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泛素蛋白连接酶WWP2与上皮钠通道结合并使其下调。

Ubiquitin-protein ligase WWP2 binds to and downregulates the epithelial Na(+) channel.

作者信息

McDonald Fiona J, Western Andrea H, McNeil John D, Thomas Brittany C, Olson Diane R, Snyder Peter M

机构信息

Department of Physiology, University of Otago, Dunedin 9100, New Zealand.

出版信息

Am J Physiol Renal Physiol. 2002 Sep;283(3):F431-6. doi: 10.1152/ajprenal.00080.2002.

Abstract

The epithelial Na(+) channel (ENaC) is a critical component of the pathway maintaining salt and water balance. The channel is regulated by members of the Nedd4 family of ubiquitin-protein ligases, which bind to channel subunits and catalyze channel internalization and degradation. ENaC mutations that abolish this interaction cause Liddle's syndrome, a genetic form of hypertension. Here, we test the hypothesis that WW domain-containing protein 2 (WWP2), a member of the Nedd4 family of ubiquitin-protein ligases, is a candidate to regulate ENaC. Consistent with this hypothesis, we found that WWP2 is expressed in epithelial tissues that express ENaC, as well as in a wide variety of other tissues. WWP2 contains four WW domains, three of which bound differentially to ENaC subunits. In contrast, all four human Nedd4-2 WW domains bound to ENaC. WWP2 inhibited ENaC when coexpressed in epithelia, requiring a direct interaction between the proteins; mutation of the ENaC PY motifs abolished inhibition. Thus expression, binding, and functional data all suggest that WWP2 is a candidate to regulate ENaC-mediated Na(+) transport in epithelia.

摘要

上皮钠离子通道(ENaC)是维持盐和水平衡途径的关键组成部分。该通道受泛素蛋白连接酶Nedd4家族成员的调节,这些成员与通道亚基结合并催化通道内化和降解。消除这种相互作用的ENaC突变会导致利德尔综合征,这是一种遗传性高血压。在这里,我们测试了一个假设,即泛素蛋白连接酶Nedd4家族的成员含WW结构域蛋白2(WWP2)是调节ENaC的候选者。与该假设一致,我们发现WWP2在上皮组织中表达,这些上皮组织也表达ENaC,以及在多种其他组织中表达。WWP2包含四个WW结构域,其中三个与ENaC亚基有不同的结合。相比之下,人类所有四个Nedd4-2 WW结构域都与ENaC结合。当在上皮细胞中共表达时,WWP2抑制ENaC,这需要蛋白质之间的直接相互作用;ENaC PY基序的突变消除了抑制作用。因此,表达、结合和功能数据均表明WWP2是调节上皮细胞中ENaC介导的钠离子转运的候选者。

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