Mapping interactions between nuclear transport factors in living cells reveals pathways through the nuclear pore complex

被引:118
作者
Damelin, M [1 ]
Silver, PA [1 ]
机构
[1] Harvard Univ, Sch Med, Dana Farber Canc Inst, Dept Biol Chem & Mol Pharmacol, Boston, MA 02115 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1016/S1097-2765(00)80409-8
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The interactions between transport receptors and proteins of the nuclear pore complex (NPC) are fundamental to understanding nucleocytoplasmic transport. In order to delineate the path that a particular transport receptor takes through the NPC, we have employed fluorescence resonance energy transfer (FRET) between enhanced cyan and yellow fluorescent proteins (ECFP, EYFP) in living cells. A panel of yeast strains expressing functional receptor-ECFP and nucleoporin-EYFP fusions has been analyzed with a FRET assay. With this approach, we define points of contact in the NPC for the related importin Pse1/Kap121 and exportin Msn5. These data demonstrate the utility of FRET in mapping dynamic protein interactions in a genetic system. Furthermore, the data indicate that an importin and exportin have overlapping pathways through the NPC.
引用
收藏
页码:133 / 140
页数:8
相关论文
共 34 条
  • [1] NUP1 MUTANTS EXHIBIT PLEIOTROPIC DEFECTS IN NUCLEAR-PORE COMPLEX FUNCTION
    BOGERD, AM
    HOFFMAN, JA
    AMBERG, DC
    FINK, GR
    DAVIS, LI
    [J]. JOURNAL OF CELL BIOLOGY, 1994, 127 (02) : 319 - 332
  • [2] Clegg R. M, 1996, Fluorescence Imaging Spectroscopy and Microscopy
  • [3] Nucleocytoplasmic transport of macromolecules
    Corbett, AH
    Silver, PA
    [J]. MICROBIOLOGY AND MOLECULAR BIOLOGY REVIEWS, 1997, 61 (02) : 193 - +
  • [4] RNA1P, A RAN/TC4 GTPASE-ACTIVATING PROTEIN, IS REQUIRED FOR NUCLEAR IMPORT
    CORBETT, AH
    KOEPP, DM
    SCHLENSTEDT, G
    LEE, MS
    HOPPER, AK
    SILVER, PA
    [J]. JOURNAL OF CELL BIOLOGY, 1995, 130 (05) : 1017 - 1026
  • [5] Visualization of Pit-1 transcription factor interactions in the living cell nucleus by fluorescence resonance energy transfer microscopy
    Day, RN
    [J]. MOLECULAR ENDOCRINOLOGY, 1998, 12 (09) : 1410 - 1419
  • [6] Yeast genetics to dissect the nuclear pore complex and nucleocytoplasmic trafficking
    Fabre, E
    Hurt, E
    [J]. ANNUAL REVIEW OF GENETICS, 1997, 31 : 277 - 313
  • [7] Molecular architecture of the yeast nuclear pore complex:: Localization of Nsp1p subcomplexes
    Fahrenkrog, B
    Hurt, EC
    Aebi, U
    Panté, N
    [J]. JOURNAL OF CELL BIOLOGY, 1998, 143 (03) : 577 - 588
  • [8] Quantitative fluorescence resonance energy transfer measurements using fluorescence microscopy
    Gordon, GW
    Berry, G
    Liang, XH
    Levine, B
    Herman, B
    [J]. BIOPHYSICAL JOURNAL, 1998, 74 (05) : 2702 - 2713
  • [9] 2 DIFFERENT SUBUNITS OF IMPORTIN COOPERATE TO RECOGNIZE NUCLEAR-LOCALIZATION SIGNALS AND BIND THEM TO THE NUCLEAR-ENVELOPE
    GORLICH, D
    KOSTKA, S
    KRAFT, R
    DINGWALL, C
    LASKEY, RA
    HARTMANN, E
    PREHN, S
    [J]. CURRENT BIOLOGY, 1995, 5 (04) : 383 - 392
  • [10] FUNCTIONAL INTERACTION OF NIC96P WITH A CORE NUCLEOPORIN COMPLEX CONSISTING OF NSP1P, NUP49P AND A NOVEL PROTEIN NUP57P
    GRANDI, P
    SCHLAICH, N
    TEKOTTE, H
    HURT, EC
    [J]. EMBO JOURNAL, 1995, 14 (01) : 76 - 87