FXYD3 (Mat-8), a new regulator of Na,K-ATPase

被引:31
作者
Crambert, G [1 ]
Li, CM [1 ]
Claeys, D [1 ]
Geering, K [1 ]
机构
[1] Univ Lausanne, Dept Pharmacol & Toxicol, CH-1005 Lausanne, Switzerland
关键词
D O I
10.1091/mbc.E04-10-0878
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Four of the seven members of the FXYD protein family have been identified as specific regulators of Na,K-ATPase. In this study, we show that FXYD3, also known as Mat-8, is able to associate with and to modify the transport properties of Na,K-ATPase. In addition to this shared function, FXYD3 displays some uncommon characteristics. First, in contrast to other FXYD proteins, which were shown to be type I membrane proteins, FXYD3 may have a second transmembrane-like domain because of the presence of a noncleavable signal peptide. Second, FXYD3 can associate with Na,K- as well as H,K-ATPases when expressed in Xenopus oocytes. However, in situ (stomach), FXYD3 is associated only with Na,K-ATPase because its expression is restricted to mucous cells in which H,K-ATPase is absent. Coexpressed in Xenopus oocytes, FXYD3 modulates the glycosylation processing of the beta subunit of X,K-ATPase dependent on the presence of the signal peptide. Finally, FXYD3 decreases both the apparent affinity for Na+ and K+ of Na,K-ATPase.
引用
收藏
页码:2363 / 2371
页数:9
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