Nucleocytoplasmic transport of macromolecules

被引:172
作者
Corbett, AH
Silver, PA
机构
[1] DANA FARBER CANC INST, DIV CELLULAR & MOL BIOL, BOSTON, MA 02115 USA
[2] HARVARD UNIV, SCH MED, DEPT BIOL CHEM & MOL PHARMACOL, BOSTON, MA 02115 USA
关键词
D O I
10.1128/.61.2.193-211.1997
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Nucleocytoplasmic transport is a complex process that consists of the movement of numerous macromolecules back and forth across the nuclear envelope. All macromolecules that move in and out of the nucleus do so via nuclear pore complexes that fern? large proteinaceous channels in the nuclear envelope. In addition to nuclear-pores, nuclear transport of macromolecules requires a number of soluble factors that are found both in the cytoplasm and in the nucleus. A combination of biochemical, genetic, and cell biological approaches have been used to identify and characterize the various components of the nuclear transport machinery. Recent studies have shown that both import to and export from the nucleus are mediated by signals found within the transport substrates. Several studies have demonstrated that these signals are recognized by soluble factors that target these substrates to the nuclear pore. Once substrates have been directed to the pore, most transport events depend on a cycle of GTP hydrolysis mediated by the small Ras-like GTPase, Ran as well as other proteins that regulate the guanine nucleotide-bound state of Ran. Many of the essential factors have been identified, and the challenge that remains is to determine the exact mechanism by which transport occurs. This review attempts to present an integrated view of our current understanding of nuclear transport while highlighting the contributions that have been made through studies with genetic organisms such as the budding yeast, Saccharomyces cerevisiae.
引用
收藏
页码:193 / +
页数:1
相关论文
共 281 条
[31]   A MUTANT NUCLEAR-PROTEIN WITH SIMILARITY TO RNA-BINDING PROTEINS INTERFERES WITH NUCLEAR IMPORT IN YEAST [J].
BOSSIE, MA ;
DEHORATIUS, C ;
BARCELO, G ;
SILVER, P .
MOLECULAR BIOLOGY OF THE CELL, 1992, 3 (08) :875-893
[32]  
BOURNE HR, 1991, NATURE, V349, P117, DOI 10.1038/349117a0
[33]   JAKs and STATs branch out [J].
Briscoe, J ;
Kohlhuber, F ;
Muller, M .
TRENDS IN CELL BIOLOGY, 1996, 6 (09) :336-340
[34]   A MUTATION IN THE SCHIZOSACCHAROMYCES-POMBE RAE1 GENE CAUSES DEFECTS IN POLY(A)(+) RNA EXPORT AND IN THE CYTOSKELETON [J].
BROWN, JA ;
BHARATHI, A ;
GHOSH, A ;
WHALEN, W ;
FITZGERALD, E ;
DHAR, R .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (13) :7411-7419
[35]   The 1.6 angstrom resolution crystal structure of nuclear transport factor 2 (NTF2) [J].
Bullock, TL ;
Clarkson, WD ;
Kent, HM ;
Stewart, M .
JOURNAL OF MOLECULAR BIOLOGY, 1996, 260 (03) :422-431
[36]   TPR, A LARGE COILED-COIL PROTEIN WHOSE AMINO-TERMINUS IS INVOLVED IN ACTIVATION OF ONCOGENIC KINASES, IS LOCALIZED TO THE CYTOPLASMIC SURFACE OF THE NUCLEAR-PORE COMPLEX [J].
BYRD, DA ;
SWEET, DJ ;
PANTE, N ;
KONSTANTINOV, KN ;
GUAN, TL ;
SAPHIRE, ACS ;
MITCHELL, PJ ;
COOPER, CS ;
AEBI, U ;
GERACE, L .
JOURNAL OF CELL BIOLOGY, 1994, 127 (06) :1515-1526
[37]   Evidence using a green fluorescent protein-glucocorticoid receptor chimera that the RAN/TC4 GTPase mediates an essential function independent of nuclear protein import [J].
Carey, KL ;
Richards, SA ;
Lounsbury, KM ;
Macara, IG .
JOURNAL OF CELL BIOLOGY, 1996, 133 (05) :985-996
[38]   ACROSS THE NUCLEAR-PORES WITH THE HELP OF NUCLEOPORINS [J].
CARMOFONSECA, M ;
HURT, EC .
CHROMOSOMA, 1991, 101 (04) :199-205
[39]   GTPASE CASCADES CHOREOGRAPHING CELLULAR BEHAVIOR - MOVEMENT, MORPHOGENESIS, AND MORE [J].
CHANT, J ;
STOWERS, L .
CELL, 1995, 81 (01) :1-4
[40]   DIVERSE EFFECTS OF THE GUANINE-NUCLEOTIDE EXCHANGE FACTOR RCC1 ON RNA TRANSPORT [J].
CHENG, Y ;
DAHLBERG, JE ;
LUND, E .
SCIENCE, 1995, 267 (5205) :1807-1810