The hnRNP C proteins contain a nuclear retention sequence that can override nuclear export signals

被引:186
作者
Nakielny, S [1 ]
Dreyfuss, G [1 ]
机构
[1] UNIV PENN,SCH MED,HOWARD HUGHES MED INST,DEPT BIOCHEM & BIOPHYS,PHILADELPHIA,PA 19104
关键词
D O I
10.1083/jcb.134.6.1365
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Nascent pre-mRNAs associate with the abundant heterogeneous nuclear RNP (hnRNP) proteins and remain associated with them throughout the time they are in the nucleus. The hnRNP proteins can be divided into two groups according to their nucleocytoplasmic transport properties. One group is completely restricted to the nucleus in interphase cells, whereas the other group, although primarily nuclear at steady state, shuttles between the nucleus and the cytoplasm. Nuclear export of the shuttling hnRNP proteins is mediated by nuclear export signals (NESs). Mounting evidence indicates that NES-bearing hnRNP proteins are mediators of mRNA export. The hnRNP C proteins are representative of the nonshuttling group of hnRNP proteins. Here we show that hnRNP C proteins are restricted to the nucleus not because they lack an NES, but because they bear a nuclear retention sequence (NRS) that is capable of overriding NESs. The NRS comprises similar to 78 amino acids and is largely within the auxiliary domain of hnRNP C1. We suggest that the removal of NRS-containing hnRNP proteins from pre-mRNA/mRNA is required for mRNA export from the nucleus and is an essential step in the pathway of gene expression.
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页码:1365 / 1373
页数:9
相关论文
共 42 条
  • [1] Boulikas Teni, 1993, Critical Reviews in Eukaryotic Gene Expression, V3, P193
  • [2] CONSERVED STRUCTURES AND DIVERSITY OF FUNCTIONS OF RNA-BINDING PROTEINS
    BURD, CG
    DREYFUSS, G
    [J]. SCIENCE, 1994, 265 (5172) : 615 - 621
  • [3] PRIMARY STRUCTURES OF THE HETEROGENEOUS NUCLEAR RIBONUCLEOPROTEIN A2-PROTEIN, B1-PROTEIN, AND C2-PROTEIN - A DIVERSITY OF RNA-BINDING PROTEINS IS GENERATED BY SMALL PEPTIDE INSERTS
    BURD, CG
    SWANSON, MS
    GORLACH, M
    DREYFUSS, G
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (24) : 9788 - 9792
  • [4] ALTERNATIVE SPLICING IN THE HUMAN GENE FOR THE CORE PROTEIN-A1 GENERATES ANOTHER HNRNP PROTEIN
    BUVOLI, M
    COBIANCHI, F
    BESTAGNO, MG
    MANGIAROTTI, A
    BASSI, MT
    BIAMONTI, G
    RIVA, S
    [J]. EMBO JOURNAL, 1990, 9 (04) : 1229 - 1235
  • [5] REGULATION OF ALTERNATIVE SPLICING IN-VIVO BY OVEREXPRESSION OF ANTAGONISTIC SPLICING FACTORS
    CACERES, JF
    STAMM, S
    HELFMAN, DM
    KRAINER, AR
    [J]. SCIENCE, 1994, 265 (5179) : 1706 - 1709
  • [6] REGULATION BY HIV REV DEPENDS UPON RECOGNITION OF SPLICE SITES
    CHANG, DD
    SHARP, PA
    [J]. CELL, 1989, 59 (05) : 789 - 795
  • [7] HETEROGENEOUS NUCLEAR RIBONUCLEOPROTEINS - ROLE IN RNA SPLICING
    CHOI, YD
    GRABOWSKI, PJ
    SHARP, PA
    DREYFUSS, G
    [J]. SCIENCE, 1986, 231 (4745) : 1534 - 1539
  • [8] RCH1, A PROTEIN THAT SPECIFICALLY INTERACTS WITH THE RAG-1 RECOMBINATION-ACTIVATING PROTEIN
    CUOMO, CA
    KIRCH, SA
    GYURIS, J
    BRENT, R
    OETTINGER, MA
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (13) : 6156 - 6160
  • [9] NUCLEAR TARGETING SEQUENCES - A CONSENSUS
    DINGWALL, C
    LASKEY, RA
    [J]. TRENDS IN BIOCHEMICAL SCIENCES, 1991, 16 (12) : 478 - 481
  • [10] HNRNP PROTEINS AND THE BIOGENESIS OF MESSENGER-RNA
    DREYFUSS, G
    MATUNIS, MJ
    PINOLROMA, S
    BURD, CG
    [J]. ANNUAL REVIEW OF BIOCHEMISTRY, 1993, 62 : 289 - 321