Nachury M V, Weis K
Department of Molecular and Cell Biology, University of California, Berkeley, CA 94729-3200, USA.
Proc Natl Acad Sci U S A. 1999 Aug 17;96(17):9622-7. doi: 10.1073/pnas.96.17.9622.
Transport of macromolecules across the nuclear envelope is an active process that depends on soluble factors including the GTPase Ran. Ran-GTP is predominantly located in the nucleus and has been shown to regulate cargo binding and release of import and export receptors in their respective target compartments. Recently, it was shown that transport of receptor-cargo complexes across the nuclear pore complex (NPC) does not depend on GTP-hydrolysis by Ran; however, the mechanism of translocation is still poorly understood. Here, we show that the direction of transport through the NPC can be inverted in the presence of high concentrations of cytoplasmic Ran-GTP. Under these conditions, two different classes of export cargoes are transported into the nucleus in the absence of GTP hydrolysis. The inverted transport is very rapid and can be blocked by known inhibitors of nuclear protein export. These results suggest that the NPC functions as a facilitated transport channel, allowing the selective translocation of receptor-cargo complexes. We conclude that the directionality of nucleocytoplasmic transport is determined mainly by the compartmentalized distribution of Ran-GTP.
大分子穿过核膜的运输是一个活跃的过程,它依赖于包括GTP酶Ran在内的可溶性因子。Ran-GTP主要位于细胞核中,并且已被证明可调节货物在各自目标区室中与进出口受体的结合和释放。最近有研究表明,受体-货物复合物穿过核孔复合体(NPC)的运输并不依赖于Ran的GTP水解;然而,转运机制仍知之甚少。在这里,我们表明,在高浓度细胞质Ran-GTP存在的情况下,通过NPC的运输方向可以反转。在这些条件下,两类不同的输出货物在没有GTP水解的情况下被转运到细胞核中。这种反向运输非常迅速,并且可以被已知的核蛋白输出抑制剂阻断。这些结果表明,NPC作为一个易化运输通道,允许受体-货物复合物进行选择性转运。我们得出结论,核质运输的方向性主要由Ran-GTP的区室化分布决定。