Van Impe Katrien, Hubert Thomas, De Corte Veerle, Vanloo Berlinda, Boucherie Ciska, Vandekerckhove Joël, Gettemans Jan
Department of Medical Protein Research, VIB, B-9000 Ghent, Belgium.
Traffic. 2008 May;9(5):695-707. doi: 10.1111/j.1600-0854.2008.00720.x. Epub 2008 Feb 7.
The small GTPase Ran plays a central role in nucleocytoplasmic transport. Nuclear transport of Ran itself depends on nuclear transport factor 2 (NTF2). Here, we report that NTF2 and Ran control nuclear import of the filamentous actin capping protein CapG. In digitonin-permeabilized cells, neither GTPgammaS nor the GTP hydrolysis-deficient Ran mutant RanQ69L affect transit of CapG to the nucleus in the presence of cytosol. Obstruction of nucleoporins prevents nuclear transport of CapG, and we show that CapG binds to nucleoporin62. In addition, CapG interacts with NTF2, associates with Ran and is furthermore able to bind the NTF2-Ran complex. NTF2-Ran interaction is required for CapG nuclear import. This is corroborated by a NTF2 mutant with reduced affinity for Ran and a Ran mutant that does not bind NTF2, both of which prevent CapG import. Thus, a ubiquitously expressed protein shuttles to the nucleus through direct association with NTF2 and Ran. The role of NTF2 may therefore not be solely confined to sustaining the Ran gradient in cells.
小GTP酶Ran在核质运输中起核心作用。Ran自身的核运输依赖于核运输因子2(NTF2)。在此,我们报告NTF2和Ran控制丝状肌动蛋白封端蛋白CapG的核输入。在洋地黄皂苷通透的细胞中,在存在胞质溶胶的情况下,GTPγS和GTP水解缺陷型Ran突变体RanQ69L均不影响CapG向细胞核的转运。核孔蛋白的阻断会阻止CapG的核运输,并且我们表明CapG与核孔蛋白62结合。此外,CapG与NTF2相互作用,与Ran缔合,并且还能够结合NTF2-Ran复合物。CapG核输入需要NTF2-Ran相互作用。对Ran亲和力降低的NTF2突变体和不结合NTF2的Ran突变体均证实了这一点,两者均阻止CapG的输入。因此,一种普遍表达的蛋白质通过与NTF2和Ran直接缔合穿梭至细胞核。因此,NTF2的作用可能不仅限于维持细胞中的Ran梯度。