Modulation of nuclear protein import - A novel means of regulating gene expression

被引:17
作者
Fujihara, SM [1 ]
Nadler, SG [1 ]
机构
[1] Bristol Myers Squibb Pharmaceut Res Inst, Princeton, NJ 08543 USA
关键词
nuclear transport; peptides; karyopherin alpha; NLS;
D O I
10.1016/S0006-2952(98)00049-5
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Eukaryotic cells depend upon the regulated exchange of proteins and RNA between, the cytoplasm and the nucleus far survival. Various cytoplasmic and nuclear proteins play a fundamental role in this specific transport process. Over the last few years the components and stages of nuclear protein transport have been characterized in significant detail. Because many of the proteins that are transported into the nucleus are transcription factors, the import process is an interesting target for the manipulation of gene expression. Over time the eukaryotic cell has assembled a number of methods by which to regulate the nuclear localization of transcription factors. Within the last few years, there have been several reports of the pharmacologic manipulation of the localization of nuclear proteins as well. In addition, a recent study suggests that viruses are able to modulate host cell nuclear protein transport in vivo. This report will present an overview of nuclear protein import, describe the various in vivo mechanisms by which the cell regulates this process; and discuss recent attempts to manipulate the process with small molecule compounds. As nuclear import isa fundamental cellular process, potential opportunities for the future may arise from direct and specific ways to modulate this process and thereby treat diseases characterized by dysregulation of transcription factor activity. (C) 1998 Elsevier Science Inc.
引用
收藏
页码:157 / 161
页数:5
相关论文
共 40 条
[1]   IDENTIFICATION OF SPECIFIC BINDING-PROTEINS FOR A NUCLEAR LOCATION SEQUENCE [J].
ADAM, SA ;
LOBL, TJ ;
MITCHELL, MA ;
GERACE, L .
NATURE, 1989, 337 (6204) :276-279
[2]   NUCLEAR-PROTEIN IMPORT IN PERMEABILIZED MAMMALIAN-CELLS REQUIRES SOLUBLE CYTOPLASMIC FACTORS [J].
ADAM, SA ;
MARR, RS ;
GERACE, L .
JOURNAL OF CELL BIOLOGY, 1990, 111 (03) :807-816
[3]   Mechanisms of disease - Nuclear factor-kappa b - A pivotal transcription factor in chronic inflammatory diseases [J].
Barnes, PJ ;
Larin, M .
NEW ENGLAND JOURNAL OF MEDICINE, 1997, 336 (15) :1066-1071
[4]  
Boulikas Teni, 1993, Critical Reviews in Eukaryotic Gene Expression, V3, P193
[5]   How structural features influence the biomembrane permeability of peptides [J].
Burton, PS ;
Conradi, RA ;
Ho, NFH ;
Hilgers, AR ;
Borchardt, RT .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1996, 85 (12) :1336-1340
[6]   SEQUENCE REQUIREMENTS FOR SYNTHETIC PEPTIDE-MEDIATED TRANSLOCATION TO THE NUCLEUS [J].
CHELSKY, D ;
RALPH, R ;
JONAK, G .
MOLECULAR AND CELLULAR BIOLOGY, 1989, 9 (06) :2487-2492
[7]   Protein transport: The nonclassical ins and outs [J].
Cleves, AE .
CURRENT BIOLOGY, 1997, 7 (05) :R318-R320
[8]   NUCLEAR-LOCALIZATION SIGNAL OF HIV-1 AS A NOVEL TARGET FOR THERAPEUTIC INTERVENTION [J].
DUBROVSKY, L ;
ULRICH, P ;
NUOVO, GJ ;
MANOGUE, KR ;
CERAMI, A ;
BUKRINSKY, M .
MOLECULAR MEDICINE, 1995, 1 (02) :217-230
[9]   SYNTHETIC PEPTIDES AS NUCLEAR-LOCALIZATION SIGNALS [J].
GOLDFARB, DS ;
GARIEPY, J ;
SCHOOLNIK, G ;
KORNBERG, RD .
NATURE, 1986, 322 (6080) :641-644
[10]   Protein kinesis - Nucleocytoplasmic transport [J].
Gorlich, D ;
Mattaj, IW .
SCIENCE, 1996, 271 (5255) :1513-1518