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穿过核孔复合体的运输途径。

Transport routes through the nuclear pore complex.

作者信息

Pemberton L F, Blobel G, Rosenblum J S

机构信息

Laboratory of Cell Biology, Howard Hughes Medical Institute, Rockefeller University, New York, NY 10021, USA.

出版信息

Curr Opin Cell Biol. 1998 Jun;10(3):392-9. doi: 10.1016/s0955-0674(98)80016-1.

DOI:10.1016/s0955-0674(98)80016-1
PMID:9640541
Abstract

The nuclear pore complex can be considered to be the stationary phase of bidirectional traffic between the nucleus and the cytoplasm. The mobile phase consists of karyopherins, transport substrates, and the small GTPase Ran and its modulators. Recently, the family of karyopherins was expanded with the recognition of numerous open reading frames with limited homology to karyopherin beta 1. In several cases, the specific substrates transported by the new karyopherins have been identified, allowing the characterization of new pathways into and out of the nucleus. However, the mechanisms of transport, particularly the role of Ran, remain poorly understood.

摘要

核孔复合体可被视为细胞核与细胞质之间双向运输的固定阶段。流动相由核转运蛋白、运输底物、小GTP酶Ran及其调节剂组成。最近,随着众多与核转运蛋白β1具有有限同源性的开放阅读框被识别,核转运蛋白家族得以扩展。在一些情况下,已鉴定出新核转运蛋白运输的特定底物,从而能够对进出细胞核的新途径进行表征。然而,运输机制,尤其是Ran的作用,仍知之甚少。

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1
Transport routes through the nuclear pore complex.穿过核孔复合体的运输途径。
Curr Opin Cell Biol. 1998 Jun;10(3):392-9. doi: 10.1016/s0955-0674(98)80016-1.
2
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Receptor-mediated substrate translocation through the nuclear pore complex without nucleotide triphosphate hydrolysis.受体介导的底物通过核孔复合体的转运,无需三磷酸核苷酸水解。
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A novel class of RanGTP binding proteins.一类新型的RanGTP结合蛋白。
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A role for RanBP1 in the release of CRM1 from the nuclear pore complex in a terminal step of nuclear export.RanBP1在核输出的最后一步中从核孔复合体释放CRM1的过程中发挥作用。
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