The direction of transport through the nuclear pore can be inverted

被引:153
作者
Nachury, MV [1 ]
Weis, K [1 ]
机构
[1] Univ Calif Berkeley, Dept Mol & Cell Biol, Berkeley, CA 94729 USA
关键词
D O I
10.1073/pnas.96.17.9622
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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; holt;ever, the mechanism of translocation is still poorly understood. Were, 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.
引用
收藏
页码:9622 / 9627
页数:6
相关论文
共 35 条
  • [11] A 41 amino acid motif in importin-alpha confers binding to importin-beta and hence transit into the nucleus
    Gorlich, D
    Henklein, P
    Laskey, RA
    Hartmann, E
    [J]. EMBO JOURNAL, 1996, 15 (08) : 1810 - 1817
  • [12] Identification of different roles for RanGDP and RanGTP in nuclear protein import
    Gorlich, D
    Pante, N
    Kutay, U
    Aebi, U
    Bischoff, FR
    [J]. EMBO JOURNAL, 1996, 15 (20) : 5584 - 5594
  • [13] The asymmetric distribution of the constituents of the Ran system is essential for transport into and out of the nucleus
    Izaurralde, E
    Kutay, U
    vonKobbe, C
    Mattaj, IW
    Gorlich, D
    [J]. EMBO JOURNAL, 1997, 16 (21) : 6535 - 6547
  • [14] The receptor Msn5 exports the phosphorylated transcription factor Pho4 out of the nucleus
    Kaffman, A
    Rank, NM
    O'Neill, EM
    Huang, LS
    O'Shea, EK
    [J]. NATURE, 1998, 396 (6710) : 482 - 486
  • [15] INTERACTION OF THE NUCLEAR GTP-BINDING PROTEIN RAN WITH ITS REGULATORY PROTEINS RCC1 AND RANGAP1
    KLEBE, C
    BISCHOFF, FR
    PONSTINGL, H
    WITTINGHOFER, A
    [J]. BIOCHEMISTRY, 1995, 34 (02) : 639 - 647
  • [16] Ran-unassisted nuclear migration of a 97-kD component of nuclear pore-targeting complex
    Kose, S
    Imamoto, N
    Tachibana, T
    Shimamoto, T
    Yoneda, Y
    [J]. JOURNAL OF CELL BIOLOGY, 1997, 139 (04) : 841 - 849
  • [17] Identification of a tRNA-specific nuclear export receptor
    Kutay, U
    Lipowsky, G
    Izaurralde, E
    Bischoff, FR
    Schwarzmaier, P
    Hartmann, E
    Gorlich, D
    [J]. MOLECULAR CELL, 1998, 1 (03) : 359 - 369
  • [18] Export of importin alpha from the nucleus is mediated by a specific nuclear transport factor
    Kutay, U
    Bischoff, FR
    Kostka, S
    Kraft, R
    Gorlich, D
    [J]. CELL, 1997, 90 (06) : 1061 - 1071
  • [19] Dominant-negative mutants of importin-beta block multiple pathways of import and export through the nuclear pore complex
    Kutay, U
    Izaurralde, E
    Bischoff, FR
    Mattaj, IW
    Gorlich, D
    [J]. EMBO JOURNAL, 1997, 16 (06) : 1153 - 1163
  • [20] Nucleocytoplasmic transport: The soluble phase
    Mattaj, IW
    Englmeier, L
    [J]. ANNUAL REVIEW OF BIOCHEMISTRY, 1998, 67 : 265 - 306