Dynamic properties of nuclear pore complex proteins in gp210 deficient cells

被引:25
作者
Eriksson, C
Rustum, C
Hallberg, E [1 ]
机构
[1] Sodertorns Univ Coll, Sect Nat Sci, S-14189 Huddinge, Sweden
[2] Karolinska Inst, Ctr Biotechnol, S-14157 Huddinge, Sweden
[3] Stockholm Univ, Dept Neurochem & Neurotoxicol, S-10691 Stockholm, Sweden
来源
FEBS LETTERS | 2004年 / 572卷 / 1-3期
关键词
nuclear pore complex; nucleoporin; integral membrane protein; fluorescence recovery after photobleaching;
D O I
10.1016/j.febslet.2004.07.044
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
Gp210, an integral membrane protein of the nuclear pore complex (NPC), is believed to be involved in NPC biogenesis. To test this hypothesis, we have investigated dynamic properties of the NPC and distribution of NPC proteins in NIH/ 3T3 cells lacking gp210. POM121 (the other integral NPC protein) and NUP107 (of the NUP107/160 complex) were correctly distributed at the nuclear pores in the absence of gp210. Furthermore, fluorescence recovery after photobleaching experiments showed that POM121 and NUP107 remained stably associated at the NPCs. We conclude that gp210 cannot be required for incorporation of POM121 or NUP107 or be required for maintaining NPC stability. (C) 2004 Published by Elsevier B.V. on behalf of the Federation of European Biochemical Societies.
引用
收藏
页码:261 / 265
页数:5
相关论文
共 23 条
  • [1] An evolutionarily conserved NPC subcomplex, which redistributes in part to kinetochores in mammalian cells
    Belgareh, N
    Rabut, G
    Baï, SW
    van Overbeek, M
    Beaudouin, J
    Daigle, N
    Zatsepina, OV
    Pasteau, F
    Labas, V
    Fromont-Racine, M
    Ellenberg, J
    Doye, V
    [J]. JOURNAL OF CELL BIOLOGY, 2001, 154 (06) : 1147 - 1160
  • [2] Bodoor K, 1999, J CELL SCI, V112, P2253
  • [3] Nuclear pore protein gp210 is essential for viability in HeLa cells and Caenorhabditis elegans
    Cohen, M
    Feinstein, N
    Wilson, KL
    Gruenbaum, Y
    [J]. MOLECULAR BIOLOGY OF THE CELL, 2003, 14 (10) : 4230 - 4237
  • [4] Proteomic analysis of the mammalian nuclear pore complex
    Cronshaw, JA
    Krutchinsky, AN
    Zhang, WZ
    Chait, BT
    Matunis, MJ
    [J]. JOURNAL OF CELL BIOLOGY, 2002, 158 (05) : 915 - 927
  • [5] Nuclear pore complexes form immobile networks and have a very low turnover in live mammalian cells
    Daigle, N
    Beaudouin, J
    Hartnell, L
    Imreh, G
    Hallberg, E
    Lippincott-Schwartz, J
    Ellenberg, J
    [J]. JOURNAL OF CELL BIOLOGY, 2001, 154 (01) : 71 - 84
  • [6] IDENTIFICATION AND CHARACTERIZATION OF A NUCLEAR-PORE COMPLEX PROTEIN
    DAVIS, LI
    BLOBEL, G
    [J]. CELL, 1986, 45 (05) : 699 - 709
  • [7] Interference with the cytoplasmic tail of gp210 disrupts "close apposition" of nuclear membranes and blocks nuclear pore dilation
    Drummond, SP
    Wilson, KL
    [J]. JOURNAL OF CELL BIOLOGY, 2002, 158 (01) : 53 - 62
  • [8] The nuclear pore complex:: a jack of all trades?
    Fahrenkrog, B
    Köser, J
    Aebi, U
    [J]. TRENDS IN BIOCHEMICAL SCIENCES, 2004, 29 (04) : 175 - 182
  • [9] Biochemical characterization of nuclear pore complex protein gp210 oligomers
    Favreau, C
    Bastos, R
    Cartaud, J
    Courvalin, JC
    Mustonen, P
    [J]. EUROPEAN JOURNAL OF BIOCHEMISTRY, 2001, 268 (14): : 3883 - 3889
  • [10] Caenorhabditis elegans nucleoporins Nup93 and Nup205 determine the limit of nuclear pore complex size exclusion in vivo
    Galy, V
    Mattaj, IW
    Askjaer, P
    [J]. MOLECULAR BIOLOGY OF THE CELL, 2003, 14 (12) : 5104 - 5115