内与多囊藻蛋白1蛋白的最后200个氨基酸相互作用,这构成了它的细胞质C末端尾巴。功能研究表明,这种联系可能在Na,K-ATPase活性的调节中起作用。稳定表达整个PC-1蛋白的中国仓鼠卵巢细胞显示Na,K-ATPase活性显着增加,尽管该酶的动力学特性保持不变。这些数据表明,polycystin-1可能有助于调节肾脏中Na,K-ATPase的活性,从而调节肾小管的液体和电解质的运输。

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