Moroianu J
Department of Biology, Boston College, Chestnut Hill, MA 02467, USA.
Crit Rev Eukaryot Gene Expr. 1999;9(2):89-106. doi: 10.1615/critreveukargeneexpr.v9.i2.10.
Molecules enter and exit the nucleus of eukaryotic cells through aqueous channels formed in the nuclear envelope by nuclear pore complexes (NPC). Proteins entering or leaving the nucleus use nuclear localization signals (NLSs), or nuclear export signals (NESs), respectively. Different types of NLSs and NESs are specifically recognized directly, or indirectly via adapters, by transport receptors. In recent years, many transport receptors, adapters, and the specific cargoes they carry into or out of the nucleus have been identified, revealing an increasing level of complexity. All the transport receptors identified are members of the same family and have in common the ability to shuttle between the nucleus and cytoplasm, and to interact with RanGTP and with nucleoporins at the NPC. The GTPase Ran regulates the interaction between receptors and cargoes, or adapters, and is crucial in providing directionality to nuclear import and export. One of the challenges for the future will be establishing the mechanisms of translocation through the NPC of receptors together with their cargoes. Nuclear import and export of many cargoes is regulated. The molecular mechanisms of regulation of nucleocytoplasmic transport during cell growth, development, viral infections, and different diseases constitute important areas of investigation.
分子通过核孔复合体(NPC)在核膜上形成的水性通道进出真核细胞的细胞核。进入或离开细胞核的蛋白质分别使用核定位信号(NLS)或核输出信号(NES)。不同类型的NLS和NES分别被转运受体直接或通过衔接蛋白间接特异性识别。近年来,许多转运受体、衔接蛋白以及它们携带进出细胞核的特定货物已被鉴定出来,揭示了越来越高的复杂性。所有已鉴定的转运受体都是同一家族的成员,它们的共同之处在于能够在细胞核和细胞质之间穿梭,并与RanGTP以及NPC处的核孔蛋白相互作用。GTP酶Ran调节受体与货物或衔接蛋白之间的相互作用,并且在为核输入和输出提供方向性方面至关重要。未来的挑战之一将是确定受体与其货物一起通过NPC转运的机制。许多货物的核输入和输出受到调控。细胞生长、发育、病毒感染和不同疾病期间核质运输调控的分子机制构成了重要的研究领域。