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首页> 外文期刊>The biochemical journal >Roles of 14-3-3 and calmodulin binding in subcellular localization and function of the small G-protein Rem2
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Roles of 14-3-3 and calmodulin binding in subcellular localization and function of the small G-protein Rem2

机译:14-3-3和钙调蛋白结合在小G蛋白Rem2的亚细胞定位和功能中的作用

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pkir/Gem, Rad, Rem and Rem2 comprise the RGK (Rad/Gem/kir) family of Ras-related small G-proteins. Two important functions of RGK proteins are the regulation of the VDCC (voltage-dependent Casup2+/sup channel) activity and cell-shape remodelling. RGK proteins interact with 14-3-3 and CaM (calmodulin), but their role on RGK protein function is poorly understood. In contrast with the other RGK family members, Rem2 has been reported to bind neither 14-3-3 nor induce membrane extensions. Furthermore, although Rem2 inhibits VDCC activity, it does not prevent cell-surface transport of Casup2+/sup channels as has been shown for kir/Gem. In the present study, we re-examined the functions of Rem2 and its interaction with 14-3-3 and CaM. We show that Rem2 in fact does interact with 14-3-3 and CaM and induces dendrite-like extensions in COS cells. 14-3-3, together with CaM, regulates the subcellular distribution of Rem2 between the cytoplasm and the nucleus. Rem2 also interacts with the β-subunits of VDCCs in a GTP-dependent fashion and inhibits Casup2+/sup channel activity by blocking the α-subunit expression at the cell surface. Thus Rem2 shares many previously unrecognized features with the other RGK family members./p
机译:kir / Gem,Rad,Rem和Rem2组成与Ras相关的小G蛋白的RGK(Rad / Gem / kir)家族。 RGK蛋白的两个重要功能是调节VDCC(电压依赖性Ca 2 + 通道)活性和细胞形状重塑。 RGK蛋白与14-3-3和CaM(钙调蛋白)相互作用,但对它们在RGK蛋白功能上的作用了解甚少。与其他RGK家族成员相反,据报道Rem2既不结合14-3-3也不诱导膜延伸。此外,尽管Rem2抑制了VDCC活性,但是它并未像针对kir / Gem所示的那样阻止Ca 2 + 通道的细胞表面转运。在本研究中,我们重新检查了Rem2的功能及其与14-3-3和CaM的相互作用。我们显示,Rem2实际上确实与14-3-3和CaM相互作用,并在COS细胞中诱导树突状延伸。 14-3-3与CaM一起调节Rem2在细胞质和细胞核之间的亚细胞分布。 Rem2还以GTP依赖的方式与VDCC的β亚基相互作用,并通过阻断细胞表面的α亚基表达来抑制Ca 2 + 通道活性。因此Rem2与RGK家族的其他成员共享许多以前无法识别的功能。

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