Macara I G
Center for Cell Signaling, University of Virginia, Charlottesville, Virginia 22908-0577, USA.
Microbiol Mol Biol Rev. 2001 Dec;65(4):570-94, table of contents. doi: 10.1128/MMBR.65.4.570-594.2001.
A defining characteristic of eukaryotic cells is the possession of a nuclear envelope. Transport of macromolecules between the nuclear and cytoplasmic compartments occurs through nuclear pore complexes that span the double membrane of this envelope. The molecular basis for transport has been revealed only within the last few years. The transport mechanism lacks motors and pumps and instead operates by a process of facilitated diffusion of soluble carrier proteins, in which vectoriality is provided by compartment-specific assembly and disassembly of cargo-carrier complexes. The carriers recognize localization signals on the cargo and can bind to pore proteins. They also bind a small GTPase, Ran, whose GTP-bound form is predominantly nuclear. Ran-GTP dissociates import carriers from their cargo and promotes the assembly of export carriers with cargo. The ongoing discovery of numerous carriers, Ran-independent transport mechanisms, and cofactors highlights the complexity of the nuclear transport process. Multiple regulatory mechanisms are also being identified that control cargo-carrier interactions. Circadian rhythms, cell cycle, transcription, RNA processing, and signal transduction are all regulated at the level of nucleocytoplasmic transport. This review focuses on recent discoveries in the field, with an emphasis on the carriers and cofactors involved in transport and on possible mechanisms for movement through the nuclear pores.
真核细胞的一个决定性特征是拥有核膜。大分子在细胞核和细胞质区室之间的运输通过跨越该膜双层的核孔复合体进行。运输的分子基础直到最近几年才被揭示。运输机制没有马达和泵,而是通过可溶性载体蛋白的易化扩散过程运作,其中方向性由货物 - 载体复合物的区室特异性组装和拆卸提供。载体识别货物上的定位信号并能与孔蛋白结合。它们还结合一种小GTP酶Ran,其GTP结合形式主要存在于细胞核中。Ran - GTP使输入载体与其货物解离,并促进输出载体与货物的组装。不断发现的众多载体、不依赖Ran的运输机制和辅助因子突出了核运输过程的复杂性。还发现了多种控制货物 - 载体相互作用的调节机制。昼夜节律、细胞周期、转录、RNA加工和信号转导都在核质运输水平上受到调节。本综述重点关注该领域的最新发现,重点是参与运输的载体和辅助因子以及通过核孔移动的可能机制。