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本文引用的文献

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Importin 13: a novel mediator of nuclear import and export.输入蛋白13:一种新型的核输入与输出介质
EMBO J. 2001 Jul 16;20(14):3685-94. doi: 10.1093/emboj/20.14.3685.
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Ran-binding protein 3 is a cofactor for Crm1-mediated nuclear protein export.Ran结合蛋白3是Crm1介导的核蛋白输出的辅助因子。
J Cell Biol. 2001 Jun 25;153(7):1391-402. doi: 10.1083/jcb.153.7.1391.
3
Chromatin docking and exchange activity enhancement of RCC1 by histones H2A and H2B.组蛋白H2A和H2B对RCC1染色质对接和交换活性的增强作用
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Structural basis for guanine nucleotide exchange on Ran by the regulator of chromosome condensation (RCC1).染色体凝聚调节因子(RCC1)对Ran进行鸟嘌呤核苷酸交换的结构基础。
Cell. 2001 Apr 20;105(2):245-55. doi: 10.1016/s0092-8674(01)00315-4.
5
Inhibition of nuclear import by protein kinase B (Akt) regulates the subcellular distribution and activity of the forkhead transcription factor AFX.蛋白激酶B(Akt)对核输入的抑制作用调节了叉头转录因子AFX的亚细胞分布和活性。
Mol Cell Biol. 2001 May;21(10):3534-46. doi: 10.1128/MCB.21.10.3534-3546.2001.
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Nuclear export of 60s ribosomal subunits depends on Xpo1p and requires a nuclear export sequence-containing factor, Nmd3p, that associates with the large subunit protein Rpl10p.60S核糖体亚基的核输出依赖于Xpo1p,并需要一个含核输出序列的因子Nmd3p,该因子与大亚基蛋白Rpl10p相关联。
Mol Cell Biol. 2001 May;21(10):3405-15. doi: 10.1128/MCB.21.10.3405-3415.2001.
7
Nuclear import of histone H2A and H2B is mediated by a network of karyopherins.组蛋白H2A和H2B的核输入由核转运蛋白网络介导。
J Cell Biol. 2001 Apr 16;153(2):251-62. doi: 10.1083/jcb.153.2.251.
8
The karyopherin Kap142p/Msn5p mediates nuclear import and nuclear export of different cargo proteins.核转运蛋白Kap142p/Msn5p介导不同货物蛋白的核输入和核输出。
J Cell Biol. 2001 Feb 19;152(4):729-40. doi: 10.1083/jcb.152.4.729.
9
Gradient of increasing affinity of importin beta for nucleoporins along the pathway of nuclear import.在核输入途径中,输入蛋白β对核孔蛋白的亲和力沿该途径增加的梯度。
J Cell Biol. 2001 Jan 22;152(2):411-7. doi: 10.1083/jcb.152.2.411.
10
Prediction of structural domains of TAP reveals details of its interaction with p15 and nucleoporins.TAP结构域的预测揭示了其与p15和核孔蛋白相互作用的细节。
EMBO Rep. 2000 Jul;1(1):53-8. doi: 10.1093/embo-reports/kvd009.

进出细胞核。

Transport into and out of the nucleus.

作者信息

Macara I G

机构信息

Center for Cell Signaling, University of Virginia, Charlottesville, Virginia 22908-0577, USA.

出版信息

Microbiol Mol Biol Rev. 2001 Dec;65(4):570-94, table of contents. doi: 10.1128/MMBR.65.4.570-594.2001.

DOI:10.1128/MMBR.65.4.570-594.2001
PMID:11729264
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC99041/
Abstract

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.

摘要

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。