A novel complex of nucleoporins, which includes Sec13p and a Sec13p homolog, is essential for normal nuclear pores

被引:270
作者
Siniossoglou, S
Wimmer, C
Rieger, M
Doye, V
Tekotte, H
Weise, C
Emig, S
Segref, A
Hurt, EC
机构
[1] EUROPEAN MOLEC BIOL LAB, D-69115 HEIDELBERG, GERMANY
[2] FREE UNIV BERLIN, INST BIOCHEM, D-14195 BERLIN, GERMANY
[3] GENOTYPE GMBH, D-69259 WILHELMSFELD, GERMANY
[4] INST CURIE, CNRS UMR 144, SECT RECH, F-75231 PARIS, FRANCE
关键词
D O I
10.1016/S0092-8674(00)80981-2
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
In a genetic screen for nucleoporin-interacting components, a novel nuclear pore protein Nup84p, which exhibits homology to mammalian Nup107p, was isolated. Nup84p forms a complex with five proteins, of which Nup120p, Nup85p, Sec13p, and a Sec13p homolog were identified. Upon isolation of Sec13p-ProtA, nucleoporins were still associated, but the major copurifying band was a 150 kDa protein, showing that Sec13p occurs in two complexes. Disruption of any of the genes encoding Nup84p, Nup85p, or Nup120p caused defects in nuclear membrane and nuclear pore complex organization, as well as in poly(A)(+) RNA transport. Thus, the Nup84p complex in conjunction with Sec13-type proteins is required for correct nuclear pore biogenesis.
引用
收藏
页码:265 / 275
页数:11
相关论文
共 33 条
  • [1] ISOLATION AND CHARACTERIZATION OF RAT1 - AN ESSENTIAL GENE OF SACCHAROMYCES-CEREVISIAE REQUIRED FOR THE EFFICIENT NUCLEOCYTOPLASMIC TRAFFICKING OF MESSENGER-RNA
    AMBERG, DC
    GOLDSTEIN, AL
    COLE, CN
    [J]. GENES & DEVELOPMENT, 1992, 6 (07) : 1173 - 1189
  • [2] COPII - A MEMBRANE COAT FORMED BY SEC PROTEINS THAT DRIVE VESICLE BUDDING FROM THE ENDOPLASMIC-RETICULUM
    BARLOWE, C
    ORCI, L
    YEUNG, T
    HOSOBUCHI, M
    HAMAMOTO, S
    SALAMA, N
    REXACH, MF
    RAVAZZOLA, M
    AMHERDT, M
    SCHEKMAN, R
    [J]. CELL, 1994, 77 (06) : 895 - 907
  • [3] 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
  • [4] IDENTIFICATION OF A SOLUBLE PRECURSOR COMPLEX ESSENTIAL FOR NUCLEAR-PORE ASSEMBLY INVITRO
    DABAUVALLE, MC
    LOOS, K
    SCHEER, U
    [J]. CHROMOSOMA, 1990, 100 (01) : 56 - 66
  • [5] GENETIC APPROACHES TO NUCLEAR-PORE STRUCTURE AND FUNCTION
    DOYE, V
    HURT, EC
    [J]. TRENDS IN GENETICS, 1995, 11 (06) : 235 - 241
  • [6] A NOVEL NUCLEAR-PORE PROTEIN NUP133P WITH DISTINCT ROLES IN POLY(A)(+) RNA TRANSPORT AND NUCLEAR-PORE DISTRIBUTION
    DOYE, V
    WEPF, R
    HURT, EC
    [J]. EMBO JOURNAL, 1994, 13 (24) : 6062 - 6075
  • [7] A COMPLEX OF NUCLEAR-PORE PROTEINS REQUIRED FOR PORE FUNCTION
    FINLAY, DR
    MEIER, E
    BRADLEY, P
    HORECKA, J
    FORBES, DJ
    [J]. JOURNAL OF CELL BIOLOGY, 1991, 114 (01) : 169 - 183
  • [8] RECONSTITUTION OF BIOCHEMICALLY ALTERED NUCLEAR-PORES - TRANSPORT CAN BE ELIMINATED AND RESTORED
    FINLAY, DR
    FORBES, DJ
    [J]. CELL, 1990, 60 (01) : 17 - 29
  • [9] A CONDITIONAL ALLELE OF THE NOVEL REPEAT-CONTAINING YEAST NUCLEOPORIN RAT7 NUP159 CAUSES BOTH RAPID CESSATION OF MESSENGER-RNA EXPORT AND REVERSIBLE CLUSTERING OF NUCLEAR-PORE COMPLEXES
    GORSCH, LC
    DOCKENDORFF, TC
    COLE, CN
    [J]. JOURNAL OF CELL BIOLOGY, 1995, 129 (04) : 939 - 955
  • [10] PURIFICATION OF NSP1 REVEALS COMPLEX-FORMATION WITH GLFG NUCLEOPORINS AND A NOVEL NUCLEAR-PORE PROTEIN NIC96
    GRANDI, P
    DOYE, V
    HURT, EC
    [J]. EMBO JOURNAL, 1993, 12 (08) : 3061 - 3071