Crambert Gilles, Li Ciming, Claeys Dirk, Geering Käthi
Department of Pharmacology and Toxicology, University of Lausanne, CH-1005 Lausanne, Switzerland.
Mol Biol Cell. 2005 May;16(5):2363-71. doi: 10.1091/mbc.e04-10-0878. Epub 2005 Mar 2.
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.
FXYD蛋白家族的七个成员中有四个已被确定为钠钾ATP酶的特异性调节剂。在本研究中,我们发现FXYD3(也称为Mat-8)能够与钠钾ATP酶结合并改变其转运特性。除了这种共同功能外,FXYD3还表现出一些不寻常的特征。首先,与其他已被证明为I型膜蛋白的FXYD蛋白不同,由于存在不可切割的信号肽,FXYD3可能有第二个类似跨膜的结构域。其次,当在非洲爪蟾卵母细胞中表达时,FXYD3可以与钠钾ATP酶以及氢钾ATP酶结合。然而,在原位(胃)中,FXYD3仅与钠钾ATP酶结合,因为其表达仅限于不存在氢钾ATP酶的黏液细胞。在非洲爪蟾卵母细胞中共表达时,FXYD3会根据信号肽的存在调节氢钾ATP酶β亚基的糖基化加工。最后,FXYD3降低了钠钾ATP酶对钠离子和钾离子的表观亲和力。